Literature DB >> 1886072

Cross-bridge kinetics in the presence of MgADP investigated by photolysis of caged ATP in rabbit psoas muscle fibres.

J A Dantzig1, M G Hibberd, D R Trentham, Y E Goldman.   

Abstract

1. The interaction between MgADP and rigor cross-bridges in glycerol-extracted single fibres from rabbit psoas muscle has been investigated using laser pulse photolysis of caged ATP (P3-1(2-nitrophenyl)ethyladenosine 5'-triphosphate) in the presence of MgADP and following small length changes applied to the rigor fibre. 2. Addition of 465 microM-MgADP to a rigor fibre caused rigor tension to decrease by 15.3 +/- 0.7% (S.E.M., n = 24 trials in thirteen fibres). The half-saturation value for this tension reduction was 18 +/- 4 microM (n = 23, thirteen fibres). 3. Relaxation from rigor by photolysis of caged ATP in the absence of Ca2+ was markedly slowed by inclusion of 20 microM-2 mM-MgADP in the photolysis medium. 4. Four phases of tension relaxation occurred with MgADP in the medium: at, a quick partial relaxation (in pre-stretch fibres); bt, a slowing of relaxation or a rise in tension for 50-100 ms; ct, a sudden acceleration of relaxation; and dt, a final, nearly exponential relaxation. 5. Experiments at varied MgATP and MgADP concentrations suggested that phase at is due to MgATP binding to nucleotide-free cross-bridges. 6. Phase bt was abbreviated by including 1-20 mM-orthophosphate (Pi) in the photolysis medium, or by applying quick stretches before photolysis or during phase bt. These results suggest that phases bt and ct are complex processes involving ADP dissociation, cross-bridge reattachment and co-operative detachment involving filament sliding and the Ca(2+)-regulatory system. 7. Stretching relaxed muscle fibres to 3.2-3.4 microns striation spacing followed by ATP removal and release of the rigor fibre until tension fell below the relaxed level allowed investigation of the strain dependence of relaxation in the regions of negative cross-bridge strain. In the presence of 50 microM-2 mM-MgADP and either 10 mM-Pi or 20 mM-2,3-butanedione monoxime, relaxation following photolysis of caged ATP was 6- to 8-fold faster for negatively strained cross-bridges than for positively strained ones. This marked strain dependence of cross-bridge detachment is predicted from the model of A. F. Huxley (1957). 8. In the presence of Ca2+, activation of contraction following photolysis of caged ATP was slowed by inclusion of 20-500 microM-MgADP in the medium. An initial decrease in tension related to cross-bridge detachment by MgATP was markedly suppressed in the presence of MgADP. 9. Ten millimolar Pi partly suppressed active tension generation in the presence of MgADP.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1886072      PMCID: PMC1181346          DOI: 10.1113/jphysiol.1991.sp018405

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


  46 in total

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Authors:  A V HILL
Journal:  Proc R Soc Lond B Biol Sci       Date:  1964-01-14

2.  Muscle structure and theories of contraction.

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

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Authors:  I Matsubara; N Yagi; H Hashizume
Journal:  Nature       Date:  1975-06-26       Impact factor: 49.962

4.  A quantitative comparison between the energy liberated and the work performed by the isolated sartorius muscle of the frog.

Authors:  W O Fenn
Journal:  J Physiol       Date:  1923-12-28       Impact factor: 5.182

5.  X-ray evidence for radial cross-bridge movement and for the sliding filament model in actively contracting skeletal muscle.

Authors:  J C Haselgrove; H E Huxley
Journal:  J Mol Biol       Date:  1973-07-15       Impact factor: 5.469

6.  Muscular contraction.

Authors:  A F Huxley
Journal:  J Physiol       Date:  1974-11       Impact factor: 5.182

7.  The nucleotide complexes of myosin in glycerol-extracted muscle fibres.

Authors:  S Marston
Journal:  Biochim Biophys Acta       Date:  1973-05-30

Review 8.  The mechanism of muscular contraction.

Authors:  H E Huxley
Journal:  Science       Date:  1969-06-20       Impact factor: 47.728

9.  Proposed mechanism of force generation in striated muscle.

Authors:  A F Huxley; R M Simmons
Journal:  Nature       Date:  1971-10-22       Impact factor: 49.962

10.  The role of orthophosphate in crossbridge kinetics in chemically skinned rabbit psoas fibres as detected with sinusoidal and step length alterations.

Authors:  M Kawai
Journal:  J Muscle Res Cell Motil       Date:  1986-10       Impact factor: 2.698

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  81 in total

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

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3.  Measurement of nucleotide exchange rate constants in single rabbit soleus myofibrils during shortening and lengthening using a fluorescent ATP analog.

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Review 5.  Cooperative behavior of molecular motors.

Authors:  Karen C Vermeulen; Ger J M Stienen; Christoph F Schmid
Journal:  J Muscle Res Cell Motil       Date:  2002       Impact factor: 2.698

6.  Structural transients of contractile proteins upon sudden ATP liberation in skeletal muscle fibers.

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Journal:  Biophys J       Date:  2004-07       Impact factor: 4.033

7.  An integrated in vitro and in situ study of kinetics of myosin II from frog skeletal muscle.

Authors:  R Elangovan; M Capitanio; L Melli; F S Pavone; V Lombardi; G Piazzesi
Journal:  J Physiol       Date:  2011-12-23       Impact factor: 5.182

Review 8.  Force and power generating mechanism(s) in active muscle as revealed from temperature perturbation studies.

Authors:  K W Ranatunga
Journal:  J Physiol       Date:  2010-10-01       Impact factor: 5.182

9.  A metabolite-sensitive, thermodynamically constrained model of cardiac cross-bridge cycling: implications for force development during ischemia.

Authors:  Kenneth Tran; Nicolas P Smith; Denis S Loiselle; Edmund J Crampin
Journal:  Biophys J       Date:  2010-01-20       Impact factor: 4.033

10.  Relaxation from rigor of skinned trabeculae of the guinea pig induced by laser photolysis of caged ATP.

Authors:  H Martin; R J Barsotti
Journal:  Biophys J       Date:  1994-04       Impact factor: 4.033

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