Literature DB >> 27763660

Minimum number of myosin motors accounting for shortening velocity under zero load in skeletal muscle.

Luca Fusi1, Valentina Percario2, Elisabetta Brunello2, Marco Caremani2, Pasquale Bianco2, Joseph D Powers2, Massimo Reconditi2, Vincenzo Lombardi2, Gabriella Piazzesi2.   

Abstract

KEY POINTS: Myosin filament mechanosensing determines the efficiency of the contraction by adapting the number of switched ON motors to the load. Accordingly, the unloaded shortening velocity (V0 ) is already set at the end of latency relaxation (LR), ∼10 ms after the start of stimulation, when the myosin filament is still in the OFF state. Here the number of actin-attached motors per half-myosin filament (n) during V0 shortening imposed either at the end of LR or at the plateau of the isometric contraction is estimated from the relation between half-sarcomere compliance and force during the force redevelopment after shortening. The value of n decreases progressively with shortening and, during V0 shortening starting at the end of LR, is 1-4. Reduction of n is accounted for by a constant duty ratio of 0.05 and a parallel switching OFF of motors, explaining the very low rate of ATP utilization found during unloaded shortening. ABSTRACT: The maximum velocity at which a skeletal muscle can shorten (i.e. the velocity of sliding between the myosin filament and the actin filament under zero load, V0 ) is already set at the end of the latency relaxation (LR) preceding isometric force generation, ∼10 ms after the start of electrical stimulation in frog muscle fibres at 4°C. At this time, Ca2+ -induced activation of the actin filament is maximal, while the myosin filament is in the OFF state characterized by most of the myosin motors lying on helical tracks on the filament surface, making them unavailable for actin binding and ATP hydrolysis. Here, the number of actin-attached motors per half-thick filament during V0 shortening (n) is estimated by imposing, on tetanized single fibres from Rana esculenta (at 4°C and sarcomere length 2.15 μm), small 4 kHz oscillations and determining the relation between half-sarcomere (hs) compliance and force during the force development following V0 shortening. When V0 shortening is superimposed on the maximum isometric force T0 , n decreases progressively with the increase of shortening (range 30-80 nm per hs) and, when V0 shortening is imposed at the end of LR, n can be as low as 1-4. Reduction of n is accounted for by a constant duty ratio of the myosin motor of ∼0.05 and a parallel switching OFF of the thick filament, providing an explanation for the very low rate of ATP utilization during extended V0 shortening.
© 2016 The Authors. The Journal of Physiology © 2016 The Physiological Society.

Entities:  

Keywords:  maximum shortening velocity; muscle mechanics; muscle myosin

Mesh:

Substances:

Year:  2016        PMID: 27763660      PMCID: PMC5309372          DOI: 10.1113/JP273299

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


  34 in total

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2.  The contractile response during steady lengthening of stimulated frog muscle fibres.

Authors:  V Lombardi; G Piazzesi
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3.  Tension responses to sudden length change in stimulated frog muscle fibres near slack length.

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4.  Energetic aspects of muscle contraction.

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6.  Motion of myosin head domains during activation and force development in skeletal muscle.

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7.  Variation in myoplasmic Ca2+ concentration during contraction and relaxation studied by the indicator fluo-3 in frog muscle fibres.

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8.  Three-dimensional structure of vertebrate cardiac muscle myosin filaments.

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Authors:  Luca Fusi; Zhe Huang; Malcolm Irving
Journal:  Biophys J       Date:  2015-08-18       Impact factor: 4.033

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  19 in total

1.  CaATP prolongs strong actomyosin binding and promotes futile myosin stroke.

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2.  A mechanical model of the half-sarcomere which includes the contribution of titin.

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5.  Force-Dependent Recruitment from the Myosin Off State Contributes to Length-Dependent Activation.

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6.  The force and stiffness of myosin motors in the isometric twitch of a cardiac trabecula and the effect of the extracellular calcium concentration.

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7.  Effects of mavacamten on Ca2+ sensitivity of contraction as sarcomere length varied in human myocardium.

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Review 8.  Straightening Out the Elasticity of Myosin Cross-Bridges.

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Review 10.  Regulation of Contraction by the Thick Filaments in Skeletal Muscle.

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