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Myosin-binding protein C (MyBPC) is proposed to take on a trimeric collar arrangement around the thick filament backbone in cardiac muscle, based on interactions between cardiac MyBPC domains C5 and C8. We have now determined, using yeast two-hybrid and in vitro binding assays, that the C5:C8 interaction is not dependent on the 28-residue cardiac-specific insert in C5. Furthermore, an interaction of similar affinity occurs between domains C5 and C8 of fast skeletal muscle MyBPC, but not between these domains of the slow skeletal muscle protein. These data have implications for the role and quaternary structure of MyBPC in skeletal muscle.

Original publication

DOI

10.1016/j.febslet.2008.01.004

Type

Journal article

Journal

FEBS Lett

Publication Date

06/02/2008

Volume

582

Pages

434 - 438

Keywords

Amino Acid Sequence, Carrier Proteins, Dimerization, Humans, Models, Molecular, Molecular Sequence Data, Muscle Fibers, Fast-Twitch, Muscle Fibers, Slow-Twitch, Muscle, Skeletal, Mutant Proteins, Myocardium, Protein Binding, Protein Structure, Quaternary, Protein Structure, Tertiary, Sequence Homology, Amino Acid, Two-Hybrid System Techniques, Yeasts