Functional differences between the N-terminal domains of mouse and human myosin binding protein-C.

J Biomed Biotechnol

Department of Neurobiology, Physiology and Behavior, University of California-Davis, Davis, CA 95616-8519, USA.

Published: September 2010

The N-terminus of cMyBP-C can activate actomyosin interactions in the absence of Ca2+, but it is unclear which domains are necessary. Prior studies suggested that the Pro-Ala rich region of human cMyBP-C activated force in permeabilized human cardiomyocytes, whereas the C1 and M-domains of mouse cMyBP-C activated force in permeabilized rat cardiac trabeculae. Because the amino acid sequence of the P/A region differs between human and mouse cMyBP-C isoforms (46% identity), we investigated whether species-specific differences in the P/A region could account for differences in activating effects. Using chimeric fusion proteins containing combinations of human and mouse C0, Pro-Ala, and C1 domains, we demonstrate here that the human P/A and C1 domains activate actomyosin interactions, whereas the same regions of mouse cMyBP-C are less effective. These results suggest that species-specific differences between homologous cMyBP-C isoforms confer differential effects that could fine-tune cMyBP-C function in hearts of different species.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2850553PMC
http://dx.doi.org/10.1155/2010/789798DOI Listing

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