Literature DB >> 3790690

The effect of cross-bridge clustering and head-head competition on the mechanical response of skeletal muscle under equilibrium conditions.

A Tözeren, M Schoenberg.   

Abstract

The effect of cross-bridge clustering and head-head competition on the mechanical response of skeletal muscle under equilibrium conditions is considered. For this purpose, the recent multiple site equilibrium cross-bridge model of Schoenberg (Schoenberg, M., 1985, Biophys. J., 48:467-475) is extended in accordance with the formalism of T.L. Hill (1974, Prog. Biophys, Mol. Biol., 28:267-340) to consider the case where groups of independent cross-bridge heads compete with each other for binding to multiple actin sites. Cooperative behavior between heads is not allowed. Computations indicate that for the double-headed cross-bridge with two independent equivalent heads, the time course of force decay after a stretch is similar to that for the single-headed cross-bridge; that is, the rate constant for force decay is approximately equal to the cross-bridge head detachment rate constant. The results also show that the force decay after a stretch becomes slower than the detachment rate constant of a single head when cross-bridge heads bind adjacently in clusters so that competition between heads for binding to the available actin sites increases. However, if one assumes that the detachment rate constant of an unstrained head in a fiber is comparable to that of an S1 molecule in solution, this effect is not large enough to explain why some of the rate constants for force decay after a stretch in rigor, or in the presence of ATP analogues such as adenyl-5'-yl imidodiphosphate, appear to be significantly slower than the detachment rate constant of S1 from actin in solution.

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Year:  1986        PMID: 3790690      PMCID: PMC1329812          DOI: 10.1016/S0006-3495(86)83528-7

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  15 in total

1.  Muscle structure and theories of contraction.

Authors:  A F HUXLEY
Journal:  Prog Biophys Biophys Chem       Date:  1957

2.  Stiffness of skinned rabbit psoas fibers in MgATP and MgPPi solution.

Authors:  B Brenner; J M Chalovich; L E Greene; E Eisenberg; M Schoenberg
Journal:  Biophys J       Date:  1986-10       Impact factor: 4.033

3.  Mechanism of adenosine triphosphate hydrolysis by actomyosin.

Authors:  R W Lymn; E W Taylor
Journal:  Biochemistry       Date:  1971-12-07       Impact factor: 3.162

4.  Evidence for cross-bridge attachment in relaxed muscle at low ionic strength.

Authors:  B Brenner; M Schoenberg; J M Chalovich; L E Greene; E Eisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1982-12       Impact factor: 11.205

5.  Cross-bridge attachment in relaxed muscle.

Authors:  M Schoenberg; B Brenner; J M Chalovich; L E Greene; E Eisenberg
Journal:  Adv Exp Med Biol       Date:  1984       Impact factor: 2.622

6.  Equilibrium muscle cross-bridge behavior. Theoretical considerations.

Authors:  M Schoenberg
Journal:  Biophys J       Date:  1985-09       Impact factor: 4.033

7.  Muscle cross-bridge kinetics in rigor and in the presence of ATP analogues.

Authors:  M Schoenberg; E Eisenberg
Journal:  Biophys J       Date:  1985-12       Impact factor: 4.033

8.  Cross-bridge behavior in rigor muscle.

Authors:  E F Pate; C J Brokaw
Journal:  Biophys Struct Mech       Date:  1980

9.  Kinetic and thermodynamic properties of the ternary complex between F-actin, myosin subfragment 1 and adenosine 5'-[beta, gamma-imido]triphosphate.

Authors:  M Konrad; R S Goody
Journal:  Eur J Biochem       Date:  1982-11-15

10.  Transient kinetics of adenosine 5'-diphosphate and adenosine 5'-(beta, gamma-imidotriphosphate) binding to subfragment 1 and actosubfragment 1.

Authors:  K M Trybus; E W Taylor
Journal:  Biochemistry       Date:  1982-03-16       Impact factor: 3.162

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  10 in total

1.  Cell-cell conjugation. Transient analysis and experimental implications.

Authors:  A Tozeren
Journal:  Biophys J       Date:  1990-09       Impact factor: 4.033

2.  Effect of ionic strength on skinned rabbit psoas fibers in the presence of magnesium pyrophosphate.

Authors:  M Schoenberg
Journal:  Biophys J       Date:  1991-09       Impact factor: 4.033

3.  Equilibrium muscle cross-bridge behavior. Theoretical considerations. II. Model describing the behavior of strongly-binding cross-bridges when both heads of myosin bind to the actin filament.

Authors:  M Schoenberg
Journal:  Biophys J       Date:  1991-09       Impact factor: 4.033

4.  Simulation of stochastic processes in motile crossbridge systems.

Authors:  E Pate; R Cooke
Journal:  J Muscle Res Cell Motil       Date:  1991-08       Impact factor: 2.698

5.  Strain dependence of the elastic properties of force-producing cross-bridges in rigor skeletal muscle.

Authors:  U van der Heide; M Ketelaars; B W Treijtel; E L de Beer; T Blangé
Journal:  Biophys J       Date:  1997-02       Impact factor: 4.033

6.  Slip of rabbit striated muscle in rigor or AMPPNP.

Authors:  B Somasundaram; A Newport; R Tregear
Journal:  J Muscle Res Cell Motil       Date:  1989-10       Impact factor: 2.698

7.  Possible cooperativity in crossbridge detachment in muscle fibers having magnesium pyrophosphate at the active site.

Authors:  M L Anderson; M Schoenberg
Journal:  Biophys J       Date:  1987-12       Impact factor: 4.033

8.  The influence of doubly attached crossbridges on the mechanical behavior of skeletal muscle fibers under equilibrium conditions.

Authors:  A Tozeren
Journal:  Biophys J       Date:  1987-11       Impact factor: 4.033

9.  Effect of adenosine triphosphate analogues on skeletal muscle fibers in rigor.

Authors:  M Schoenberg
Journal:  Biophys J       Date:  1989-07       Impact factor: 4.033

10.  ADP binding to myosin cross-bridges and its effect on the cross-bridge detachment rate constants.

Authors:  M Schoenberg; E Eisenberg
Journal:  J Gen Physiol       Date:  1987-06       Impact factor: 4.086

  10 in total

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