Literature DB >> 33010234

The Location and Rate of the Phosphate Release Step in the Muscle Cross-Bridge Cycle.

Gerald Offer1, K W Ranatunga2.   

Abstract

It is controversial whether the phosphate (Pi) release step in the cross-bridge cycle occurs before or after the first tension-generating step and whether it is fast or slow. We have therefore modified our previous model of the frog cross-bridge cycle by including a Pi release step either before (model A) or after (model B) the first tension-generating step and refined the two models by downhill simplex runs against experimental data for the force-velocity relation and the tension transients after length steps. Pi release step was initially made slow (70 s-1), but after refinement, it became fast (∼500 s-1 for model A and ∼6000 s-1 for model B). The two models gave similar fits to the experimental tension transients after length steps, but model A gave a better fit to the lengthening limb of the force-velocity relation than model B. 50 mM Pi inhibited the isometric tension of model A by ∼50% but that of model B by only ∼25%. The half-inhibition was at 6.0 mM Pi for model A and at 1.6 mM Pi for model B. The values for model A were consistent with experimental data. We also simulated the effect Pi jump as in caged Pi experiments. For model A, a Pi jump induced a tension fall at a rate similar to the experimental phase II. There was then a small rise in tension to the steady state mimicking the experimental phase III. The initial tension fall was caused by detachment of M⋅ADP⋅Pi myosin heads from actin and reversal of the first tension-generating step. For model B, the fall in tension was more rapid and due to reversal of the first tension-generating step, and phase III was not observed. We conclude that, as in model A, the Pi release step is before the first tension-generating step and is moderately fast.
Copyright © 2020 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2020        PMID: 33010234      PMCID: PMC7642309          DOI: 10.1016/j.bpj.2020.09.004

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


  60 in total

1.  Effect of inorganic phosphate on the force and number of myosin cross-bridges during the isometric contraction of permeabilized muscle fibers from rabbit psoas.

Authors:  Marco Caremani; Jody Dantzig; Yale E Goldman; Vincenzo Lombardi; Marco Linari
Journal:  Biophys J       Date:  2008-10-03       Impact factor: 4.033

2.  Two step mechanism of phosphate release and the mechanism of force generation in chemically skinned fibers of rabbit psoas muscle.

Authors:  M Kawai; H R Halvorson
Journal:  Biophys J       Date:  1991-02       Impact factor: 4.033

3.  Depletion of phosphate in active muscle fibers probes actomyosin states within the powerstroke.

Authors:  E Pate; K Franks-Skiba; R Cooke
Journal:  Biophys J       Date:  1998-01       Impact factor: 4.033

4.  Force Responses and Sarcomere Dynamics of Cardiac Myofibrils Induced by Rapid Changes in [Pi].

Authors:  Robert Stehle
Journal:  Biophys J       Date:  2017-01-24       Impact factor: 4.033

5.  Mechanical properties of skinned rabbit psoas and soleus muscle fibres during lengthening: effects of phosphate and Ca2+.

Authors:  G J Stienen; P G Versteeg; Z Papp; G Elzinga
Journal:  J Physiol       Date:  1992       Impact factor: 5.182

6.  Tension responses to rapid pressure release in glycerinated rabbit muscle fibers.

Authors:  N S Fortune; M A Geeves; K W Ranatunga
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-15       Impact factor: 11.205

7.  A kinetic model that explains the effect of inorganic phosphate on the mechanics and energetics of isometric contraction of fast skeletal muscle.

Authors:  Marco Linari; Marco Caremani; Vincenzo Lombardi
Journal:  Proc Biol Sci       Date:  2009-10-07       Impact factor: 5.349

8.  An asymmetry in the phosphate dependence of tension transients induced by length perturbation in mammalian (rabbit psoas) muscle fibres.

Authors:  K W Ranatunga; Moira E Coupland; G Mutungi
Journal:  J Physiol       Date:  2002-08-01       Impact factor: 5.182

9.  Exchange between inorganic phosphate and adenosine 5'-triphosphate in the medium by actomyosin subfragment 1.

Authors:  J A Sleep; R L Hutton
Journal:  Biochemistry       Date:  1980-04-01       Impact factor: 3.162

10.  Suppression of muscle contraction by vanadate. Mechanical and ligand binding studies on glycerol-extracted rabbit fibers.

Authors:  J A Dantzig; Y E Goldman
Journal:  J Gen Physiol       Date:  1985-09       Impact factor: 4.086

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  1 in total

Review 1.  Recent insights into the relative timing of myosin's powerstroke and release of phosphate.

Authors:  Edward P Debold
Journal:  Cytoskeleton (Hoboken)       Date:  2022-03-21
  1 in total

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