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Cardiac muscle thin filament structures reveal calcium regulatory mechanism

Author

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  • Yurika Yamada

    (Osaka University)

  • Keiichi Namba

    (Osaka University
    RIKEN Center for Biosystems Dynamics Research and SPring-8 Center
    Osaka University)

  • Takashi Fujii

    (Osaka University
    Osaka University)

Abstract

Contraction of striated muscles is driven by cyclic interactions of myosin head projecting from the thick filament with actin filament and is regulated by Ca2+ released from sarcoplasmic reticulum. Muscle thin filament consists of actin, tropomyosin and troponin, and Ca2+ binding to troponin triggers conformational changes of troponin and tropomyosin to allow actin-myosin interactions. However, the structural changes involved in this regulatory mechanism remain unknown. Here we report the structures of human cardiac muscle thin filament in the absence and presence of Ca2+ by electron cryomicroscopy. Molecular models in the two states built based on available crystal structures reveal the structures of a C-terminal region of troponin I and an N-terminal region of troponin T in complex with the head-to-tail junction of tropomyosin together with the troponin core on actin filament. Structural changes of the thin filament upon Ca2+ binding now reveal the mechanism of Ca2+ regulation of muscle contraction.

Suggested Citation

  • Yurika Yamada & Keiichi Namba & Takashi Fujii, 2020. "Cardiac muscle thin filament structures reveal calcium regulatory mechanism," Nature Communications, Nature, vol. 11(1), pages 1-9, December.
    • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-019-14008-1
    DOI: 10.1038/s41467-019-14008-1
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