UMMS Affiliation

Department of Cell and Developmental Biology; Department of Radiology; Craig Lab

Publication Date

2-21-2017

Document Type

Article

Disciplines

Biochemistry | Cell Biology | Cellular and Molecular Physiology

Abstract

Cardiac myosin binding protein C (cMyBP-C) has a key regulatory role in cardiac contraction, but the mechanism by which changes in phosphorylation of cMyBP-C accelerate cross-bridge kinetics remains unknown. In this study, we isolated thick filaments from the hearts of mice in which the three serine residues (Ser273, Ser282, and Ser302) that are phosphorylated by protein kinase A in the m-domain of cMyBP-C were replaced by either alanine or aspartic acid, mimicking the fully nonphosphorylated and the fully phosphorylated state of cMyBP-C, respectively. We found that thick filaments from the cMyBP-C phospho-deficient hearts had highly ordered cross-bridge arrays, whereas the filaments from the cMyBP-C phospho-mimetic hearts showed a strong tendency toward disorder. Our results support the hypothesis that dephosphorylation of cMyBP-C promotes or stabilizes the relaxed/superrelaxed quasi-helical ordering of the myosin heads on the filament surface, whereas phosphorylation weakens this stabilization and binding of the heads to the backbone. Such structural changes would modulate the probability of myosin binding to actin and could help explain the acceleration of cross-bridge interactions with actin when cMyBP-C is phosphorylated because of, for example, activation of beta1-adrenergic receptors in myocardium.

Rights and Permissions

Freely available online through the PNAS open access option.

DOI of Published Version

10.1073/pnas.1614020114

Source

Proc Natl Acad Sci U S A. 2017 Feb 21;114(8):E1355-E1364. doi: 10.1073/pnas.1614020114. Epub 2017 Feb 6. Link to article on publisher's site

Related Resources

Link to Article in PubMed

Keywords

cMyBP-C, cardiac myosin binding protein C, cardiac myosin binding protein C function, cardiac thick filament, cardiac thick filament structure

Journal/Book/Conference Title

Proceedings of the National Academy of Sciences of the United States of America

PubMed ID

28167762

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