Literature DB >> 3972790

Skeletal muscle myosin subfragment-1 induces bundle formation by actin filaments.

T Ando, D Scales.   

Abstract

As is well known, the light scattering intensity of F-actin solutions increases immediately upon formation of the rigor complex with subfragment-1 (S-1). We have found that after the initial rise in scattering, there is a further gradual increase in scattering (we call it "super-opalescence"). Fluorescence and electron microscopic observations of acto-S-1 solutions showed that super-opalescence results from formation of actin filament bundles once S-1 binds to F-actin. The actin bundles possessed transverse stripes with a periodicity of about 350 A, which suggested that in the bundles actin filaments are arranged in parallel register. The rate of the initial process of bundle formation (i.e. side-by-side dimerization) could be approximately estimated by measuring the initial rate of super-opalescence (V0). V0 had a maximum (V0m) at a molar ratio of S-1 to actin of 1;6-1;7, regardless of the actin concentration, pH (6-8.5), Mg2+ concentration (up to 5 mM), or ionic strength (up to 0.3 M KC1). Lower pH, higher Mg2+ concentration, and higher ionic strength increased V0m; V0 was proportional to the square of the actin concentration, regardless of the solution conditions.

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Year:  1985        PMID: 3972790

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  16 in total

1.  Kinetic studies on the effects of ADP and ionic strength on the interaction between myosin subfragment-1 and actin: implications for load-sensitivity and regulation of the crossbridge cycle.

Authors:  P B Conibear
Journal:  J Muscle Res Cell Motil       Date:  1999-11       Impact factor: 2.698

2.  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

3.  Interhead distances in myosin attached to F-actin estimated by fluorescence energy transfer spectroscopy.

Authors:  S Ishiwata; M Miki; I Shin; T Funatsu; K Yasuda; C G dos Remedios
Journal:  Biophys J       Date:  1997-08       Impact factor: 4.033

4.  The molecular origin of birefringence in skeletal muscle. Contribution of myosin subfragment S-1.

Authors:  H M Jones; R J Baskin; Y Yeh
Journal:  Biophys J       Date:  1991-11       Impact factor: 4.033

5.  Differential Behavior of Heavy Meromyosin and Heavy Meromyosin Subfragment One toward A Monomeric Actin Derivative.

Authors:  L D Burtnick
Journal:  Biophys J       Date:  1986-01       Impact factor: 4.033

6.  ATPase kinetics of the Dictyostelium discoideum myosin II motor domain.

Authors:  P A Kuhlman; C R Bagshaw
Journal:  J Muscle Res Cell Motil       Date:  1998-06       Impact factor: 2.698

Review 7.  Fluorescence resonance energy transfer measurements of distances in actin and myosin. A critical evaluation.

Authors:  C G dos Remedios; M Miki; J A Barden
Journal:  J Muscle Res Cell Motil       Date:  1987-04       Impact factor: 2.698

8.  A single myosin head can be cross-linked to the N termini of two adjacent actin monomers.

Authors:  N Bonafé; P Chaussepied
Journal:  Biophys J       Date:  1995-04       Impact factor: 4.033

9.  Orientational distribution of spin-labeled actin oriented by flow.

Authors:  E M Ostap; T Yanagida; D D Thomas
Journal:  Biophys J       Date:  1992-10       Impact factor: 4.033

10.  Rotational dynamics of spin-labeled F-actin during activation of myosin S1 ATPase using caged ATP.

Authors:  E M Ostap; D D Thomas
Journal:  Biophys J       Date:  1991-06       Impact factor: 4.033

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