Literature DB >> 2939452

Rate of force generation in muscle: correlation with actomyosin ATPase activity in solution.

B Brenner, E Eisenberg.   

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.

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Year:  1986        PMID: 2939452      PMCID: PMC323553          DOI: 10.1073/pnas.83.10.3542

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  21 in total

Review 1.  Mechanism of actomyosin ATPase and the problem of muscle contraction.

Authors:  E W Taylor
Journal:  CRC Crit Rev Biochem       Date:  1979

2.  Mechanism of actomyosin adenosine triphosphatase. Evidence that adenosine 5'-triphosphate hydrolysis can occur without dissociation of the actomyosin complex.

Authors:  L A Stein; R P Schwarz; P B Chock; E Eisenberg
Journal:  Biochemistry       Date:  1979-09-04       Impact factor: 3.162

3.  Kinetics of reaction in calcium-activated skinned muscle fibres.

Authors:  D G Moisescu
Journal:  Nature       Date:  1976-08-12       Impact factor: 49.962

4.  Tension responses to sudden length change in stimulated frog muscle fibres near slack length.

Authors:  L E Ford; A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

5.  The interaction of actin with myosin and heavy meromyosin in solution at low ionic strength.

Authors:  E Eisenberg; C Moos
Journal:  J Biol Chem       Date:  1967-06-25       Impact factor: 5.157

6.  Structure of the actin-myosin interface.

Authors:  D Mornet; R Bertrand; P Pantel; E Audemard; R Kassab
Journal:  Nature       Date:  1981-07-23       Impact factor: 49.962

7.  Rate of isometric tension development in relation to calcium binding of skinned muscle fibres.

Authors:  P J Griffiths; H J Kuhn; K Güth; J C Rüegg
Journal:  Pflugers Arch       Date:  1979-11       Impact factor: 3.657

8.  Cross-bridge model of muscle contraction. Quantitative analysis.

Authors:  E Eisenberg; T L Hill; Y Chen
Journal:  Biophys J       Date:  1980-02       Impact factor: 4.033

Review 9.  The relation of muscle biochemistry to muscle physiology.

Authors:  E Eisenberg; L E Greene
Journal:  Annu Rev Physiol       Date:  1980       Impact factor: 19.318

10.  ADP dissociation from actomyosin subfragment 1 is sufficiently slow to limit the unloaded shortening velocity in vertebrate muscle.

Authors:  R F Siemankowski; M O Wiseman; H D White
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

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  208 in total

1.  Effects of sarcomere length and temperature on the rate of ATP utilisation by rabbit psoas muscle fibres.

Authors:  K Hilber; Y B Sun; M Irving
Journal:  J Physiol       Date:  2001-03-15       Impact factor: 5.182

2.  Regulation of skeletal muscle tension redevelopment by troponin C constructs with different Ca2+ affinities.

Authors:  M Regnier; A J Rivera; P B Chase; L B Smillie; M M Sorenson
Journal:  Biophys J       Date:  1999-05       Impact factor: 4.033

3.  ATP consumption and efficiency of human single muscle fibers with different myosin isoform composition.

Authors:  Z H He; R Bottinelli; M A Pellegrino; M A Ferenczi; C Reggiani
Journal:  Biophys J       Date:  2000-08       Impact factor: 4.033

4.  Structural characterization of weakly attached cross-bridges in the A*M*ATP state in permeabilized rabbit psoas muscle.

Authors:  S Xu; J Gu; G Melvin; L C Yu
Journal:  Biophys J       Date:  2002-04       Impact factor: 4.033

5.  Mutation of the myosin converter domain alters cross-bridge elasticity.

Authors:  Jan Köhler; Gerhard Winkler; Imke Schulte; Tim Scholz; William McKenna; Bernhard Brenner; Theresia Kraft
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-19       Impact factor: 11.205

6.  Cross-bridge cooperativity during isometric contraction and unloaded shortening of skeletal muscle.

Authors:  V A Barnett
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

7.  pH modulation of the kinetics of a Ca2(+)-sensitive cross-bridge state transition in mammalian single skeletal muscle fibres.

Authors:  J M Metzger; R L Moss
Journal:  J Physiol       Date:  1990-09       Impact factor: 5.182

8.  Activation kinetics of skinned cardiac muscle by laser photolysis of nitrophenyl-EGTA.

Authors:  Hunter Martin; Marcus G Bell; Graham C R Ellis-Davies; Robert J Barsotti
Journal:  Biophys J       Date:  2004-02       Impact factor: 4.033

9.  Isotonic force modulates force redevelopment rate of intact frog muscle fibres: evidence for cross-bridge induced thin filament activation.

Authors:  Rene Vandenboom; James D Hannon; Gary C Sieck
Journal:  J Physiol       Date:  2002-09-01       Impact factor: 5.182

10.  Dependency of the force-velocity relationships on Mg ATP in different types of muscle fibers from Xenopus laevis.

Authors:  G J Stienen; W J van der Laarse; G Elzinga
Journal:  Biophys J       Date:  1988-06       Impact factor: 4.033

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