Literature DB >> 8534820

Sliding distance per ATP molecule hydrolyzed by myosin heads during isotonic shortening of skinned muscle fibers.

H Higuchi1, Y E Goldman.   

Abstract

We measured isotonic sliding distance of single skinned fibers from rabbit psoas muscle when known and limited amounts of ATP were made available to the contractile apparatus. The fibers were immersed in paraffin oil at 20 degrees C, and laser pulse photolysis of caged ATP within the fiber initiated the contraction. The amount of ATP released was measured by photolyzing 3H-ATP within fibers, separating the reaction products by high-pressure liquid chromatography, and then counting the effluent peaks by liquid scintillation. The fiber stiffness was monitored to estimate the proportion of thick and thin filament sites interacting during filament sliding. The interaction distance, Di, defined as the sliding distance while a myosin head interacts with actin in the thin filament per ATP molecule hydrolyzed, was estimated from the shortening distance, the number of ATP molecules hydrolyzed by the myosin heads, and the stiffness. Di increased from 11 to 60 nm as the isotonic tension was reduced from 80% to 6% of the isometric tension. Velocity and Di increased with the concentration of ATP available. As isotonic load was increased, the interaction distance decreased linearly with decrease of the shortening velocity and extrapolated to 8 nm at zero velocity. Extrapolation of the relationship between Di and velocity to saturating ATP concentration suggests that Di reaches 100-190 nm at high shortening velocity. The interaction distance corresponds to the sliding distance while cross-bridges are producing positive (working) force plus the distance while they are dragging (producing negative forces). The results indicate that the working and drag distances increase as the velocity increases. Because Di is larger than the size of either the myosin head or the actin monomer, the results suggest that for each ATPase cycle, a myosin head interacts mechanically with several actin monomers either while working or while producing drag.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8534820      PMCID: PMC1236380          DOI: 10.1016/S0006-3495(95)80020-2

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


  65 in total

1.  INFLUENCE OF OSMOTIC STRENGTH ON CROSS-SECTION AND VOLUME OF ISOLATED SINGLE MUSCLE FIBRES.

Authors:  J R BLINKS
Journal:  J Physiol       Date:  1965-03       Impact factor: 5.182

2.  The myosin step size: measurement of the unit displacement per ATP hydrolyzed in an in vitro assay.

Authors:  Y Y Toyoshima; S J Kron; J A Spudich
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

3.  Mechanochemical coupling in actomyosin energy transduction studied by in vitro movement assay.

Authors:  Y Harada; K Sakurada; T Aoki; D D Thomas; T Yanagida
Journal:  J Mol Biol       Date:  1990-11-05       Impact factor: 5.469

4.  The chemical energetics of muscle contraction. II. The chemistry, efficiency and power of maximally working sartorius muscles. Appendix. Free energy and enthalpy of atp hydrolysis in the sarcoplasm.

Authors:  M J Kushmerick; R E Davies
Journal:  Proc R Soc Lond B Biol Sci       Date:  1969-12-23

5.  Evidence for a complex between myosin and ADP in relaxed muscle fibres.

Authors:  S B Marston; R T Tregear
Journal:  Nat New Biol       Date:  1972-01-05

6.  Mechanism of adenosine triphosphate hydrolysis by actomyosin.

Authors:  R W Lymn; E W Taylor
Journal:  Biochemistry       Date:  1971-12-07       Impact factor: 3.162

Review 7.  The mechanism of muscular contraction.

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

8.  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

9.  Induced changes in orientation of the cross-bridges of glycerinated insect flight muscle.

Authors:  M K Reedy; K C Holmes; R T Tregear
Journal:  Nature       Date:  1965-09-18       Impact factor: 49.962

10.  Tension development in highly stretched vertebrate muscle fibres.

Authors:  A M Gordon; A F Huxley; F J Julian
Journal:  J Physiol       Date:  1966-05       Impact factor: 5.182

View more
  17 in total

1.  Detection of fluorescently labeled actin-bound cross-bridges in actively contracting myofibrils.

Authors:  W C Cooper; L R Chrin; C L Berger
Journal:  Biophys J       Date:  2000-03       Impact factor: 4.033

2.  Cross-bridge attachment during high-speed active shortening of skinned fibers of the rabbit psoas muscle: implications for cross-bridge action during maximum velocity of filament sliding.

Authors:  R Stehle; B Brenner
Journal:  Biophys J       Date:  2000-03       Impact factor: 4.033

Review 3.  Mechanics and models of the myosin motor.

Authors:  A F Huxley
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-04-29       Impact factor: 6.237

4.  Measured and modeled properties of mammalian skeletal muscle: III. the effects of stimulus frequency on stretch-induced force enhancement and shortening-induced force depression.

Authors:  I E Brown; G E Loeb
Journal:  J Muscle Res Cell Motil       Date:  2000-01       Impact factor: 2.698

5.  Structural kinetics of myosin by transient time-resolved FRET.

Authors:  Yuri E Nesmelov; Roman V Agafonov; Igor V Negrashov; Sarah E Blakely; Margaret A Titus; David D Thomas
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-18       Impact factor: 11.205

6.  The biphasic force-velocity relationship in frog muscle fibres and its evaluation in terms of cross-bridge function.

Authors:  K A Edman; A Månsson; C Caputo
Journal:  J Physiol       Date:  1997-08-15       Impact factor: 5.182

7.  Kinetics of force generation by single kinesin molecules activated by laser photolysis of caged ATP.

Authors:  H Higuchi; E Muto; Y Inoue; T Yanagida
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-29       Impact factor: 11.205

8.  Surfing along Filopodia: A Particle Transport Revealed by Molecular-Scale Fluctuation Analyses.

Authors:  Felix Kohler; Alexander Rohrbach
Journal:  Biophys J       Date:  2015-05-05       Impact factor: 4.033

Review 9.  Stiffness, working stroke, and force of single-myosin molecules in skeletal muscle: elucidation of these mechanical properties via nonlinear elasticity evaluation.

Authors:  Motoshi Kaya; Hideo Higuchi
Journal:  Cell Mol Life Sci       Date:  2013-05-18       Impact factor: 9.261

10.  Mechanochemical coupling in muscle: attempts to measure simultaneously shortening and ATPase rates in myofibrils.

Authors:  C Lionne; F Travers; T Barman
Journal:  Biophys J       Date:  1996-02       Impact factor: 4.033

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.