Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 118, Issue 13, Pages -Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.2024288118
Keywords
thin filament; cryoelectron microscopy; cardiac regulation; muscle contraction; troponin complex
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Funding
- NIH [R01 HL140925, U24 GM116790, U24 GM116788, S10-RR025067, R01 HL128683]
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The study reveals the structural composition of cardiac thin filaments under systolic Ca2+ levels, showing that the two strands of the thin filament consist of troponin complexes with different binding states and short-range cooperativity. These findings suggest a mechanism by which cardiac muscle is regulated by narrow range Ca2+ fluctuations.
Every heartbeat relies on cyclical interactions between myosin thick and actin thin filaments orchestrated by rising and falling Ca2+ levels. Thin filaments are comprised of two actin strands, each harboring equally separated troponin complexes, which bind Ca2+ to move tropomyosin cables away from the myosin binding sites and, thus, activate systolic contraction. Recently, structures of thin filaments obtained at low (pCa similar to 9) or high (pCa similar to 3) Ca2+ levels revealed the transition between the Ca2+-free and Ca2+-bound states. However, in working cardiac muscle, Ca2+ levels fluctuate at intermediate values between pCa similar to 6 and pCa similar to 7. The structure of the thin filament at physiological Ca2+ levels is unknown. We used cryoelectron microscopy and statistical analysis to reveal the structure of the cardiac thin filament at systolic pCa = 5.8. We show that the two strands of the thin filament consist of a mixture of regulatory units, which are composed of Ca2+-free, Ca2+-bound, or mixed (e.g., Ca2+ free on one side and Ca2+ bound on the other side) troponin complexes. We traced troponin complex conformations along and across individual thin filaments to directly determine the structural composition of the cardiac native thin filament at systolic Ca2+ levels. We demonstrate that the two thin filament strands are activated stochastically with short-range cooperativity evident only on one of the two strands. Our findings suggest a mechanism by which cardiac muscle is regulated by narrow range Ca2+ fluctuations.
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