Literature DB >> 3524992

The mechanism of muscle contraction.

R Cooke.   

Abstract

Knowledge of the mechanism of contraction has been obtained from studies of the interaction of actin and myosin in solution, from an elucidation of the structure of muscle fibers, and from measurements of the mechanics and energetics of fiber contraction. Many of the states and the transition rates between them have been established for the hydrolysis of ATP by actin and myosin subfragments in solution. A major goal is to now understand how the kinetics of this interaction are altered when it occurs in the organized array of the myofibril. Early work on the structure of muscle suggested that changes in the orientation of myosin cross-bridges were responsible for the generation of force. More recently, fluorescent and paramagnetic probes attached to the cross-bridges have suggested that at least some domains of the cross-bridges do not change orientation during force generation. A number of properties of active cross-bridges have been defined by measurements of steady state contractions of fibers and by the transients which follow step changes in fiber length or tension. Taken together these studies have provided firm evidence that force is generated by a cyclic interaction in which a myosin cross-bridge attaches to actin, exerts force through a "powerstroke" of 12 nm, and is then released by the binding of ATP. The mechanism of this interaction at the molecular level remains unknown.

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Year:  1986        PMID: 3524992     DOI: 10.3109/10409238609113609

Source DB:  PubMed          Journal:  CRC Crit Rev Biochem        ISSN: 0045-6411


  120 in total

1.  Interaction of myosin with F-actin: time-dependent changes at the interface are not slow.

Authors:  J Van Dijk; F Céline; T Barman; P Chaussepied
Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

Review 2.  The structural basis of muscle contraction.

Authors:  K C Holmes; M A Geeves
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-04-29       Impact factor: 6.237

3.  Independent mobility of catalytic and regulatory domains of myosin heads.

Authors:  B Adhikari; K Hideg; P G Fajer
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-02       Impact factor: 11.205

4.  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

5.  The orientation of transition moments of dye molecules used in fluorescence studies of muscle systems.

Authors:  U A van der Heide; B Orbons; H C Gerritsen; Y K Levine
Journal:  Eur Biophys J       Date:  1992       Impact factor: 1.733

6.  Polarized fluorescence depletion reports orientation distribution and rotational dynamics of muscle cross-bridges.

Authors:  Marcus G Bell; Robert E Dale; Uulke A van der Heide; Yale E Goldman
Journal:  Biophys J       Date:  2002-08       Impact factor: 4.033

7.  Rotation of the stalk/neck and one head in a new crystal structure of the kinesin motor protein, Ncd.

Authors:  Mikyung Yun; C Eric Bronner; Cheon-Gil Park; Sun-Shin Cha; Hee-Won Park; Sharyn A Endow
Journal:  EMBO J       Date:  2003-10-15       Impact factor: 11.598

8.  Brush border myosin-I structure and ADP-dependent conformational changes revealed by cryoelectron microscopy and image analysis.

Authors:  J D Jontes; R A Milligan
Journal:  J Cell Biol       Date:  1997-11-03       Impact factor: 10.539

9.  Myosin cross-bridge orientation in rigor and in the presence of nucleotide studied by electron spin resonance.

Authors:  K Ajtai; A R French; T P Burghardt
Journal:  Biophys J       Date:  1989-09       Impact factor: 4.033

10.  The essential light chain is required for full force production by skeletal muscle myosin.

Authors:  P VanBuren; G S Waller; D E Harris; K M Trybus; D M Warshaw; S Lowey
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-20       Impact factor: 11.205

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