Literature DB >> 16172377

Effect of temperature on the working stroke of muscle myosin.

V Decostre1, P Bianco, V Lombardi, G Piazzesi.   

Abstract

Muscle contraction is due to myosin motors that transiently attach with their globular head to an actin filament and generate force. After a sudden reduction of the load below the maximum isometric force (T0), the attached myosin heads execute an axial movement (the working stroke) that drives the sliding of the actin filament toward the center of the sarcomere by an amount that is larger at lower load and is 11 nm near zero load. Here, we show that an increase in temperature from 2 to 17 degrees C, which increases the average isometric force per attached myosin head by 60%, does not affect the amount of filament sliding promoted by a reduction in force from T0 to 0.7T0, whereas it reduces the sliding under low load by 2.5 nm. These results exclude the possibility that the myosin working stroke is due to the release of the mechanical energy stored in the initial endothermic force-generating process and show that, at higher temperatures, the working stroke energy is greater because of higher force, although the stroke length is smaller at low load. We conclude the following: (i) the working stroke is made by a series of state transitions in the attached myosin head; (ii) the temperature increases the probability for the first transition, competent for isometric force generation; and (iii) the temperature-dependent rise in work at high load can be accounted for by the larger free energy drop that explains the rise in isometric force.

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Year:  2005        PMID: 16172377      PMCID: PMC1236584          DOI: 10.1073/pnas.0506795102

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  27 in total

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6.  Transient tension changes initiated by laser temperature jumps in rabbit psoas muscle fibres.

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9.  Structure of the actin-myosin complex and its implications for muscle contraction.

Authors:  I Rayment; H M Holden; M Whittaker; C B Yohn; M Lorenz; K C Holmes; R A Milligan
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Authors:  Y Zhao; M Kawai
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  45 in total

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Review 3.  Force and power generating mechanism(s) in active muscle as revealed from temperature perturbation studies.

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4.  Orthovanadate and orthophosphate inhibit muscle force via two different pathways of the myosin ATPase cycle.

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5.  Single-molecule measurement of the stiffness of the rigor myosin head.

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6.  Residual force enhancement in myofibrils and sarcomeres.

Authors:  V Joumaa; T R Leonard; W Herzog
Journal:  Proc Biol Sci       Date:  2008-06-22       Impact factor: 5.349

Review 7.  Temperature change as a probe of muscle crossbridge kinetics: a review and discussion.

Authors:  R C Woledge; C J Barclay; N A Curtin
Journal:  Proc Biol Sci       Date:  2009-04-08       Impact factor: 5.349

8.  Mechanistic role of movement and strain sensitivity in muscle contraction.

Authors:  Julien S Davis; Neal D Epstein
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-26       Impact factor: 11.205

9.  The effect of myofilament compliance on kinetics of force generation by myosin motors in muscle.

Authors:  M Linari; G Piazzesi; V Lombardi
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10.  The non-linear elasticity of the muscle sarcomere and the compliance of myosin motors.

Authors:  Luca Fusi; Elisabetta Brunello; Massimo Reconditi; Gabriella Piazzesi; Vincenzo Lombardi
Journal:  J Physiol       Date:  2013-12-16       Impact factor: 5.182

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