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Compr Physiol. 2018 Mar 13;8(2):631-709. doi: 10.1002/cphy.c170023.

Thick Filament Protein Network, Functions, and Disease Association.

Author information

1
Department of Biochemistry and Molecular Biology, University of Maryland, Baltimore, Maryland, USA.

Abstract

Sarcomeres consist of highly ordered arrays of thick myosin and thin actin filaments along with accessory proteins. Thick filaments occupy the center of sarcomeres where they partially overlap with thin filaments. The sliding of thick filaments past thin filaments is a highly regulated process that occurs in an ATP-dependent manner driving muscle contraction. In addition to myosin that makes up the backbone of the thick filament, four other proteins which are intimately bound to the thick filament, myosin binding protein-C, titin, myomesin, and obscurin play important structural and regulatory roles. Consistent with this, mutations in the respective genes have been associated with idiopathic and congenital forms of skeletal and cardiac myopathies. In this review, we aim to summarize our current knowledge on the molecular structure, subcellular localization, interacting partners, function, modulation via posttranslational modifications, and disease involvement of these five major proteins that comprise the thick filament of striated muscle cells. © 2018 American Physiological Society. Compr Physiol 8:631-709, 2018.

PMID:
29687901
PMCID:
PMC6404781
DOI:
10.1002/cphy.c170023
[Indexed for MEDLINE]
Free PMC Article

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