Literature DB >> 1403812

Reversal of the cross-bridge force-generating transition by photogeneration of phosphate in rabbit psoas muscle fibres.

J A Dantzig1, Y E Goldman, N C Millar, J Lacktis, E Homsher.   

Abstract

1. Orthophosphate (P(i), 0.1-2.0 mM) was photogenerated within the filament lattice of isometrically contracting glycerinated fibres of rabbit psoas muscle at 10 and 20 degrees C. The P(i) was produced by laser flash photolysis of the photolabile compound 1-(2-nitrophenyl)ethylphosphate (caged P(i)). Caged P(i) caused a depression of tension that was much smaller than that caused by P(i). 2. Photolysis of caged P(i) produced a decline in isometric force composed of four phases: phase I, a lag phase (e.g. 1-4 ms at 10 degrees C) during which force did not change; phase II, an exponential decline by as much as 20% of the pre-pulse force; phase III, a partial force recovery (0-3% of the pre-pulse force); and phase IV, a further slow (0.5-3 s) decline to the steady value. Phases I, III and IV were largely independent of [P(i)] and are likely to be indirect effects caused by the caged P(i) photolysis. 3. Both the rate and amplitude of phase II depended markedly on [P(i)]. The amplitude of phase II was similar to the reduction of steady-state force by P(i). The rate of phase II increased with increasing temperature and [P(i)]. At high [P(i)] the rate began to saturate, and approached limits of 123 s-1 at 10 degrees C and 194 s-1 at 20 degrees C. 4. The rate of phase II was independent of sarcomere overlap, while the amplitude was proportional to tension at partial filament overlap. A control experiment using caged ATP showed that phase II was not produced by the photolytic by-products or the light pulse. The results suggest that phase II is associated with the force-generating transition of the cross-bridge cycle. 5. Sinusoidal length oscillations at 0.5 and 2 kHz were used to measure muscle stiffness during phase II. Stiffness declined in a single exponential phase, with the same time course as phase II of the tension transient. The change in stiffness was 83 +/- 6% (mean +/- S.E.M., n = 10, 0.5 kHz) of the change in tension when both signals were normalized to their pre-flash values. 6. Analysis of the data shows that two steps are involved in force generation and P(i) release. The non-force exerting AM-ADP-P(i) cross-bridge state first isomerizes to form a force-exerting cross-bridge state (AM'-ADP-P(i)). P(i) is then released to form a second force-generating state, AM'-ADP.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1992        PMID: 1403812      PMCID: PMC1176160          DOI: 10.1113/jphysiol.1992.sp019163

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  27 in total

1.  Energetics and mechanism of actomyosin adenosine triphosphatase.

Authors:  H D White; E W Taylor
Journal:  Biochemistry       Date:  1976-12-28       Impact factor: 3.162

Review 2.  Caged compounds and striated muscle contraction.

Authors:  E Homsher; N C Millar
Journal:  Annu Rev Physiol       Date:  1990       Impact factor: 19.318

3.  Addition of phosphate to active muscle fibers probes actomyosin states within the powerstroke.

Authors:  E Pate; R Cooke
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4.  Measurement of sarcomere shortening in skinned fibers from frog muscle by white light diffraction.

Authors:  Y E Goldman
Journal:  Biophys J       Date:  1987-07       Impact factor: 4.033

5.  Changes in the ATPase activity of insect fibrillar flight muscle during sinusoidal length oscillation probed by phosphate-water oxygen exchange.

Authors:  J Lund; M R Webb; D C White
Journal:  J Biol Chem       Date:  1988-04-25       Impact factor: 5.157

6.  Relaxation of rabbit psoas muscle fibres from rigor by photochemical generation of adenosine-5'-triphosphate.

Authors:  Y E Goldman; M G Hibberd; D R Trentham
Journal:  J Physiol       Date:  1984-09       Impact factor: 5.182

7.  Phosphate release and force generation in skeletal muscle fibers.

Authors:  M G Hibberd; J A Dantzig; D R Trentham; Y E Goldman
Journal:  Science       Date:  1985-06-14       Impact factor: 47.728

8.  Oxygen exchange between Pi in the medium and water during ATP hydrolysis mediated by skinned fibers from rabbit skeletal muscle. Evidence for Pi binding to a force-generating state.

Authors:  M R Webb; M G Hibberd; Y E Goldman; D R Trentham
Journal:  J Biol Chem       Date:  1986-11-25       Impact factor: 5.157

9.  Effect of cross-bridge kinetics on apparent Ca2+ sensitivity.

Authors:  P W Brandt; R N Cox; M Kawai; T Robinson
Journal:  J Gen Physiol       Date:  1982-06       Impact factor: 4.086

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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  208 in total

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3.  Influence of ionic strength on the actomyosin reaction steps in contracting skeletal muscle fibers.

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Journal:  Biophys J       Date:  2002-02       Impact factor: 4.033

7.  The biochemical kinetics underlying actin movement generated by one and many skeletal muscle myosin molecules.

Authors:  Josh E Baker; Christine Brosseau; Peteranne B Joel; David M Warshaw
Journal:  Biophys J       Date:  2002-04       Impact factor: 4.033

8.  Temperature dependence of the force-generating process in single fibres from frog skeletal muscle.

Authors:  G Piazzesi; M Reconditi; N Koubassova; V Decostre; M Linari; L Lucii; V Lombardi
Journal:  J Physiol       Date:  2003-03-28       Impact factor: 5.182

9.  The effect of polyethylene glycol on the mechanics and ATPase activity of active muscle fibers.

Authors:  M K Chinn; K H Myburgh; T Pham; K Franks-Skiba; R Cooke
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

10.  Reduced effect of pH on skinned rabbit psoas muscle mechanics at high temperatures: implications for fatigue.

Authors:  E Pate; M Bhimani; K Franks-Skiba; R Cooke
Journal:  J Physiol       Date:  1995-08-01       Impact factor: 5.182

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