The hypertrophic cardiomyopathy myosin mutation R453C alters ATP-binding and hydrolysis of human cardiac beta-myosin.

Journal article

Bloemink, M., Deacon, J., Langer, S., Vera, C., Combs, A., Leindwand, L. and Geeves, M. 2014. The hypertrophic cardiomyopathy myosin mutation R453C alters ATP-binding and hydrolysis of human cardiac beta-myosin. The Journal of Biological Chemistry. 289 (8), pp. 5158-5167. https://doi.org/10.1074/jbc.M113.511204
AuthorsBloemink, M., Deacon, J., Langer, S., Vera, C., Combs, A., Leindwand, L. and Geeves, M.
Abstract

The human hypertrophic cardiomyopathy mutation R453C results in one of the more severe forms of the myopathy. Arg-453 is found in a conserved surface loop of the upper 50-kDa domain of the myosin motor domain and lies between the nucleotide binding pocket and the actin binding site. It connects to the cardiomyopathy loop via a long α-helix, helix O, and to Switch-2 via the fifth strand of the central β-sheet. The mutation is, therefore, in a position to perturb a wide range of myosin molecular activities. We report here the first detailed biochemical kinetic analysis of the motor domain of the human β-cardiac myosin carrying the R453C mutation. A recent report of the same mutation (Sommese, R. F., Sung, J., Nag, S., Sutton, S., Deacon, J. C., Choe, E., Leinwand, L. A., Ruppel, K., and Spudich, J. A. (2013) Proc. Natl. Acad. Sci. U.S.A. 110, 12607–12612) found reduced ATPase and in vitro motility but increased force production using an optical trap. Surprisingly, our results show that the mutation alters few biochemical kinetic parameters significantly. The exceptions are the rate constants for ATP binding to the motor domain (reduced by 35%) and the ATP hydrolysis step/recovery stroke (slowed 3-fold), which could be the rate-limiting step for the ATPase cycle. Effects of the mutation on the recovery stroke are consistent with a perturbation of Switch-2 closure, which is required for the recovery stroke and the subsequent ATP hydrolysis.

KeywordsActin Cardiac Muscle Cardiomyopathy Fluorescence Kinetics Myosin Homology Models Protein Structure-Function Sequence Alignment
Year2014
JournalThe Journal of Biological Chemistry
Journal citation289 (8), pp. 5158-5167
PublisherAmerican Society for Biochemistry and Molecular Biology
ISSN0021-9258
Digital Object Identifier (DOI)https://doi.org/10.1074/jbc.M113.511204
FunderWellcome Trust
NIH
Publication dates
Print21 Feb 2014
Publication process dates
Deposited31 Oct 2014
Output statusPublished
References

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