Literature DB >> 2838100

Energetics of the actomyosin bond in the filament array of muscle fibers.

E Pate1, R Cooke.   

Abstract

The interaction between actin and myosin in the filament array of glycerinated muscle fibers has been monitored using paramagnetic probes and mechanical measurements. Both fiber stiffness and the spectra of probes bound to a reactive sulfydral on the myosin head were measured as the actomyosin bond was weakened by addition of magnesium pyrophosphate (MgPPi) and glycerol. In the absence of MgPPi, all myosin heads are attached to actin with oriented probes. When fibers were incubated in buffers containing MgPPi, a fraction of the probes became disordered, and this effect was greater in the presence of glycerol. To determine whether the heads with disordered probes were detached from actin, spin-labeled myosin subfragment-1 (MSL-S1) was diffused into unlabeled fibers, and the fractions bound to actin and free in the medium were correlated with the oriented and disordered spectral components. These experiments showed that the label was oriented when MSL-S1 was attached to actin in a ternary complex with the ligand and that all heads with disordered probes were detached from actin. Thus the fraction of oriented labels could be used to determine the fraction of heads attached to actin in a fiber in the presence of ligand. The fraction of myosin heads attached to actin decreased with increasing [MgPPi], and in the absence of glycerol approximately 50% of the myosin heads were dissociated at 3.3 mM ligand with little change in fiber stiffness. In the presence of 37% glycerol plus ligand, up to 80% of the heads could be detached with a 50% decrease in fiber stiffness. The data indicate that there are two populations of myosin heads in the fiber. All the data could be fit with a model in which one population of myosin heads (comprising approximately 50% of the total) sees an apparent actin concentration of 0.1 mM and can be released from actin with little change in fiber stiffness. A second population of myosin heads (approximately 50%) sees a higher actin concentration (5 mM) and is only released in the presence of both glycerol and ligand.

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Year:  1988        PMID: 2838100      PMCID: PMC1330230          DOI: 10.1016/S0006-3495(88)83136-9

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


  44 in total

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Authors:  D D Thomas; R Cooke
Journal:  Biophys J       Date:  1980-12       Impact factor: 4.033

7.  The relation between stiffness and filament overlap in stimulated frog muscle fibres.

Authors:  L E Ford; A F Huxley; R M Simmons
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8.  The effect of nucleotide on the binding of myosin subfragment 1 to regulated actin.

Authors:  L Greene
Journal:  J Biol Chem       Date:  1982-12-10       Impact factor: 5.157

9.  Orientation of spin-labeled nucleotides bound to myosin in glycerinated muscle fibers.

Authors:  M S Crowder; R Cooke
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  35 in total

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6.  Orientational disorder and motion of weakly attached cross-bridges.

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8.  Structural dynamics of the actomyosin complex probed by a bifunctional spin label that cross-links SH1 and SH2.

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9.  Altered cross-bridge characteristics following haemodynamic overload in rabbit hearts expressing V3 myosin.

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Journal:  J Physiol       Date:  2001-10-15       Impact factor: 5.182

10.  Orientation of spin-labeled light chain-2 exchanged onto myosin cross-bridges in glycerinated muscle fibers.

Authors:  B Hambly; K Franks; R Cooke
Journal:  Biophys J       Date:  1991-01       Impact factor: 4.033

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