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Last Updated :2024/10/24

研究者情報

マスター

アカウント（マスター）

  • 氏名

    北村　朗(キタムラ　アキラ), キタムラ　アキラ

所属（マスター）

  • 先端生命科学研究院　生命機能科学研究部門　細胞機能科学分野

所属（マスター）

  • 先端生命科学研究院　生命機能科学研究部門　細胞機能科学分野

独自項目

syllabus

  • 2021, 大学院共通授業科目（教育プログラム）：脳科学研究の展開, Inter-Graduate School Classes(Educational Program):Brain Science Research, 修士課程, 大学院共通科目, 脳科学，生命科学，方法論，脳機能計測
  • 2021, 大学院共通授業科目（一般科目）：自然科学・応用科学, Inter-Graduate School Classes(General Subject):Natural and Applied Sciences, 修士課程, 大学院共通科目, Optical microscopy, Confocal Laser Scanning Microscopy, Fluorescence Correlation Spectroscopy，Fluorescence Cross-Correlation Spectroscopy，Super-resolution Optical Microscopy, Bioimaging, Live Cell imaging, FRAP, Quantitative Cell Biology, Biophysics
  • 2021, 大学院共通授業科目（一般科目）：自然科学・応用科学, Inter-Graduate School Classes(General Subject):Natural and Applied Sciences, 修士課程, 大学院共通科目, Optical microscopy, laser scanning microscopy, confocal microscopy, fluorescence correlation spectroscopy，image correlation spectroscopy，bioimaging, live cell imaging, Cell biology, Biophysics, GFP, Single plane illumination,
  • 2021, 生命科学特別講義Ⅲ, Life Science Special Lecture III, 修士課程, 生命科学院, 光学顕微鏡、レーザー走査顕微鏡、共焦点顕微鏡、蛍光相関分光法、蛍光相互相関分光法，超解像顕微鏡，バイオイメージング
  • 2021, 生命科学特別講義Ⅲ, Life Science Special Lecture III, 修士課程, 生命科学院, 光学顕微鏡, 蛍光相関分光法、蛍光相互相関分光法，超解像顕微鏡，バイオイメージング，拡散定数。　分子数
  • 2021, 大学院共通授業科目（一般科目）：自然科学・応用科学, Inter-Graduate School Classes(General Subject):Natural and Applied Sciences, 修士課程, 大学院共通科目, Optical microscopy, Confocal Laser Scanning Microscopy, Fluorescence Correlation Spectroscopy，Fluorescence Cross-Correlation Spectroscopy，Super-resolution Optical Microscopy, Bioimaging, Live Cell imaging, FRAP, Quantitative Cell Biology, Biophysics, GFP, Diffusion, Diffusion constant,
  • 2021, 生物系の反応速度論, Reaction Kinetics for Life Science, 学士課程, 理学部, 反応速度の定義，反応速度式，反応のダイナミクス，拡散律速の反応，遷移状態理論，固体表面への吸着過程，生体内化学反応の取り扱い
  • 2021, 細胞構造科学Ⅲ, Cell Structural Science III, 学士課程, 理学部, 細胞骨格、モータータンパク質、筋収縮、細胞周期、細胞分裂、染色体の複製・分配、紡錘体、がん、代謝、生合成、生体内酸化還元反応、光合成、オルガネラの起源
  • 2021, 生体高分子学実験Ⅱ, Laboratory Work on Bio-macromolecular Science II, 学士課程, 理学部, 物理学実験，化学分析実験，有機合成実験，生化学実験, 分子生物学実験，細胞生物学実験, 生物物理学実験
  • 2021, 実験生物科学, Experimental Biological Science, 学士課程, 理学部, 高分子機能学，実験技術，生命科学，物質科学，情報科学，融合科学
  • 2021, 高分子機能学基礎実験, Fundamental Laboratory Work on Bio-macromolecular Science, 学士課程, 理学部, 基礎実験手法，物理学実験，化学分析実験，有機合成実験，生化学実験，安全教育，法令

researchmap

プロフィール情報

学位

  • 修士（理学）（2005年03月 京都大学）
  • 博士（理学）（2008年03月 京都大学）

プロフィール情報

  • 姓

    北村, キタムラ

  • 名

    朗, アキラ

  • ID各種

    200901073020874800

業績リスト

研究キーワード

  • TRAST monitoring   シャペロンRNA   プロテオスタシス   FRAP   蛍光共鳴エネルギー移動   蛍光相関分光法   筋萎縮性側索硬化症   タンパク質恒常性   生細胞イメージング   神経変性疾患   分子シャペロン   タンパク質フォールディング   タンパク質凝集体   

研究分野

  • ライフサイエンス / 機能生物化学
  • ライフサイエンス / 生物物理学
  • ライフサイエンス / 分子生物学
  • ライフサイエンス / 細胞生物学

経歴

  • 2024年09月 - 現在 北海道大学 大学院先端生命科学研究院 准教授 (PI)
  • 2023年08月 - 現在 特定国立研究開発法人理化学研究所 生命機能科学研究センター 客員研究員
  • 2022年10月 - 現在 PRIME, AMED
  • 2019年10月 - 現在 北海道大学 脳科学研究教育センター 基幹教員
  • 2023年08月 - 2024年08月 北海道大学 大学院先端生命科学研究院 講師（テニュア・PI）
  • 2019年04月 - 2023年07月 北海道大学 大学院先端生命科学研究院 講師（テニュアトラック）
  • 2017年 - 2020年03月 JSPS 国際共同研究加速基金研究者
  • 2010年04月 - 2019年03月 北海道大学 大学院先端生命科学研究院 助教
  • 2018年08月 - 2018年11月 ノースウェスタン大学 Prof. Richard Morimoto Laboratory Visiting Scholar
  • 2018年05月 - 2018年06月 スウェーデン王立工科大学 応用物理学部 JSPS 国際共同研究強化基金研究者
  • 2017年10月 - 2017年12月 スウェーデン王立工科大学 応用物理学部 JSPS 国際共同研究強化基金研究者
  • 2008年04月 - 2010年03月 北海道大学 大学院 先端生命科学研究院 細胞機能科学分野 日本学術振興会特別研究員PD
  • 2006年04月 - 2008年03月 京都大学再生医科学研究所 細胞機能調節学分野 日本学術振興会特別研究員 (DC2)

学歴

  •         - 2008年   京都大学   大学院理学研究科   生物科学専攻 博士課程修了
  •         - 2008年   京都大学
  •         - 2005年   京都大学   大学院理学研究科   生物科学専攻 修士課程修了
  •         - 2003年   京都大学   工学部   工業化学科
  •         - 2003年   京都大学

委員歴

  • 2024年02月 - 現在   Frontiers in Biophysics   Review editor
  • 2024年01月 - 現在   Biophysics and Physicobiology (BPPB)   Editorial Board Members
  • 2023年 - 現在   Spectroscopy Journal   Editorial Board Members
  • 2018年01月 - 現在   日本生物物理学会   分野別専門委員（神経変性疾患分野）
  • 2009年 - 現在   光イメージング若手の会「光塾」   総括塾員
  • 2023年 - 2023年   第32回 日本バイオイメージング学会学術集会   実行委員
  • 2022年 - 2022年   日本生物物理学会   第60回年会 実行委員
  • 2012年04月 - 2015年03月   日本生物物理学会   分野別専門委員（タンパク質の品質管理）
  • 2014年 - 2014年   日本生物物理学会第52回年会   実行委員

受賞

  • 2022年09月 日本生物物理学会 第11回Biophysics and Physicobiology論文賞
     
    受賞者: 北村朗

論文

  • Ai Fujimoto, Masataka Kinjo, Akira Kitamura
    JACS Au 2024年09月23日 [査読有り][通常論文]
  • Ai Fujimoto, Haruki Kawai, Rintaro Kawamura, Akira Kitamura
    Cells 13 16 1318  2024年08月07日 [査読有り][通常論文]
  • Akira Kitamura, Ai Fujimoto, Rei Kawashima, Yidan Lyu, Kotetsu Sasaki, Yuta Hamada, Kanami Moriya, Ayumi Kurata, Kazuho Takahashi, Reneé Brielmann, Laura C. Bo, Richard I. Morimoto, Masataka Kinjo
    Communications Biology 7 1 743  2024年06月20日 [査読有り][通常論文]
     
    Abstract Carboxy terminal fragments (CTFs) of TDP-43 contain an intrinsically disordered region (IDR) and form cytoplasmic condensates containing amyloid fibrils. Such condensates are toxic and associated with pathogenicity in amyotrophic lateral sclerosis. However, the molecular details of how the domain of TDP-43 CTFs leads to condensation and cytotoxicity remain elusive. Here, we show that truncated RNA/DNA-recognition motif (RRM) at the N-terminus of TDP-43 CTFs leads to the structural transition of the IDR, whereas the IDR itself of TDP-43 CTFs is difficult to assemble even if they are proximate intermolecularly. Hetero-oligomers of TDP-43 CTFs that have recruited other proteins are more toxic than homo-oligomers, implicating loss-of-function of the endogenous proteins by such oligomers is associated with cytotoxicity. Furthermore, such toxicity of TDP-43 CTFs was cell-nonautonomously affected in the nematodes. Therefore, misfolding and oligomeric characteristics of the truncated RRM at the N-terminus of TDP-43 CTFs define their condensation properties and toxicity.
  • Takumi Koizumi, Ai Fujimoto, Haruka Kawaguchi, Tsumugi Kurosaki, Akira Kitamura
    ACS Omega 2024年05月14日 [査読有り][通常論文]
  • Yuzuha Shiraki, Monet Mitsuma, Ritsuko Takada, Saori Hata, Akira Kitamura, Shinji Takada, Masataka Kinjo, Hidenori Taru, Ulrike C Müller, Tohru Yamamoto, Yuriko Sobu, Toshiharu Suzuki
    Molecular biology of the cell 34 11 ar110  2023年10月01日 [査読有り]
     
    Alcadein α (Alcα) and amyloid-β protein precursor (APP) are cargo receptors that associate vesicles with kinesin-1. These vesicles, which contain either Alcα or APP, transport various proteins/cargo molecules into axon nerve terminals. Here, we analyzed immune-isolated Alcα- and APP-containing vesicles of adult mouse brains with LC-MS/MS and identified proteins present in vesicles that contained either Alcα or APP. Among these proteins, Frizzled-5 (Fzd5), a Wnt receptor, was detected mainly in Alcα vesicles. Although colocalization ratios of Fzd5 with Alcα are low in the neurites of differentiating neurons by a low expression of Fzd5 in embryonic brains, the suppression of Alcα expression decreased the localization of Fzd5 in neurites of primary cultured neurons. Furthermore, Fzd5-EGFP expressed in primary cultured neurons was preferentially transported in axons with the transport velocities of Alcα vesicles. In synaptosomal fractions of adult-mice brains that express higher levels of Fzd5, the amount of Fzd5 and the phosphorylation level of calcium/calmodulin-dependent protein kinase-II were reduced in the Alcα-deficient mice. These results suggest that reduced transport of Fzd5 by Alcα-containing vesicles associated with kinesin-1 in axon terminals may impair the response to Wnt ligands in the noncanonical Ca2+-dependent signal transduction pathway at nerve terminals of mature neurons.
  • Akira Kitamura, Sho Oasa, Haruka Kawaguchi, Misato Osaka, Vladana Vukojević, Masataka Kinjo
    Scientific reports 13 1 11834 - 11834 2023年07月22日 [査読有り][通常論文]
     
    Hyperosmotic stress activates in live cells numerous processes and also promotes intracellular protein/RNA aggregation and phase separation. However, the time course and the extent of these changes remain largely uncharacterized. To investigate dynamic changes in intracellular macromolecular crowding (MMC) induced by hyperosmotic stress in live cells, we used fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy (FCS) to quantify changes in the local environment by measuring the fluorescence lifetime and the diffusion of the monomeric enhanced green fluorescent protein (eGFP), respectively. Real-time monitoring of eGFP fluorescence lifetime showed that a faster response to environmental changes due to MMC is observed than when measuring the acceptor/donor emission ratio using the MMC-sensitive Förster resonance energy transfer sensor (GimRET). This suggests that eGFP molecular electronic states and/or collision frequency are affected by changes in the immediate surroundings due to MMC without requiring conformational changes as is the case for the GimRET sensor. Furthermore, eGFP diffusion assessed by FCS indicated higher intracellular viscosity due to increased MMC during hyperosmotic stress. Our findings reveal that changes in eGFP fluorescence lifetime and diffusion are early indicators of elevated intracellular MMC. Our approach can therefore be used to reveal in live cells short-lived transient states through which MMC builds over time, which could not be observed when measuring changes in other physical properties that occur at slower time scales.
  • Yuta Hamada, Akira Kitamura
    Spectroscopy Journal 2023年07月10日 [査読有り][通常論文]
  • Akira Kitamura, Johan Tornmalm, Baris Demirbay, Joachim Piguet, Masataka Kinjo, Jerker Widengren
    Nucleic Acids Research 2023年03月21日 [査読有り][通常論文]
  • Akira Kitamura, Sachiko Yuno, Rintaro Kawamura, Masataka Kinjo
    International Journal of Molecular Sciences 24 6 5513  2023年03月14日 [査読有り][通常論文]
  • Akira Kitamura, Ryo Iizuka
    Biophysics and Physicobiology 2022年 [査読有り][招待有り]
  • Ai Fujimoto, Yidan Lyu, Masataka Kinjo, Akira Kitamura
    Applied Sciences 11 22 10697 - 10697 2021年11月12日 [査読有り][招待有り]
     
    Infection with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the cause of coronavirus disease 2019 (COVID-19), is initiated by the interaction between a receptor protein, angiotensin-converting enzyme type 2 (ACE2) on the cell surface, and the viral spike (S) protein. This interaction is similar to the mechanism in SARS-CoV, a close relative of SARS-CoV-2, which was identified in 2003. Drugs and antibodies that inhibit the interaction between ACE2 and S proteins could be key therapeutic methods for preventing viral infection and replication in COVID-19. Here, we demonstrate the interaction between human ACE2 and a fragment of the S protein (S1 subunit) derived from SARS-CoV-2 and SARS-CoV using two-color fluorescence cross-correlation spectroscopy (FCCS), which can detect the interaction of fluorescently labeled proteins. The S1 subunit of SARS-CoV-2 interacted in solution with soluble ACE2, which lacks a transmembrane region, more strongly than that of SARS-CoV. Furthermore, one-to-one stoichiometry of the two proteins during the interaction was indicated. Thus, we propose that this FCCS-based interaction detection system can be used to analyze the interaction strengths of various mutants of the S1 subunit that have evolved during the worldwide pandemic, and also offers the opportunity to screen and evaluate the performance of drugs and antibodies that inhibit the interaction.
  • Akira Kitamura, Rika Numazawa, Masataka Kinjo
    Biochemical and Biophysical Research Communications 559 203 - 209 2021年06月 [査読有り][通常論文]
  • Akira Kitamura
    Methods in Molecular Biology 385 - 389 2021年05月 [査読無し][招待有り]
  • Akira Kitamura, Ai Fujimoto, Masataka Kinjo
    Journal of Visualized Experiments 170 e62576  2021年04月25日 [査読有り][招待有り]
     
    Protein aggregation is a hallmark of neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS), Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease (HD), and so on. To detect and analyze soluble or diffuse protein oligomers or aggregates, fluorescence correlation spectroscopy (FCS), which can detect the diffusion speed and brightness of a single particle with a single molecule sensitivity, has been used. However, the proper procedure and know-how for protein aggregation detection have not been widely shared. Here, we show a standard procedure of FCS measurement for diffusion properties of aggregation-prone proteins in cell lysate and live cells: ALS-associated 25 kDa carboxyl-terminal fragment of TAR DNA/RNA-binding protein 43 kDa (TDP25) and superoxide dismutase 1 (SOD1). The representative results show that a part of aggregates of green fluorescent protein (GFP)-tagged TDP25 was slightly included in the soluble fraction of murine neuroblastoma Neuro2a cell lysate. Moreover, GFP-tagged SOD1 carrying ALS-associated mutation shows a slower diffusion in live cells. Accordingly, we here introduce the procedure to detect the protein aggregation via its diffusion property using FCS.
  • Guang Yang, Shota Hiruma, Akira Kitamura, Masataka Kinjo, Mithilesh Mishra, Ryota Uehara
    Experimental cell research 403 2 112600 - 112600 2021年04月20日 [査読有り]
     
    The mechanism that mediates the interaction between the contractile ring and the plasma membrane during cytokinesis remains elusive. We previously found that ERM (Ezrin/Radixin/Moesin) proteins, which usually mediate cellular pole contraction, become over-accumulated at the cell equator and support furrow ingression upon the loss of other actin-membrane associated proteins, anillin and supervillin. In this study, we addressed the molecular basis of the exchangeability between ezrin and other actin-membrane associated proteins in mediating cortical contraction during cytokinesis. We found that depletion of anillin and supervillin caused over-accumulation of the membrane-associated FERM domain and actin-binding C-terminal domain (C-term) of ezrin at the cleavage furrow, respectively. This finding suggests that ezrin differentially shares its binding sites with these proteins on the actin cytoskeleton or inner membrane surface. Using chimeric mutants, we found that ezrin C-term, but not the FERM domain, can substitute for the corresponding anillin domains in cytokinesis and cell proliferation. On the other hand, either the membrane-associated or the actin/myosin-binding domains of anillin could not substitute for the corresponding ezrin domains in controlling cortical blebbing at the cell poles. Our results highlight specific designs of actin- or membrane-associated moieties of different actin-membrane associated proteins with limited exchangeability, which enables them to support diverse cortical activities on the shared actin-membrane interface during cytokinesis.
  • Hideo Takakura, Yuto Goto, Akira Kitamura, Toshitada Yoshihara, Seiji Tobita, Masataka Kinjo, Mikako Ogawa
    Journal of Photochemistry and Photobiology A: Chemistry 408 113094 - 113094 2021年03月 [査読有り][通常論文]
     
    © 2020 Elsevier B.V. Herein, we evaluated the intersystem crossing quantum yield (ΦISC) of a silicon phthalocyanine derivatized from IRDye700DX (IR700) which is used as a photosensitizer for photoimmunotherapy (PIT), using fluorescence correlation spectroscopy (FCS). The calculated ΦISC was 0.019 ± 0.002. The FCS measurement was validated by experiment in the presence of potassium iodide, which can change the kinetics of the relaxation process in the excited state.
  • Kanae Harusawa, Chiho Watanabe, Yuta Kobori, Kazuho Tomita, Akira Kitamura, Masataka Kinjo, Miho Yanagisawa
    Langmuir 37 1 437 - 444 2021年01月12日 [査読有り][通常論文]
  • Akira Kitamura, Masakata Kinjo
    BIO-PROTOCOL 10 10 2020年 [査読有り][招待有り]
  • Munechika Sugihara, Daisuke Morito, Shiori Ainuki, Yoshinobu Hirano, Kazutoyo Ogino, Akira Kitamura, Hiromi Hirata, Kazuhiro Nagata
    The Journal of cell biology 218 3 949 - 960 2019年03月04日 [査読有り][通常論文]
     
    Mysterin, also known as RNF213, is an intracellular protein that forms large toroidal oligomers. Mysterin was originally identified in genetic studies of moyamoya disease (MMD), a rare cerebrovascular disorder of unknown etiology. While mysterin is known to exert ubiquitin ligase and putative mechanical ATPase activities with a RING finger domain and two adjacent AAA+ modules, its biological role is poorly understood. Here, we report that mysterin is targeted to lipid droplets (LDs), ubiquitous organelles specialized for neutral lipid storage, and markedly increases their abundance in cells. This effect was exerted primarily through specific elimination of adipose triglyceride lipase (ATGL) from LDs. The ubiquitin ligase and ATPase activities of mysterin were both important for its proper LD targeting. Notably, MMD-related mutations in the ubiquitin ligase domain of mysterin significantly impaired its fat-stabilizing activity. Our findings identify a unique new regulator of cytoplasmic LDs and suggest a potential link between the pathogenesis of MMD and fat metabolism.
  • Tsubasa Hashimoto, Yuxin Ye, Asuka Matsuno, Yuki Ohnishi, Akira Kitamura, Masataka Kinjo, SatoshiAbe, Takafumi Ueno, MinYao, Tomohisa Ogawa, Takashi Matsui, Yoshikazu Tanaka
    Biochemical and Biophysical Research Communications 509 2 577 - 584 2019年02月 [査読有り][通常論文]
     
    Encapsulation of guest molecules into the hollow spaces of crystals has been applied for a variety of purposes such as structure determination, separation, and catalysis of the guest. Although host-guest studies have been developed mainly in crystals of small molecules, those of biomacromolecules have recently been applied. In those reports, a huge hollow space in the protein crystal is commonly used for encapsulation of the guest. Our previous study revealed that cylindrical hemocyanins stack inside the crystal as a linear hollow structure. The diameter of the linear hollow is approximately 110 Å, which is large enough for most proteins to pass through. In the present study, we evaluated the potential of hemocyanin crystals as a host to encapsulate biomacromolecules. Confocal microscopy revealed that hemocyanin crystals encapsulate proteins of molecular mass up to 250 kDa, i.e., 27 kDa green fluorescence protein, 105 kDa allophycocyanin, 220 kDa C-phycocyanin, and 250 kDa phycoerythrin, and DNAs up to 200-bp long, whereas 440 kDa ferritin not. Further analysis revealed that hemocyanin crystals prefer a negatively charged guest rather than a positive charge to encapsulate. Moreover, a photobleaching experiment showed that the guest does not move once entrapped. This knowledge of the host-guest study using the hollow hemocyanin crystal should be of significance for further application of hollow proteinaceous crystals as a host.
  • Takahashi S, Yamamoto J, Kitamura A, Kinjo M, Sugimoto N
    Analytical chemistry 91 4 2586 - 2590 2019年02月 [査読有り][通常論文]
     
    Molecular crowding creates a unique environment in cells and imposes physical constraints such as the excluded volume effect, water activity, and dielectric constant that can affect the structure and function of biomolecules. It is therefore important to develop a method for quantifying the effects of molecular crowding in cells. In this study, we developed a Förster resonance energy transfer (FRET) probe based on a guanine-quadruplex (G4) DNA motif that shows distinct FRET signals in response to crowding conditions in the presence of salt and poly(ethylene glycol). FRET efficiencies varied in different solutions, reflecting the dependence of G4 stability and topology on salt concentration and water activity. In living cells, FRET signals in the nucleus were higher than those in the cytosol; the signals in membraneless nuclear compartments (i.e., nucleolus) were especially high, suggesting that a decrease in water activity is important for the crowding effect in the nucleus. Thus, the use of DNA sensors with variable structures can elucidate the local effects of molecular crowding in cells.
  • Akira Kitamura, Hiroki Shimizu, Masataka Kinjo
    The Journal of Biochemistry 2018年09月01日 [査読有り][通常論文]
  • Maoko Tsukamoto, Kyoko Chiba, Yuriko Sobu, Yuzuha Shiraki, Yuka Okumura, Saori Hata, Akira Kitamura, Tadashi Nakaya, Seiichi Uchida, Masataka Kinjo, Hidenori Taru, Toshiharu Suzuki
    FEBS Letters 592 16 2716 - 2724 2018年08月 [査読有り][通常論文]
     
    Amyloid β-protein precursor (APP) is transported mainly by kinesin-1 and at a higher velocity than other kinesin-1 cargos, such as Alcadein α (Alcα); this is denoted by the enhanced fast velocity (EFV). Interaction of the APP cytoplasmic region with kinesin-1, which is essential for EFV transport, is mediated by JNK-interacting protein 1 (JIP1). To determine the roles of interactions between the APP luminal region and cargo components, we monitored transport of chimeric cargo receptors, Alcα (luminal)-APP (cytoplasmic) and APP (luminal)-Alcα (cytoplasmic). Alcα-APP is transported at the EFV, whereas APP-Alcα is transported at the same velocity as wild-type Alcα. Thus, the cytoplasmic region of APP is necessary and sufficient for the EFV of APP transport by kinesin-1.
  • Akira Kitamura, Ai Shibasaki, Kayo Takeda, Ryoji Suno, Masataka Kinjo
    Biochemistry and biophysics reports 14 58 - 63 2018年07月 [査読有り][通常論文]
     
    Normal function and abnormal aggregation of transactivation response (TAR) DNA/RNA-binding protein 43 kDa (TDP-43) are directly associated with the lethal genetic diseases: cystic fibrosis, amyotrophic lateral sclerosis (ALS), and frontotemporal lobar degeneration (FTLD). The binding of TDP-43 to single-stranded DNA (ssDNA) or RNA is involved in transcriptional repression, regulation of RNA splicing, and RNA stabilization. Equilibrium dissociation constants (Kd) of TDP-43 and ssDNA or RNA have been determined using various methods; however, methods that can measure Kd with high sensitivity in a short time using a small amount of TDP-43 in solution would be advantageous. Here, in order to determine the Kd of TDP-43 and fluorescence-labeled ssDNA as well as the binding stoichiometry, we use fluorescence correlation spectroscopy (FCS), which detects the slowed diffusion of molecular interactions in solution with single-molecule sensitivity, in addition to electrophoretic mobility shift assay (EMSA). Using tandem affinity chromatography of TDP-43 dually tagged with glutathione-S-transferase and poly-histidine tags, highly purified protein was obtained. FCS successfully detected specific interaction between purified TDP-43 and TG ssDNA repeats, with a Kd in the nanomolar range. The Kd of the TDP-43 mutant was not different from the wild type, although mutant oligomers, which did not bind ssDNA, were observed. Analysis of the fluorescence brightness per dimerized TDP-43/ssDNA complex was used to evaluate their binding stoichiometry. The results suggest that an assay combining FCS and EMSA can precisely analyze ssDNA recognition mechanisms, and that FCS may be applied for the rapid and quantitative determination of the interaction strength between TDP-43 and ssDNA or RNA. These methods will aid in the elucidation of the substrate recognition mechanism of ALS- and FTLD-associated variants of TDP-43.
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  • Akira Kitamura, Masataka Kinjo
    International Journal of Molecular Sciences 19 4 964  2018年04月01日 [査読有り][招待有り]
     
    Neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), Alzheimer’s disease, Parkinson’s disease, and Huntington’s disease, are devastating proteinopathies with misfolded protein aggregates accumulating in neuronal cells. Inclusion bodies of protein aggregates are frequently observed in the neuronal cells of patients. Investigation of the underlying causes of neurodegeneration requires the establishment and selection of appropriate methodologies for detailed investigation of the state and conformation of protein aggregates. In the current review, we present an overview of the principles and application of several methodologies used for the elucidation of protein aggregation, specifically ones based on determination of fluctuations of fluorescence. The discussed methods include fluorescence correlation spectroscopy (FCS), imaging FCS, image correlation spectroscopy (ICS), photobleaching ICS (pbICS), number and brightness (N& B) analysis, super-resolution optical fluctuation imaging (SOFI), and transient state (TRAST) monitoring spectroscopy. Some of these methodologies are classical protein aggregation analyses, while others are not yet widely used. Collectively, the methods presented here should help the future development of research not only into protein aggregation but also neurodegenerative diseases.
  • Akira Kitamura, Yoshihito Ishida, Hiroshi Kubota, Chan-Gi Pack, Takayuki Homma, Shinya Ito, Kazutaka Araki, Masataka Kinjo, Kazuhiro Nagata
    Biochemical and Biophysical Research Communications 497 1 279 - 284 2018年02月26日 [査読有り][通常論文]
     
    Heat shock protein 47 kDa (HSP47), an ER-resident and collagen-specific molecular chaperone, recognizes collagenous hydrophobic amino acid sequences (Gly-Pro-Hyp) and assists in secretion of correctly folded collagen. Elevated collagen production is correlated with HSP47 expression in various diseases, including fibrosis and keloid. HSP47 knockdown ameliorates liver fibrosis by inhibiting collagen secretion, and inhibition of the interaction of HSP47 with procollagen also prevents collagen secretion. Therefore, a high-throughput system for screening of drugs capable of inhibiting the interaction between HSP47 and collagen would aid the development of novel therapies for fibrotic diseases. In this study, we established a straightforward method for rapidly and quantitatively measuring the interaction between HSP47 and collagen in solution using fluorescence correlation spectroscopy (FCS). The diffusion rate of HSP47 labeled with Alexa Fluor 488 (HSP47-AF), a green fluorescent dye, decreased upon addition of type I or III collagen, whereas that of dye-labeled protein disulfide isomerase (PDI) or bovine serum albumin (BSA) did not, indicating that specific binding of HSP47 to collagen could be detected using FCS. Using this method, we calculated the dissociation constant of the interaction between HSP47 and collagen. The binding ratio between HSP47-AF and collagen did not change in the presence of sodium chloride, confirming that the interaction was hydrophobic in nature. In addition, we observed dissociation of collagen from HSP47 at low pH and re-association after recovery to neutral pH. These observations indicate that this system is appropriate for detecting the interaction between HSP47 and collagen, and could be applied to high-throughput screening for drugs capable of suppressing and/or curing fibrosis.
  • Ryuichi Ishida, Tomoya Okamoto, Fumihiro Motojima, Hiroshi Kubota, Hiroki Takahashi, Masako Tanabe, Toshihiko Oka, Akira Kitamura, Masataka Kinjo, Masasuke Yoshida, Michiro Otaka, Ewa Grave, Hideaki Itoh
    International Journal of Molecular Sciences 19 2 489  2018年02月06日 [査読有り][通常論文]
     
    The E. coli GroEL/GroES chaperonin complex acts as a folding cage by producing a bullet-like asymmetric complex, and GroEL exists as double rings regardless of the presence of adenosine triphosphate (ATP). Its mammalian chaperonin homolog, heat shock protein, HSP60, and co-chaperonin, HSP10, play an essential role in protein folding by capturing unfolded proteins in the HSP60/HSP10 complex. However, the structural transition in ATPase-dependent reaction cycle has remained unclear. We found nucleotide-dependent association and dissociation of the HSP60/HSP10 complex using various analytical techniques under near physiological conditions. Our results showed that HSP60 exist as a significant number of double-ring complexes (football-and bullet-type complexes) and a small number of single-ring complexes in the presence of ATP and HSP10. HSP10 binds to HSP60 in the presence of ATP, which increased the HSP60 double-ring formation. After ATP is hydrolyzed to Adenosine diphosphate (ADP), HSP60 released the HSP10 and the dissociation of the double-ring to single-rings occurred. These results indicated that HSP60/HSP10 undergoes an ATP-dependent transition between the single- and double-rings in their system that is highly distinctive from the GroEL/GroES system particularly in the manner of complex formation and the roles of ATP binding and hydrolysis in the reaction cycle.
  • Akira Kitamura
    Future Neurology 13 3 2018年 [査読有り][招待有り]
  • Akira Kitamura, Nodoka Iwasaki, Masataka Kinjo
    Cell Stress and Chaperones 2018年 [査読有り][通常論文]
  • Akira Kitamura, Masataka Kinjo
    Biophysics and Physicobiology 15 1 - 7 2018年 [査読有り][通常論文]
  • Masao Yahara, Akira Kitamura, Masataka Kinjo
    PLOS ONE 12 11 e0187813  2017年11月 [査読有り][通常論文]
     
    Depletion of amyotrophic lateral sclerosis (ALS)-associated transactivation response (TAR) RNA/DNA-binding protein 43 kDa (TDP-43) alters splicing efficiency of multiple transcripts and results in neuronal cell death. TDP-43 depletion can also disturb expression levels of small nuclear RNAs (snRNAs) as spliceosomal components. Despite this knowledge, the relationship between cell death and alteration of snRNA expression during TDP-43 depletion remains unclear. Here, we knocked down TDP-43 in murine neuroblastoma Neuro2A cells and found a time lag between efficient TDP-43 depletion and appearance of cell death, suggesting that several mechanisms mediate between these two events. The amount of U6 snRNA was significantly decreased during TDP-43 depletion prior to increase of cell death, whereas that of U1, U2, and U4 snRNAs was not. Downregulation of U6 snRNA led to cell death, whereas transient exogenous expression of U6 snRNA counteracted the effect of TDP-43 knockdown on cell death, and slightly decreased the mis-splicing rate of Dnajc5 and Sortilin 1 transcripts, which are assisted by TDP-43. These results suggest that regulation of the U6 snRNA expression level by TDP-43 is a key factor in the increase in cell death upon TDP-43 loss-of-function.
  • Akira Kitamura, Sachiko Yuno, Hideki Muto, Masataka Kinjo
    GENES TO CELLS 22 6 521 - 534 2017年06月 [査読有り][通常論文]
     
    The mechanism and cause of motor neuronal cell death in amyotrophic lateral sclerosis (ALS), a devastating neurodegenerative disorder, are unknown; gain of function of oligomers and aggregation of misfolded proteins, including carboxyl-terminal fragments (CTFs) of TAR RNA/DNA-binding protein 43 kDa (TDP-43), have been proposed as important causative factors in the onset of ALS. We recently reported that a nuclear localization signal (NLS)-tagged 25-kDa CTF of TDP-43 (TDP25) could decrease the cell-death proportion compared with that promoted by TDP25. Here, we show oligomeric states of NLS-TDP25 and its detailed localization property using super-resolution fluorescence microscopy, FRET, fluorescence recovery after photobleaching, and fluorescence correlation spectroscopy analysis. NLS-TDP25 efficiently formed a nucleolar cap structure via RNA binding in the presence of actinomycin D, but TDP25 did not. Although cytoplasmic inclusion bodies including TDP25 had a disordered and immobile structure, NLS-TDP25 in the nucleolus was ordered and dynamic. In the diffuse state, TDP25 formed fewer oligomers and interacted with the molecular chaperone, HSP70; however, NLS-TDP25 formed oligomers. These results suggested that NLS-tagged TDP25 can change its structure to use ordered oligomeric but nontoxic state. Moreover, the structure of ordered oligomers as well as nuclear sequestration may be important in mediating cytotoxicity in ALS pathology.
  • Tomoyo Ochiishi, Motomichi Doi, Kazuhiko Yamasaki, Keiko Hirose, Akira Kitamura, Takao Urabe, Nobutaka Hattori, Masataka Kinjo, Tatsuhiko Ebihara, Hideki Shimura
    SCIENTIFIC REPORTS 6 22712  2016年03月 [査読有り][通常論文]
     
    The intracellular accumulation of amyloid-beta (A beta) oligomers critically contributes to disease progression in Alzheimer's disease (AD) and can be the potential target of AD therapy. Direct observation of molecular dynamics of A beta oligomers in vivo is key for drug discovery research, however, it has been challenging because A beta aggregation inhibits the fluorescence from fusion proteins. Here, we developed A beta(1-42)-GFP fusion proteins that are oligomerized and visualize their dynamics inside cells even when aggregated. We examined the aggregation states of A beta-GFP fusion proteins using several methods and confirmed that they did not assemble into fibrils, but instead formed oligomers in vitro and in live cells. By arranging the length of the liker between A beta and GFP, we generated two fusion proteins with "a long-linker" and "a short-linker", and revealed that the aggregation property of fusion proteins can be evaluated by measuring fluorescence intensities using rat primary culture neurons transfected with A beta-GFP plasmids and A beta-GFP transgenic C. elegans. We found that A beta-GFP fusion proteins induced cell death in COS7 cells. These results suggested that novel A beta-GFP fusion proteins could be utilized for studying the physiological functions of A beta oligomers in living cells and animals, and for drug screening by analyzing A beta toxicity.
  • Takamitsu J. Morikawa, Hideaki Fujita, Akira Kitamura, Takashi Horio, Johtaro Yamamoto, Masataka Kinjo, Akira Sasaki, Hiroaki Machiyama, Keiko Yoshizawa, Taro Ichimura, Katsumi Imada, Takeharu Nagai, Tomonobu M. Watanabe
    SCIENTIFIC REPORTS 6 22342  2016年03月 [査読有り][通常論文]
     
    Fluorescent proteins have been widely used in biology because of their compatibility and varied applications in living specimens. Fluorescent proteins are often undesirably sensitive to intracellular conditions such as pH and ion concentration, generating considerable issues at times. However, harnessing these intrinsic sensitivities can help develop functional probes. In this study, we found that the fluorescence of yellow fluorescent protein (YFP) depends on the protein concentration in the solution and that this dependence can be enhanced by adding a glycine residue in to the YFP; we applied this finding to construct an intracellular protein-crowding sensor. A Frster resonance energy transfer (FRET) pair, involving a cyan fluorescent protein (CFP) insensitive to protein concentration and a glycine-inserted YFP, works as a genetically encoded probe to evaluate intracellular crowding. By measuring the fluorescence of the present FRET probe, we were able to detect dynamic changes in protein crowding in living cells.
  • Motosuke Tsutsumi, Hideki Muto, Shohei Myoba, Mai Kimoto, Akira Kitamura, Masakatsu Kamiya, Takashi Kikukawa, Shigeharu Takiya, Makoto Demura, Keiichi Kawano, Masataka Kinjo, Tomoyasu Aizawa
    FEBS OPEN BIO 6 2 106 - 125 2016年02月 [査読有り][通常論文]
     
    Fibroin modulator-binding protein 1 (FMBP-1) is a silkworm transcription factor that has a unique DNA-binding domain called the one score and three amino acid peptide repeat (STPR). Here we used fluorescence correlation spectroscopy (FCS) to analyze the diffusion properties of an enhanced green fluorescent protein-tagged FMBP-1 protein (EGFP-FMBP-1) expressed in posterior silk gland (PSG) cells of Bombyx mori at the same developmental stage as natural FMBP-1 expression. EGFP-FMBP-1 clearly localized to cell nuclei. From the FCS analyses, we identified an immobile DNA-bound component and three discernible diffusion components. We also used FCS to observe the movements of wild-type and mutant EGFP-FMBP-1 proteins in HeLa cells, a simpler experimental system. Based on previous in vitro observation, we also introduced a single amino acid substitution in order to suppress stable FMBP-1-DNA binding; specifically, we replaced the ninth Arg in the third repeat within the STPR domain with Ala. This mutation completely disrupted the slowest diffusion component as well as the immobile component. The diffusion properties of other FMBP-1 mutants (e.g. mutants with N-terminal or C-terminal truncations) were also analyzed. Based on our observations, we suggest that the four identifiable movements might correspond to four distinct FMBP-1 states: (a) diffusion of free protein, (b) and (c) two types of transient interactions between FMBP-1 and chromosomal DNA, and (d) stable binding of FMBP-1 to chromosomal DNA.
  • Akira Kitamura, Yusaku Nakayama, Ai Shibasaki, Ayami Taki, Sachiko Yuno, Kayo Takeda, Masao Yahara, Naoki Tanabe, Masataka Kinjo
    SCIENTIFIC REPORTS 6 19230  2016年01月 [査読有り][通常論文]
     
    A hallmark of amyotrophic lateral sclerosis (ALS), a devastating neurodegenerative disease, is formation of inclusion bodies (IBs) from misfolded proteins in neuronal cells. TAR RNA/DNA-binding protein 43 kDa (TDP43) is an ALS-causative protein forming IBs in ALS patients. The relation between localization of the IBs and neurotoxicity remains largely unknown. We characterized aggregation of fluorescently tagged TDP43 and its carboxyl-terminal fragments (CTFs) by analytical fluorescence imaging techniques. Quantitative time-lapse analysis in individual live cells showed that fluorescent-protein-tagged TDP43 was cleaved and a 35 kDa TDP43 CTF (TDP35) formed ubiquitin (Ub)-negative cytoplasmic IBs. Although TDP35 formed mildly toxic Ub-negative IBs in the cytoplasm, TDP25, another type of a TDP43 CTF, efficiently formed sufficiently toxic Ub-positive IBs. One-or two-color fluorescence correlation spectroscopy (FCS/FCCS) revealed that coaggregation of TDP25 with TDP43 was initiated by depletion of the RNA that binds to TDP25. Moreover, nuclear localization tagging TDP25 reduced the rate of neuronal cell death. These observations point to the need to elucidate the novel sequestration mechanism and details of the toxicity of the misfolded and aggregation-prone TDP43 CTFs (as well as the RNA binding and nuclear retention) in order to identify possible preventive interventions against ALS.
  • Akira Kitamura, Yusaku Nakayama, Masataka Kinjo
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 463 3 401 - 406 2015年07月 [査読有り][通常論文]
     
    Classical nuclear localization signal (NLS) sequences have been used for artificial localization of green fluorescent protein (GFP) in the nucleus as a positioning marker or for measurement of the nuclear-cytoplasmic shuttling rate in living cells. However, the detailed mechanism of nuclear retention of GFP-NLS remains unclear. Here, we show that a candidate mechanism for the strong nuclear retention of GFP-NLS is via the RNA-binding ability of the NLS sequence. GFP tagged with a classical NLS derived from Simian virus 40 (GFP-NLSSV40) localized not only in the nucleoplasm, but also to the nucleolus, the nuclear subdomain in which ribosome biogenesis takes place. GFP-NLSSV40 in the nucleolus was mobile, and intriguingly, the diffusion coefficient, which indicates the speed of diffusing molecules, was 1.5-fold slower than in the nucleoplasm. Fluorescence correlation spectroscopy (FCS) analysis showed that GFP-NLSSV40 formed oligomers via RNA binding, the estimated molecular weight of which was larger than the limit for passive nuclear export into the cytoplasm. These findings suggest that the nuclear localization of GFP-NLSSV40 likely results from oligomerization mediated via RNA binding. The analytical technique used here can be applied for elucidating the details of other nuclear localization mechanisms, including those of several types of nuclear proteins. In addition, GFP-NLSSV40 can be used as an excellent marker for studying both the nucleoplasm and nucleolus in living cells. (C) 2015 Elsevier Inc. All rights reserved.
  • Akira Kitamura, Kazuhiro Nagata, Masataka Kinjo
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 16 3 6076 - 6092 2015年03月 [査読有り][招待有り]
     
    Cellular homeostasis is maintained by several types of protein machinery, including molecular chaperones and proteolysis systems. Dysregulation of the proteome disrupts homeostasis in cells, tissues, and the organism as a whole, and has been hypothesized to cause neurodegenerative disorders, including amyotrophic lateral sclerosis (ALS) and Huntington's disease (HD). A hallmark of neurodegenerative disorders is formation of ubiquitin-positive inclusion bodies in neurons, suggesting that the aggregation process of misfolded proteins changes during disease progression. Hence, high-throughput determination of soluble oligomers during the aggregation process, as well as the conformation of sequestered proteins in inclusion bodies, is essential for elucidation of physiological regulation mechanism and drug discovery in this field. To elucidate the interaction, accumulation, and conformation of aggregation-prone proteins, in situ spectroscopic imaging techniques, such as Forster/fluorescence resonance energy transfer (FRET), fluorescence correlation spectroscopy (FCS), and bimolecular fluorescence complementation (BiFC) have been employed. Here, we summarize recent reports in which these techniques were applied to the analysis of aggregation-prone proteins (in particular their dimerization, interactions, and conformational changes), and describe several fluorescent indicators used for real-time observation of physiological states related to proteostasis.
  • 北村 朗
    バイオイメージング 23 1 12 - 17 2014年06月 [査読有り][招待有り]
  • Daisuke Morito, Kouki Nishikawa, Jun Hoseki, Akira Kitamura, Yuri Kotani, Kazumi Kiso, Masataka Kinjo, Yoshinori Fujiyoshi, Kazuhiro Nagata
    SCIENTIFIC REPORTS 4 4442  2014年03月 [査読有り][通常論文]
     
    Moyamoya disease is an idiopathic human cerebrovascular disorder that is characterized by progressive stenosis and abnormal collateral vessels. We recently identified mysterin/RNF213 as its first susceptibility gene, which encodes a 591-kDa protein containing enzymatically active P-loop ATPase and ubiquitin ligase domains and is involved in proper vascular development in zebrafish. Here we demonstrate that mysterin further contains two tandem AAA+ ATPase modules and forms huge ring-shaped oligomeric complex. AAA+ ATPases are known to generally mediate various biophysical and mechanical processes with the characteristic ring-shaped structure. Fluorescence correlation spectroscopy and biochemical evaluation suggested that mysterin dynamically changes its oligomeric forms through ATP/ADP binding and hydrolysis cycles. Thus, the moyamoya disease-associated gene product is a unique protein that functions as ubiquitin ligase and AAA+ ATPase, which possibly contributes to vascular development through mechanical processes in the cell.
  • Akira Kitamura, Noriko Inada, Hiroshi Kubota, Gen Matsumoto, Masataka Kinjo, Richard I. Morimoto, Kazuhiro Nagata
    GENES TO CELLS 19 3 209 - 224 2014年03月 [査読有り][通常論文]
     
    A hallmark of protein conformational disease, exemplified by neurodegenerative disorders, is the expression of misfolded and aggregated proteins. The relationship between protein aggregation and cellular toxicity is complex, and various models of experimental pathophysiology have often yielded conflicting or controversial results. In this study, we examined the biophysical properties of amyotrophic lateral sclerosis (ALS)-linked mutations of Cu/Zn superoxide dismutase 1 (SOD1) expressed in human tissue culture cells. Fluorescence correlation spectroscopy (FCS) and Forster resonance energy transfer (FRET) analyses revealed that changes in proteasome activity affected both the expression of FCS- and FRET-detected oligomers and cellular toxicity. Under normal conditions, highly aggregation-prone mutant SOD1 exhibited very little toxicity. However, when the activity of the proteasome was transiently inhibited, only upon recovery did we observe the appearance of ordered soluble oligomers, which were closely correlated with cellular toxicity. These results shed light on the importance of balance in proteostasis and suggest that transient shifts of activity in the cellular machinery can alter the course of protein conformational transitions and dysregulate modulation of proteasome activity. In neurodegenerative disorders including ALS, such changes may be a risk factor for pathogenesis.
  • Mariko Takano, Erika Tashiro, Akira Kitamura, Hiroshi Maita, Sanae M. M. Iguchi-Ariga, Masataka Kinjo, Hiroyoshi Ariga
    BRAIN RESEARCH 1542 186 - 194 2014年01月 [査読有り][通常論文]
     
    Protein aggregation is observed in various neurodegeneration diseases, including Parkinson's disease (PD). Alpha-synuclein, a causative gene product of familial PD, is a major component of large aggregates (inclusion bodies) in PD. Prefoldin, a molecular chaperone comprised of six subunits, PFD1 similar to 6, prevents misfolding of newly synthesized nascent polypeptides and also prevents aggregation of protein such as a' pathogenic form of Huntingtin, a causative gene product of Huntington disease. In this study, we first found that aggregation of TagRFP-tagged wild-type alpha-synuclein and its pathogenic mutants, but not that of GFP-tagged alpha-synuclein, occurred in transfected Neuro-2a cells. The fluorescence of GFP is weakened under the condition of pH 4.5-5.0, and TagRFP is a stable red fluorescence protein under an acidic condition. Aggregated TagRFP-wild-type alpha-synuclein and its pathogenic mutants in Neuro-2a cells were ubiquitinated and were colocalized with the prefoldin complex in the lysosome under this condition. Furthermore, knockdown of PFD2 and PFD5 disrupted prefoldin formation in alpha-synuclein-expressing cells, resulting in accumulation of aggregates of wild-type and pathogenic alpha-synuclein and in induction of cell death. The levels of aggregation and cell death in pathogenic alpha-synuclein-transfected cells tended to be higher than those in wild-type alpha-synuclein-transfected cells. These results suggest that prefoldin works as a protective factor in aggregated alpha-synucleininduced cell death. (C) 2013 Elsevier B.V. All rights reserved.
  • Shohei Ohta, Shigeko Kawai-Noma, Akira Kitamura, Chan-Gi Pack, Masataka Kinjo, Hideki Taguchi
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 442 1-2 28 - 32 2013年12月 [査読有り][通常論文]
     
    Prions are self-propagating amyloids. Yeast prion [PSI+] is a protein-based heritable element, in which amyloid aggregates of the Sup35 protein are transmitted to daughter cells. Hsp104, an ATP-dependent disaggregase, and other chaperones are essential to maintain [PSI+] Although previous reports have demonstrated the physical interactions of Hsp104 and Sup35 amyloids, the mechanism how Hsp104 interacts with Sup35 amyloids remains to be elucidated. Here we investigated the interaction between Hsp104 and Sup35 in the lysates of [PSI+] cells using fluorescence cross-correlation spectroscopy (FCCS), which can analyze the codiffusion events of different fluorophores. FCCS analysis showed a strong interaction between Hsp104 and Sup35 in [PSI+] lysates, but not in [psi(-)] lysates, suggesting that Hsp104 recognizes the amyloid aggregates of Sup35. Although the interaction was retained in ATP-depleted [PSI+] lysates, addition of ATP or guanidine hydrochloride, which is an inhibitor of Hspl 04, to [PSI+] lysates weakened the interaction. (C) 2013 Elsevier Inc. All rights reserved.
  • Erika Tashiro, Tamotsu Zako, Hideki Muto, Yoshinori Itoo, Karin Soergjerd, Naofumi Terada, Akira Abe, Makoto Miyazawa, Akira Kitamura, Hirotake Kitaura, Hiroshi Kubota, Mizuo Maeda, Takashi Momoi, Sanae M. M. Iguchi-Ariga, Masataka Kinjo, Hiroyoshi Ariga
    JOURNAL OF BIOLOGICAL CHEMISTRY 288 27 19958 - 19972 2013年07月 [査読有り][通常論文]
     
    Huntington disease is caused by cell death after the expansion of polyglutamine (polyQ) tracts longer than similar to 40 repeats encoded by exon 1 of the huntingtin (HTT) gene. Prefoldin is a molecular chaperone composed of six subunits, PFD1-6, and prevents misfolding of newly synthesized nascent polypeptides. In this study, we found that knockdown of PFD2 and PFD5 disrupted prefoldin formation in HTT-expressing cells, resulting in accumulation of aggregates of a pathogenic form of HTT and in induction of cell death. Dead cells, however, did not contain inclusions of HTT, and analysis by a fluorescence correlation spectroscopy indicated that knockdown of PFD2 and PFD5 also increased the size of soluble oligomers of pathogenic HTT in cells. In vitro single molecule observation demonstrated that prefoldin suppressed HTT aggregation at the small oligomer (dimer to tetramer) stage. These results indicate that prefoldin inhibits elongation of large oligomers of pathogenic Htt, thereby inhibiting subsequent inclusion formation, and suggest that soluble oligomers of polyQ-expanded HTT are more toxic than are inclusion to cells.
  • Takayuki Kiboku, Tsuyoshi Katoh, Akio Nakamura, Akira Kitamura, Masataka Kinjo, Yota Murakami, Masayuki Takahashi
    GENES TO CELLS 18 2 90 - 109 2013年02月 [査読有り][通常論文]
     
    Nonmuscle myosin II forms a folded conformation (10S form) in the inactivated state; however, the physiological importance of the 10S form is still unclear. To investigate the role of 10S form, we generated a chimeric mutant of nonmuscle myosin IIB (IIB-SK1 center dot 2), in which S1462-R1490 and L1551-E1577 were replaced with the corresponding portions of skeletal muscle myosin heavy chain. The IIB-SK1 center dot 2 mutant did not fold into a 10S form under physiological condition in vitro. IIB-SK1 center dot 2 was less dynamic by stabilizing the filamentous form and accumulated in the posterior region of migrating cells. IIB-SK1 center dot 2 functioned properly in cytokinesis but altered migratory properties; the rate and directional persistence were increased by IIB-SK1 center dot 2 expression. Surprisingly, endogenous nonmuscle myosin IIA was excluded from the posterior region of migrating cells expressing IIB-SK1 center dot 2, which may underlie the change of the cellular migratory properties. These results suggest that the 10S form is necessary for maintaining nonmuscle myosin II in an unassembled state and for recruitment of nonmuscle myosin II to a specific region of the cell.
  • Oikawa D, Kitamura A, Kinjo M, Iwawaki T
    PloS one 7 12 e51290  12 2012年12月 [査読有り][通常論文]
     
    IRE1, an ER-localized transmembrane protein, plays a central role in the unfolded protein response (UPR). IRE1 senses the accumulation of unfolded proteins in its luminal domain and transmits a signal to the cytosolic side through its kinase and RNase domains. Although the downstream pathways mediated by two mammalian IRE1s, IRE1 alpha and IRE1 beta, are well documented, their luminal events have not been fully elucidated. In particular, there have been no reports on how IRE1 beta senses the unfolded proteins. In this study, we performed a comparative analysis to clarify the luminal event mediated by the mammalian IRE1s. Confocal fluorescent microscopy using GFP-fused IRE1s revealed that IRE1 beta clustered into discrete foci upon ER stress. Also, fluorescence correlation spectroscopy (FCS) analysis in living cells indicated that the size of the IRE1 beta complex is robustly increased upon ER stress. Moreover, unlike IRE1 alpha, the luminal domain of IRE1 beta showed antiaggregation activity in vitro, and IRE1 beta was coprecipitated with the model unfolded proteins in cells. Strikingly, association with BiP was drastically reduced in IRE1 beta, while IRE1 alpha was associated with BiP and dissociated upon ER stress. This is the first report indicating that, differently from IRE1 alpha, the luminal event mediated by IRE1 beta involves direct interaction with unfolded proteins rather than association/dissociation with BiP, implying an intrinsic diversity in the sensing mechanism of mammalian sensors.
  • Hayashi Yamamoto, Soichiro Kakuta, Tomonobu M. Watanabe, Akira Kitamura, Takayuki Sekito, Chika Kondo-Kakuta, Rie Ichikawa, Masataka Kinjo, Yoshinori Ohsumi
    JOURNAL OF CELL BIOLOGY 198 2 219 - 233 2012年07月 [査読有り][通常論文]
     
    During the process of autophagy, cytoplasmic materials are sequestered by double-membrane structures, the autophagosomes, and then transported to a lytic compartment to be degraded. One of the most fundamental questions about autophagy involves the origin of the autophagosomal membranes. In this study, we focus on the intracellular dynamics of Atg9, a multispanning membrane protein essential for autophagosome formation in yeast. We found that the vast majority of Atg9 existed on cytoplasmic mobile vesicles (designated Atg9 vesicles) that were derived from the Golgi apparatus in a process involving Atg23 and Atg27. We also found that only a few Atg9 vesicles were required for a single round of autophagosome formation. During starvation, several Atg9 vesicles assembled individually into the preautophagosomal structure, and eventually, they are incorporated into the autophagosomal outer membrane. Our findings provide conclusive linkage between the cytoplasmic Atg9 vesicles and autophagosomal membranes and offer new insight into the requirement for Atg9 vesicles at the early step of autophagosome formation.
  • Hiroshi Kubota, Akira Kitamura, Kazuhiro Nagata
    METHODS 53 3 267 - 274 2011年03月 [査読有り][通常論文]
     
    Polyglutamine (polyQ)-expansion proteins cause protein aggregation in the cytosol and nucleus of neuronal cells, leading to neurodegenerative diseases. For example, expansion of the polyQ tract (>40 repeats) in huntingtin (htt) proteins leads to Huntington disease, while polyQ-expanded ataxins cause several types of ataxias. PolyQ-rich inclusions are found in neuronal cells of patients, suggesting that polyQ disease is caused by protein misfolding. However, the mechanisms by which polyQ-expansion proteins exert neuronal toxicity are largely unknown. Here, we review experimental procedures to analyze the roles of molecular chaperones in preventing polyQ aggregation and toxicity as well as to measure the characteristics and dynamics of polyQ aggregation, particularly focusing on cellular models and dynamic imaging of fluorescently-labeled polyQ-expansion proteins and their modulation by chaperones. (C) 2010 Elsevier Inc. All rights reserved.
  • Akira Kitamura, Hiroshi Kubota
    FEBS JOURNAL 277 6 1369 - 1379 2010年03月 [査読有り][通常論文]
     
    The accumulation of misfolded proteins in the cytosol and nucleus of neuronal cells leads to neurodegenerative disorders. Polyglutamine diseases are caused by polyglutamine-expanded proteins, whereas mutations in superoxide dismutase 1 lead to amyotrophic lateral sclerosis. These structurally unstable mutant species perturb essential interactions between normal proteins and tend to aggregate because of the presence of exposed hydrophobic surfaces. Accumulating evidence suggests that soluble species, including misfolded monomers and oligomers, are more toxic than large insoluble aggregates or inclusions. Spectroscopic analysis, including fluorescence recovery after photobleaching and fluorescence loss in photobleaching, in living cells revealed that protein aggregates of misfolded proteins are dynamic structures that interact with other proteins, such as molecular chaperones. Fluorescence correlation spectroscopy analysis detected soluble oligomers/aggregates of misfolded proteins in cell extracts. Fluorescence resonance energy transfer analysis supported the notion that soluble oligomers/aggregates are formed before the formation of inclusions in vivo. Here, we reviewed the characteristics of oligomers and aggregates of misfolded proteins, with a particular focus on those revealed by spectroscopic analysis, and discussed how these oligomers may be toxic to cells.
  • Tashiro Erika, Muto Hideki, Zako Tamotsu, Miyazawa Makoto, Kitaura Hirotake, Kitamura Akira, Kubota Hiroshi, Maeda Mizuo, Kinjo Masataka, Ariga Hiroyoshi
    NEUROSCIENCE RESEARCH 68 E310  2010年 [査読有り][通常論文]
  • Yoshihito Ishida, Akitsugu Yamamoto, Akira Kitamura, Shireen R. Lamande, Tamotsu Yoshimori, John F. Bateman, Hiroshi Kubota, Kazuhiro Nagata
    MOLECULAR BIOLOGY OF THE CELL 20 11 2744 - 2754 2009年06月 [査読有り][通常論文]
     
    Type I collagen is a major component of the extracellular matrix, and mutations in the collagen gene cause several matrix-associated diseases. These mutant procollagens are misfolded and often aggregated in the endoplasmic reticulum (ER). Although the misfolded procollagens are potentially toxic to the cell, little is known about how they are eliminated from the ER. Here, we show that procollagen that can initially trimerize but then aggregates in the ER are eliminated by an autophagy-lysosome pathway, but not by the ER-associated degradation (ERAD) pathway. Inhibition of autophagy by specific inhibitors or RNAi-mediated knockdown of an autophagy-related gene significantly stimulated accumulation of aggregated procollagen trimers in the ER, and activation of autophagy with rapamycin resulted in reduced amount of aggregates. In contrast, a mutant procollagen which has a compromised ability to form trimers was degraded by ERAD. Moreover, we found that autophagy plays an essential role in protecting cells against the toxicity of the ERAD-inefficient procollagen aggregates. The autophagic elimination of aggregated procollagen occurs independently of the ERAD system. These results indicate that autophagy is a final cell protection strategy deployed against ER-accumulated cytotoxic aggregates that are not able to be removed by ERAD.
  • Shoshiro Hirayama, Yuji Yamazaki, Akira Kitamura, Yukako Oda, Daisuke Morito, Katsuya Okawa, Hiroshi Kimura, Douglas M. Cyr, Hiroshi Kubota, Kazuhiro Nagata
    MOLECULAR BIOLOGY OF THE CELL 19 3 899 - 911 2008年03月 [査読有り][通常論文]
     
    McKusick-Kaufman syndrome (MKKS) is a recessively inherited human genetic disease characterized by several developmental anomalies. Mutations in the MKKS gene also cause Bardet-Biedl syndrome (BBS), a genetically heterogeneous disorder with pleiotropic symptoms. However, little is known about how MKKS mutations lead to disease. Here, we show that disease-causing mutants of MKKS are rapidly degraded via the ubiquitin-proteasome pathway in a manner dependent on HSC70 interacting protein (CHIP), a chaperone-dependent ubiquitin ligase. Although wild-type MKKS quickly shuttles between the centrosome and cytosol in living cells, the rapidly degraded mutants often fail to localize to the centrosome. Inhibition of proteasome functions causes MKKS mutants to form insoluble structures at the centrosome. CHIP and partner chaperones, including heat-shock protein (HSP) 70/heat-shock cognate 70 and HSP90, strongly recognize MKKS mutants. Modest knockdown of CHIP by RNA interference moderately inhibited the degradation of MKKS mutants. These results indicate that the MKKS mutants have an abnormal conformation and that chaperone-dependent degradation mediated by CHIP is a key feature of MKKS/BBS diseases.
  • Akira Kitamura, Hiroshi Kubota, Chan-Gi Pack, Gen Matsumoto, Shoshiro Hirayama, Yasuo Takahashi, Hiroshi Kimura, Masataka Kinjo, Richard I. Morimoto, Kazuhiro Nagata
    Nature Cell Biology 8 10 1163 - U224 2006年10月 [査読無し][通常論文]
     
    Polyglutamine (polyQ)-expansion proteins cause neurodegenerative disorders including Huntington's disease, Kennedy's disease and various ataxias. The cytotoxicity of these proteins is associated with the formation of aggregates or other conformationally toxic species. Here, we show that the cytosolic chaperonin CCT (also known as TRiC) can alter the course of aggregation and cytotoxicity of huntingtin (Htt) - polyQ proteins in mammalian cells. Disruption of the CCT complex by RNA-imediated knockdown enhanced Htt - polyQ aggregate formation and cellular toxicity. Analysis of the aggregation states of the Htt - polyQ proteins by fluorescence correlation spectroscopy revealed that CCT depletion results in the appearance of soluble Htt - polyQ aggregates. Similarly, overexpression of all eight subunits of CCT suppressed Htt aggregation and neuronal cell death. These results indicate that CCT has an essential role in protecting against the cytotoxicity of polyQ proteins by affecting the course of aggregation.
  • Y Ishida, H Kubota, A Yamamoto, A Kitamura, HP Bachinger, K Nagata
    MOLECULAR BIOLOGY OF THE CELL 17 5 2346 - 2355 2006年05月 [査読有り][通常論文]
     
    Heat-shock protein of 47 kDa (Hsp47) is a molecular chaperone that recognizes collagen triple helices in the endoplasmic reticulum (ER). Hsp47-knockout mouse embryos are deficient in the maturation of collagen types I and IV, and collagen triple helices formed in the absence of Hsp47 show increased susceptibility to protease digestion. We show here that the fibrils of type I collagen produced by Hsp47(-/-) cells are abnormally thin and frequently branched. Type I collagen was highly accumulated in the ER of Hsp47(-/-) cells, and its secretion rate was much slower than that of Hsp47(+/+) cells, leading to accumulation of the insoluble aggregate of type I collagen within the cells. Transient expression of Hsp47 in the Hsp47(-/-) cells restored normal extracellular fibril formation and intracellular localization of type I collagen. Intriguingly, type I collagen with unprocessed N-terminal propeptide (N-propeptide) was secreted from Hsp47(-/-) cells and accumulated in the extracellular matrix. These results indicate that Hsp47 is required for correct folding and prevention of aggregation of type I collagen in the ER and that this function is indispensable for efficient secretion, processing, and fibril formation of collagen.

MISC

書籍等出版物

  • 新・生細胞蛍光イメージング
    北村 朗 (担当:共著範囲:第21章，実習8-2)
    共立出版 2015年11月

講演・口頭発表等

  • 北村朗
    第46回 日本分子生物学会年会 2023年12月 シンポジウム・ワークショップパネル（指名）
  • Akira Kitamura
    第45回 日本分子生物学会年会 2022年11月 口頭発表（招待・特別）
  • Akira Kitamura
    第60回 日本生物物理学会年会 2022年09月 公開講演，セミナー，チュートリアル，講習，講義等
  • Akira Kitamura
    第60回 日本生物物理学会年会 2022年09月 口頭発表（招待・特別）
  • Akira Kitamura
    International Workshop on Fluorescence Methods and Applications 2022 2022年09月 口頭発表（招待・特別）
  • N末側の特性がTDP-43カルボキシル末端断片の凝集形成状態を決定する  [通常講演]
    北村朗, 呂依丹, 藤本愛, 川島怜維, 森谷香南, 高橋一帆, 金城正孝
    第72回 日本細胞生物学会年会 2021年07月 ポスター発表
  • The domain role for condensation of carboxyl-terminal fragments of TDP-43  [通常講演]
    Akira Kitamura
    FASEB SRC 2021 "The Protein Aggregation Conference: Function, Dysfunction, and Disease" ポスター発表
  • Aggregation process of carboxyl terminal fragments of TDP-43 protein  [通常講演]
    Akira Kitamura
    Cold Spring Harbor Laboratory 2020 Meeting "Protein homeostasis in Health & Disease" 2020年11月 ポスター発表
  • 北村朗
    サントリー生有研シンポジウム 2019年12月 公開講演，セミナー，チュートリアル，講習，講義等
  • Akira Kitamura
    QBP seminar, KTH Royal Institute of Technology 2019年11月 公開講演，セミナー，チュートリアル，講習，講義等
  • Akira Kitamura
    Asian Pacific Prion Symposium 2019 2019年10月 口頭発表（一般）
  • Akira Kitamura
    QBP-seminar, KTH Royal Institute of Technology 2018年11月 公開講演，セミナー，チュートリアル，講習，講義等
  • 蛍光ゆらぎを利用した生体分子構造変化の解析  [招待講演]
    北村 朗
    第55回 日本生化学会北海道支部例会，日本生物物理学会北海道支部合同シンポジウム 2018年07月 口頭発表（招待・特別）
  • Basics and application of fluorescence correlation spectroscopy  [招待講演]
    北村 朗
    5th AIST International Imaging Workshop 2018年01月 公開講演，セミナー，チュートリアル，講習，講義等
  • FCS and FCCS in living cells  [招待講演]
    北村 朗
    Course Functional Fluorescence Microscopy Imaging (fFMI) in Biomedical Research 2017年12月 公開講演，セミナー，チュートリアル，講習，講義等 Stockholm, Sweden
  • Basics and application of fluorescence correlation spectroscopy  [招待講演]
    北村 朗
    4th AIST International Imaging Workshop 2017年01月 口頭発表（招待・特別） 産業総合技術研究所
  • FRAP/FCSを用いた分子動態解析を用いた神経変性疾患原因研究の最前線  [招待講演]
    北村 朗
    第39回 日本分子生物学会年会 2016年12月 公開講演，セミナー，チュートリアル，講習，講義等
  • FCS and FCCS in living cells  [招待講演]
    北村 朗
    Course Functional Fluorescence Microscopy Imaging (fFMI) in Biomedical Research 2016年11月 口頭発表（招待・特別） カロリンスカ研究所，ストックホルム，スウェーデン
  • 蛍光イメージング手法を用いたALS関連TDP43凝集形成機構の解析  [招待講演]
    北村 朗
    第７回 ALSフォーラム 2016年07月 口頭発表（招待・特別） シェラトン都ホテル東京
  • Basics and application of fluorescence correlation spectroscopy  [招待講演]
    北村 朗
    3rd AIST International Imaging Workshop 2016年01月 口頭発表（招待・特別）
  • 蛍光相関分光法とFRETを用いた細胞内タンパク質品質管理機構の解析  [通常講演]
    北村 朗
    第55回日本植物生理学会年会 2014年03月 シンポジウム・ワークショップパネル（指名）
  • Yuno Sachiko, Kitamura Akira, Shibasaki Ai, Kinjo Masataka
    生物物理 2014年 一般社団法人 日本生物物理学会
  • 神経変性疾患に おける細胞内タンパク質恒常性  [招待講演]
    北村 朗
    「医と食の融合によるビジネス創出を目指して」 北大Ｒ＆ＢＰセミナー 2013年11月 公開講演，セミナー，チュートリアル，講習，講義等
  • 生細胞内FRET可視化法－フリーソフトウェアImageJを用いた画像演算実習－  [通常講演]
    北村 朗
    第五回「光塾」 2013年09月 公開講演，セミナー，チュートリアル，講習，講義等
  • 画像相関分光解析実習―点と点の相関性から何がわかるのか？―  [通常講演]
    佐々木章, 北村 朗
    第四回「光塾」 2012年08月 公開講演，セミナー，チュートリアル，講習，講義等
  • 生命科学画像解析における数学の基礎  [通常講演]
    北村 朗
    第三回「光塾」 2011年10月 公開講演，セミナー，チュートリアル，講習，講義等
  • 細胞内分子運動の解析－基礎から応用まで熱風のアシスト－  [通常講演]
    北村 朗
    第二回「光塾」 2010年12月 公開講演，セミナー，チュートリアル，講習，講義等
  • Erika Tashiro, Hideki Muto, Tamotsu Zako, Makoto Miyazawa, Hirotake Kitaura, Akira Kitamura, Hiroshi Kubota, Mizuo Maeda, Masataka Kinjo, Hiroyoshi Ariga
    NEUROSCIENCE RESEARCH 2010年 ELSEVIER IRELAND LTD
  • 画像解析プラティカ －ImageJ tipsからフリーウェアを用いた数値解析処理まで－  [通常講演]
    北村 朗
    第一回「光塾」 2009年08月 公開講演，セミナー，チュートリアル，講習，講義等
  • Kitamura Akira, Inada Noriko, Matsumoto Gen, Morimoto Richard I., Kubota Hiroshi, Nagata Kazuhiro, Kinjo Masataka
    生物物理 2008年 一般社団法人 日本生物物理学会
  • Kitamura Akira, Kubota Hiroshi, Pack Chan-Gi, Matsumoto Gen, Hirayama Shoshiro, Takahashi Yasuo, Kumura Hiroshi, Kinjo Masataka, Morimoto Richard I., Nagata Kazuhiro
    生物物理 2006年 一般社団法人 日本生物物理学会

担当経験のある科目（授業）

  • 細胞機能科学特論 （細胞分子機能科学）北海道大学大学院生命科学院
  • 細胞構造科学II北海道大学理学部生物科学科
  • 生命融合科学概論北海道大学大学院生命科学院
  • Life science special lecture III (Advanced Light Microscope in Life Science Research) as the Hokkaido Summer Institute北海道大学大学院生命科学院
  • Functional Fluorescence Microscopy Imaging (fFMI) in Biomedical ResearchKalorinska Institutet
  • 生体高分子実験（蛍光分光と生細胞蛍光イメージング実習）北海道大学理学部生物科学科
  • 高分子機能学基礎実験（光の回折と干渉）北海道大学理学部生物科学科
  • 脳科学研究の展開（先端脳機能イメージング）北海道大学脳科学教育研究センター
  • 生物系の反応速度論北海道大学理学部生物科学科
  • 実験生物科学（最先端蛍光イメージング手法）北海道大学理学部生物科学科
  • 細胞構造科学III北海道大学
  • AIST International Imaging WorkshopAssociation for Iron & Steel Technology, Japan
  • 細胞機能科学特論（細胞分子動態科学）北海道大学
  • 生物物理学秋田大学工学資源学部
  • 生命融合科学概論北海道大学大学院生命科学院

所属学協会

  • 日本細胞生物学会   日本生物物理学会   日本分子生物学会   日本RNA学会   

共同研究・競争的資金等の研究課題

  • 日本学術振興会：科学研究費助成事業
    研究期間 : 2024年04月 -2029年03月 
    代表者 : 北村 朗
  • AMED：「革新的先端研究開発支援事業ソロタイプ（AMED-PRIME）」 研究開発領域「プロテオスタシスの理解と革新的医療の創出」
    研究期間 : 2022年10月 -2026年03月 
    代表者 : 北村朗
  • 日本学術振興会：科学研究費助成事業
    研究期間 : 2022年04月 -2025年03月 
    代表者 : 金城 政孝, 北村 朗
  • 公益財団法人「篷庵社」：研究助成
    研究期間 : 2021年04月 -2025年03月
  • 日本学術振興会：科学研究費助成事業
    研究期間 : 2022年06月 -2024年03月 
    代表者 : 金城 政孝, 北村 朗
     
    細胞内の液-液相分離による分子集合体やタンパク質凝縮体、また細胞外に放出される細胞外小胞など、様々な形態や大きさを有する新規の構造体が細胞情報伝達や疾患など生体の重要な機能に関連することが認識されている。本研究では、そのような多彩な構造と幅広いサイズ分布を持つ分子集合体を一括して『細胞由来微粒子』として捉え、それらを対象とした散乱光による網羅的検出と蛍光による特異的検出を統合した新規定量的検出法の確立を目指している。 生体分子を対象とした蛍光と散乱光測定を融合した同時計測方法はこれまでになく、シグナル強度だけを見ると、散乱強度は極端に強く、蛍光は微弱であり、単純に比較することは困難である。申請者等は溶液中の分子や微粒子の特徴の一つである「揺れ動く」性質に着目した。蛍光・散乱測定に共通する時系列シグナル変化を基礎とする「自己相関解析」と、さらに蛍光と散乱光シグナル間の「相互相関解析」の同時利用で蛍光と散乱測定の二つの情報の統合と高度利用法を目指している。 具体的測定手段は申請者等が構築した不等分割光ファイバー型蛍光相関分光装置の散乱同時測定への展開と高度化である。本研究では特に細胞外微粒子の中でもガン診断の指標等として注目されている抗原提示エクソソームの定量的検出・同定法の確立を通してその性能を実証し、新規細胞由来微粒子検出法としての可能性を実証する 不当分割光ファイバーを利用した2色蛍光相互相関分光装置（FCrossCS）は、通常の励起光ダイクロイックミラー（第１次DM）を必要としないことから、これまで測定毎に必要とされた光軸・ピンホール調整等のキャリブレーションは一切不要となり、小型で長期安定な蛍光測定装置として利用でき、光軸調整不要なことから広い拡張性を有する。その拡張性の一つに、検出側の蛍光分光ダイクロイックミラー（２次）をハーフミラーに交換することで蛍光と散乱の同時測定を行なった。
  • AMED：「橋渡し研究プログラム異分野事業（シーズA）」
    研究期間 : 2023年04月 -2024年03月
  • AMED：「橋渡し研究プログラム異分野事業（シーズH）」
    研究期間 : 2022年09月 -2024年03月 
    代表者 : 北村朗
  • 日本学術振興会：科学研究費助成事業 新学術領域研究(研究領域提案型)
    研究期間 : 2022年04月 -2024年03月 
    代表者 : 北村 朗
  • 公益財団法人 萩原学術振興財団：2021年度 第2回研究助成
    研究期間 : 2022年04月 -2023年03月 
    代表者 : 北村朗
  • 公益財団法人 中谷医工計測技術振興財団：令和3年度 技術開発研究助成研究助成（開発研究助成）
    研究期間 : 2022年04月 -2023年03月 
    代表者 : 北村朗
  • 公益財団法人「中谷医工計測技術振興財団」：新型コロナウイルス感染症対策 助成プログラム
    研究期間 : 2020年07月 -2021年06月
  • JSPS：基盤研究C
    研究期間 : 2018年04月 -2021年03月 
    代表者 : 北村 朗
  • 光ファイバー型蛍光相関分光システムの研究開発と生物応用
    キヤノン財団：研究助成プログラム「産業基盤の創生」
    研究期間 : 2018年04月 -2020年03月 
    代表者 : 北村 朗
  • 日本学術振興会：科学研究費助成事業
    研究期間 : 2016年04月 -2019年03月 
    代表者 : 山本 条太郎, 北村 朗
     
    本研究ではブラウン運動するタンパク質分子のランダムな並進移動と回転の速さを解析する計測装置（偏光蛍光相関分光装置、Pol-FCS装置）を開発しました。この装置を用いることで、生きた細胞の中で細胞を生かしたまま分子のブラウン運動を計測し、分子の凝集の程度を推定できることを実証ました。さらに、同じ計測手法によって分子の向きがどれだけ揃っているか（配向性）や、溶液や細胞の中がどの程度分子で混み合っているのか（高分子混雑）を評価することも可能であることを発見し、Pol-FCSは研究開始当初想定した以上に有効な計測手法であることが分かりました。
  • 日本学術振興会：科学研究費助成事業
    研究期間 : 2017年 -2019年 
    代表者 : 北村 朗
     
    細胞内タンパク質恒常性の破綻に伴い形成されるミスフォールドタンパク質の蓄積は，細胞内においてしばしば凝集体を形成する．本研究では，筋萎縮性側索硬化症 (ALS)の原因タンパク質であるTDP25を発現する線虫株を樹立し，その運動能および寿命解析を行い，実際の個体に対して与える影響を明らかにした．また，凝集性タンパク質と結合するRNAについて，生細胞内における構造を読みだす新規蛍光分光手法の確立と構造を読み出す系を確立した．さらに，凝集形成に関与すると考えられる細胞内高分子クラウディングの状態をGFPの蛍光寿命を用いて読み出す方法も確立できた．
  • TDP43に潜在する非古典的核内輸送シグナル配列の同定と， 細胞質における神経細胞毒性低減機構の解明
    一般社団法人 日本ALS協会：ALS基金
    研究期間 : 2016年06月 -2017年03月 
    代表者 : 北村 朗
  • ALSのRNA治療に向けたTDP43のプリオン様構造転移および凝集形成を抑制するRNA分子の同定
    三井住友信託銀行公益信託：「生命の彩」ALS研究助成基金
    研究期間 : 2016年05月 -2017年03月 
    代表者 : 北村 朗
  • 日本学術振興会：学術研究助成基金助成金 基盤研究(Ｃ)
    研究期間 : 2014年04月 -2017年03月 
    代表者 : 北村 朗
     
    ポリペプチドが正しく折りたたまれないことにより生ずるミスフォールドタンパク質の蓄積は，細胞の生存にとってさまざまな悪影響を与え，筋萎縮性側索硬化症 (ALS)のような神経変性疾患の原因ともなり得る．本研究では，ALS原因タンパク質TDP43のカルボキシル末端断片であるTDP35またはTDP25の凝集構造の違いを，蛍光共鳴エネルギー移動 (FRET)法などを初めとする蛍光イメージング手法を用いて明らかにした．さらに，核局在化シグナルを付加したTDP25 (NLS-TDP25)が持つ秩序ある会合構造が封入体の性質を決め，細胞毒性を回避できることがわかった．
  • 細胞内化学反応解析のための超高速光計測システムの開発
    科学技術振興機構：先端計測分析技術・機器開発プログラム
    研究期間 : 2013年10月 -2017年03月 
    代表者 : 平岡 泰
  • 日本学術振興会：学術研究助成基金助成金 若手研究(Ｂ)
    研究期間 : 2011年04月 -2015年03月 
    代表者 : 北村 朗
     
    神経変性疾患の一種である筋萎縮性側索硬化症 (ALS)の責任遺伝子産物としてTDP43タンパク質が知られている．本研究では，TDP43タンパク質のカルボキシル末端側断片であるTDP25からRNAが解離することにより凝集し始めることを，蛍光相関分光法を用いることで明らかにした．次に，このTDP25が全長のTDP43タンパク質を巻き込むことで，細胞内で封入体を形成することを，共焦点レーザー顕微鏡観察により明らかにした．また，TDP25を発現させた神経細胞では，全長のTDP43を発現した時よりも，細胞死が高頻度で引き起こされることがわかった．
  • 文部科学省：科研費補助金 基盤研究(Ｓ)
    研究期間 : 2009年05月 -2014年03月 
    代表者 : 金城 政孝
     
    蛍光相関分光法（Fluorescence Correlation Spectroscopy，FCS）はダイナミックな分子間相互作用を単一分子レベルで解析する手法でるが、その一方で、励起光源にレーザー光が必要であり、その焦点領域である、特定の１点でしか測定出来ない。このことは生細胞が様々な区画に分かれていて、さらにその区画の中も不均一であるため、細胞生物学的応用の際の問題となっている。その解決のために本年も引き続き多点同時測定FCSの構築と生細胞測定への応用を目指ざしている。 そこでこれまで多点測定のためのまず、多点の焦点領域を作る必要がある。そのために空間光変調素子を利用したホログラフィ技術により複数照射の励起光パターンを作りだすことを可能とした。次に検出側としてマルチ光ファイバーと各端面に光電子増倍管を接続した多点検出装置を用いて，実際に生細胞内の多点におけるタンパク質の拡散運動を検出する装置を作成した。 次に本年は細胞応用測定に重点を置き、細胞質ならび細胞核を区別して7点同時測定を行った。 生細胞内GFPを対象としてガラス面からZ軸方向（上方向）に0.5ミクロンステップの空間分解能があることを証明し、次に細胞核膜を境にして同時7点測定FCS測定が可能であることを実証した。次に機能性タンパク質としてリガンド刺激により、細胞質から核へ移行するグルココルチコイドレセプター（GR）のGFP融合タンパク質を対象とした測定を行い、15秒おきのFCS多点同時測定に成功した。さらに本年は精度を上げるために細胞運動の抑制方法を種々検討し、ノコダゾール処理と、緩衝液を調整することで、長期の観測を可能とした。 安定測定が可能となったので、さらに時間分解を上げることが可能となったので、単一タンパク質分子の動態について、検出と解析を試みている。
  • 日本学術振興会：科学研究費助成事業
    研究期間 : 2011年 -2013年 
    代表者 : 久保田 広志, 永田 和宏, 金城 政孝, 北村 朗
     
    シャペロニンは、タンパク質のフォールディングを介助する分子シャペロンの１グループである。本研究では、ヒトをはじめとする真核細胞において重要な機能を担っているCCT（細胞質に分布）とHSP60（ミトコンドリアに分布）という２種のシャペロニンについて研究を行った。CCTについては、ATPase活性の他に、GTPase活性をもつことを見出した。HSP60に関しては、様々な解析の結果から、シングルリングから、ダブルリングを介して、フットボール型複合体へと変化し、フットボール型複合体が重要な機能を担っているものと考えられた。これらの結果は、シャペロニンの機能を知る上で重要な知見である
  • 文部科学省：科研費補助金 特定領域研究
    研究期間 : 2007年 -2011年 
    代表者 : 金城 政孝
     
    細胞の中ではその機能を支える分子が活発に動き回り,相互作用をしながらそれぞれの機能を支え,さらに細胞の高次機能を発現している。タンパク質の凝集体構造もある条件下では脱凝集を行うなど,細胞質内にある多くの分散しているタンパク質と交換していることが分かってきた。これまで細胞膜中でのタンパク質の動態を高感度に検出する全反射型蛍光相関分光法を開発してきた。これらの方法をさらに発展し同時多点測定可能なシステムの構築を行い,細胞膜や細胞内でのタンパク質の凝集や局在の変化をリアルタイムで検出する方法を開発することでタンパク質社会の解明を目的とした。
  • 日本学術振興会：科学研究費助成事業
    研究期間 : 2008年 -2010年 
    代表者 : 北村 朗
     
    神経変性疾患に共通してみられる現象として,神経細胞の機能低下とそれに続く細胞死がある.このような神経細胞死を引き起こす原因として,細胞内外に蓄積したタンパク質凝集体があげられる.筋萎縮性側索硬化症(Amyotrophic Lateral Screlosis ; ALS)では,原因遺伝子の約20%をSuperoxide dismutase 1(SOD1)が占めており,このSOD1タンパク質に変異が入ると凝集体を形成することが知られている.これらの変異タンパク質の凝集体が,細胞内のどのような場所でどのような構造にあるとき,細胞毒性を持つのか.そして細胞死に至るのかといった問題点を解明するため,細胞内の分解機構の一つであるプロテアソーム経路の阻害剤を用いたところ,変異型SOD1は細胞内で凝集体を形成した.さらに,プロテアソームの活性を回復させたところ,凝集体は脱凝集を介して消失した.これらの脱凝集過程は,プロテアソームの活性に大きく依存しており,細胞内における別の分解経路として知られているオートファジー・リソソーム経路は必須ではないことを見出した.また,蛍光相関分光法技術を用いることで,変異型SOD1タンパク質は生細胞のサイトゾルで複合体を形成していることが判明した.蛍光相関分光法の解析により,この複合体は変異型SOD1タンパク質のみを含むものではなく,他の細胞内因子が含まれていることが示唆された.さらに,免疫共沈降法・マススペクトル解析により,分子シャペロンHsc70などが含まれていることが明らかとなった.このことから,細胞内において凝集体の毒性を抑制する際に,分子シャペロンが関与していることが示唆された.
  • 日本学術振興会：科学研究費助成事業
    研究期間 : 2006年 -2007年 
    代表者 : 北村 朗
     
    本年度は,従来より研究を進めていたポリグルタミンタンパク質のように変異によって凝集体を形成し,神経細胞死を招くと考えられている変異型SOD1タンパク質の凝集体形成について主に解析を行った.SOD1タンパク質は,難病指定された神経変性疾患の一つである家族性筋萎縮性側索硬化症(fALS)の原因遺伝子である.最初に,プロテアソーム阻害剤であるMG-132処理により,変異型SOD1では,核近傍に,ユビキチン化されたタンパク質や分子シャペロンなどが集積したアグレソーム様の凝集体構造を形成していることを明らかにした.さらに,MG-132処理によって形成された凝集体構造は,プロテアソームの活性回復に伴い,消失することを見出した.この消失過程を詳細に解析した結果,一度形成された凝集体を解きほぐす脱凝集機構が関与していることが示唆された.また,凝集過程よりも脱凝集過程における細胞死の頻度が高いことから,脱凝集過程において発生する分子の構造もしくは多量体化状態が毒性を発揮する可能性があると考え,蛍光相関分光法による分子サイズの解析より,脱凝集過程において,可溶性のオリゴマーはすみやかに消失することから,毒性を発揮するのは,大きな多量体ではなく,低分子で構造の転移したものではないかという仮説提唱に至った.これらの結果は,昨年度公開した研究成果のようなポリグルタミンタンパク質で得られた知見とは異なり,SOD1の場合は,多量体化したオリゴマーが毒性を発揮するのではなく,低分子であっても毒性を発揮しうる状態があるのではないかと考えられる. 続いて,細胞質シャペロニンCCTと弱い相同性を持つタンパク質であるMKKSPについても解析を行った.MKKSPは中心体に豊富に局在していることが,これまでの解析から明らかにされていたが,今年度の研究では,MKKSPが中心体と細胞質の間をすみやかに移動しているが,少ない割合の成分は中心体に滞留し,何かしらの機能を発現していることが示唆された.

産業財産権

  • 特願PCT/JP2022/041001:ＴＤＰ４３、ＴＤＰ３５、またはＴＤＰ２５の凝集を特徴とする神経変性疾患の治療剤、進行抑制剤、および予防剤  2022年11月02日
    北村朗, 藤本愛  国立大学法人 北海道大学
  • 特開2017-214339:ヘモシアニン会合体を用いた包摂体の製造方法  2017年12月07日
    田中 良和, 松野 明日香, 北村 朗, 金城 政孝, 姚 閔, 上野 隆史, 安部 聡

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