Literature DB >> 8534819

Approximating the isometric force-calcium relation of intact frog muscle using skinned fibers.

D W Maughan1, J E Molloy, M A Brotto, R E Godt.   

Abstract

In previous papers we used estimates of the composition of frog muscle and calculations involving the likely fixed charge density in myofibrils to propose bathing solutions for skinned fibers, which best mimic the normal intracellular milieu of intact muscle fibers. We tested predictions of this calculation using measurements of the potential across the boundary of skinned frog muscle fibers bathed in this solution. The average potential was -3.1 mV, close to that predicted from a simple Donnan equilibrium. The contribution of ATP hydrolysis to a diffusion potential was probably small because addition of 1 mM vanadate to the solution decreased the fiber actomyosin ATPase rate (measured by high-performance liquid chromatography) by at least 73% but had little effect on the measured potential. Using these solutions, we obtained force-pCa curves from mechanically skinned fibers at three different temperatures, allowing the solution pH to change with temperature in the same fashion as the intracellular pH of intact fibers varies with temperature. The bath concentration of Ca2+ required for half-maximal activation of isometric force was 1.45 microM (22 degrees C, pH 7.18), 2.58 microM (16 degrees C, pH 7.25), and 3.36 microM (5 degrees C, pH 7.59). The [Ca2+] at the threshold of activation at 16 degrees C was approximately 1 microM, in good agreement with estimates of threshold [Ca2+] in intact frog muscle fibers.

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Year:  1995        PMID: 8534819      PMCID: PMC1236379          DOI: 10.1016/S0006-3495(95)80019-6

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


  38 in total

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  5 in total

1.  Protein osmotic pressure and the state of water in frog myoplasm.

Authors:  D W Maughan; R E Godt
Journal:  Biophys J       Date:  2001-01       Impact factor: 4.033

2.  Coupled expression of troponin T and troponin I isoforms in single skeletal muscle fibers correlates with contractility.

Authors:  Marco A Brotto; Brandon J Biesiadecki; Leticia S Brotto; Thomas M Nosek; Jian-Ping Jin
Journal:  Am J Physiol Cell Physiol       Date:  2005-09-28       Impact factor: 4.249

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Authors:  M Konishi; M Watanabe
Journal:  J Gen Physiol       Date:  1998-04       Impact factor: 4.086

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Authors:  S Hollingworth; M Zhao; S M Baylor
Journal:  J Gen Physiol       Date:  1996-11       Impact factor: 4.086

5.  Fluorescence changes on contractile activation in TnC(DANZ) labeled skinned rabbit psoas fibers.

Authors:  M Huang; D Burkhoff; F Schachat; P W Brandt
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  5 in total

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