Cryo-EM structure of the human cardiac myosin filament

Debabrata Dutta (), Vu Nguyen, Kenneth S. Campbell, Raúl Padrón () and Roger Craig ()
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Debabrata Dutta: University of Massachusetts Chan Medical School
Vu Nguyen: University of Massachusetts Chan Medical School
Kenneth S. Campbell: University of Kentucky
Raúl Padrón: University of Massachusetts Chan Medical School
Roger Craig: University of Massachusetts Chan Medical School

Nature, 2023, vol. 623, issue 7988, 853-862

Abstract: Abstract Pumping of the heart is powered by filaments of the motor protein myosin that pull on actin filaments to generate cardiac contraction. In addition to myosin, the filaments contain cardiac myosin-binding protein C (cMyBP-C), which modulates contractility in response to physiological stimuli, and titin, which functions as a scaffold for filament assembly1. Myosin, cMyBP-C and titin are all subject to mutation, which can lead to heart failure. Despite the central importance of cardiac myosin filaments to life, their molecular structure has remained a mystery for 60 years2. Here we solve the structure of the main (cMyBP-C-containing) region of the human cardiac filament using cryo-electron microscopy. The reconstruction reveals the architecture of titin and cMyBP-C and shows how myosin’s motor domains (heads) form three different types of motif (providing functional flexibility), which interact with each other and with titin and cMyBP-C to dictate filament architecture and function. The packing of myosin tails in the filament backbone is also resolved. The structure suggests how cMyBP-C helps to generate the cardiac super-relaxed state3; how titin and cMyBP-C may contribute to length-dependent activation4; and how mutations in myosin and cMyBP-C might disturb interactions, causing disease5,6. The reconstruction resolves past uncertainties and integrates previous data on cardiac muscle structure and function. It provides a new paradigm for interpreting structural, physiological and clinical observations, and for the design of potential therapeutic drugs.

Date: 2023
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DOI: 10.1038/s41586-023-06691-4

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