Rate of force generation in muscle: correlation with actomyosin ATPase activity in solution.
- 1 May 1986
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 83 (10) , 3542-3546
- https://doi.org/10.1073/pnas.83.10.3542
Abstract
Crossbridge models of muscle contraction based on biochemical studies predict that there may be a relationship between the rate-limiting step in the actomyosin ATPase cycle in vitro and the rate of force development in vivo. In the present study, we measured the rate of force redevelopment in skinned rabbit muscle fibers following unloaded isotonic shortening and a rapid restretch. For comparison, ATPase activity was measured under identical conditions, using myosin subfragment-1 chemically crosslinked to actin. We found that the time course of force redevelopment is well fitted by a single exponential function, implying that force redevelopment is a first-order process, described by a single rate constant. The magnitude of this rate constant is in close agreement with the rate constant necessary to simulate the experimental force-velocity relation on the basis of a crossbridge model of the type proposed by A. F. Huxley in 1957. In addition, the observed close correlation between the rate constant for force redevelopment and the maximal actin-activated actomyosin ATPase rate under a variety of conditions suggests that the step that determines the rate of force generation in the crossbridge cycle may be the physiological equivalent of the rate-limiting step in the actomyosin ATPase cycle in solution.This publication has 21 references indexed in Scilit:
- ADP dissociation from actomyosin subfragment 1 is sufficiently slow to limit the unloaded shortening velocity in vertebrate muscle.Proceedings of the National Academy of Sciences, 1985
- Structure of the actin–myosin interfaceNature, 1981
- The Relation of Muscle Biochemistry to Muscle PhysiologyAnnual Review of Physiology, 1980
- Cross-bridge model of muscle contraction. Quantitative analysisBiophysical Journal, 1980
- Rate of isometric tension development in relation to calcium binding of skinned muscle fibresPflügers Archiv - European Journal of Physiology, 1979
- Mechanism of the actomyosin adenosine triphosphatase. Evidence that adenosine 5'-triphosphate hydrolysis can occur without dissociation of the actomyosin complexBiochemistry, 1979
- Tension responses to sudden length change in stimulated frog muscle fibres near slack lengthThe Journal of Physiology, 1977
- Kinetics of reaction in calcium-activated skinned muscle fibresNature, 1976
- Mechanism of Actomyosin ATPase and the Problem of Muscle ContractionPublished by Elsevier ,1973
- The Interaction of Actin with Myosin and Heavy Meromyosin in Solution at Low Ionic StrengthJournal of Biological Chemistry, 1967