Literature DB >> 1760508

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

H M Jones1, R J Baskin, Y Yeh.   

Abstract

The state of optical polarization of He-Ne laser light diffracted by single skinned frog skeletal muscle fibers has been determined after decoration of the thin filaments of rigor fibers with exogenous S-1. Light on the first diffraction order was analyzed using optical ellipsometry for changes occurring in total birefringence (delta nT) and total differential field ratio (rT) and the experimental results compared with theoretical predictions. Fibers were examined with SDS-gel electrophoresis and electron microscopy as independent assays of S-1 binding. The binding of S-1 to the thin filaments caused a significant increase in rT and a small but significant decrease in delta nT. Release of bound exogenous S-1 with magnesium pyrophosphate demonstrated that the effect of S-1 on the optical parameters was reversible and both electrophoresis and electron microscopy demonstrated the presence of S-1 specifically bound to the thin filaments. Model simulations based on the theory of Yeh, Y., and R. Baskin (1988. Biophys. J. 54:205-218) showed that the values of delta nT and rT were sensitive to the axial bonding angle of exogenous S-1 as well as to the volume fraction of added S-1. Analysis of the data in light of the model showed that an average axial S-1 binding angle of 68 degrees +/- 7 degrees best fit the data.

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Year:  1991        PMID: 1760508      PMCID: PMC1260176          DOI: 10.1016/S0006-3495(91)82156-7

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


  36 in total

1.  Photon correlation spectroscopy of the polarization signal from single muscle fibres.

Authors:  Y Yeh; R J Baskin; S Shen; M Jones
Journal:  J Muscle Res Cell Motil       Date:  1990-04       Impact factor: 2.698

2.  Optical depolarization changes in single, skinned muscle fibers. Evidence for cross-bridge involvement.

Authors:  R J Baskin; Y Yeh; K Burton; J S Chen; M Jones
Journal:  Biophys J       Date:  1986-07       Impact factor: 4.033

3.  Structure of the actin-myosin complex in the presence of ATP.

Authors:  R Craig; L E Greene; E Eisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

4.  Transient electrical birefringence characterization of heavy meromyosin.

Authors:  S Highsmith; D Eden
Journal:  Biochemistry       Date:  1985-08-27       Impact factor: 3.162

5.  Silver stain for proteins in polyacrylamide gels: a modified procedure with enhanced uniform sensitivity.

Authors:  J H Morrissey
Journal:  Anal Biochem       Date:  1981-11-01       Impact factor: 3.365

6.  Preparation of myosin and its subfragments from rabbit skeletal muscle.

Authors:  S S Margossian; S Lowey
Journal:  Methods Enzymol       Date:  1982       Impact factor: 1.600

7.  Submillisecond rotational dynamics of spin-labeled myosin heads in myofibrils.

Authors:  D D Thomas; S Ishiwata; J C Seidel; J Gergely
Journal:  Biophys J       Date:  1980-12       Impact factor: 4.033

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

Authors:  T Ando; D Scales
Journal:  J Biol Chem       Date:  1985-02-25       Impact factor: 5.157

9.  Bundling of myosin subfragment-1-decorated actin filaments.

Authors:  T Ando
Journal:  J Mol Biol       Date:  1987-05-20       Impact factor: 5.469

10.  Local melting in the subfragment-2 region of myosin in activated muscle and its correlation with contractile force.

Authors:  H Ueno; W F Harrington
Journal:  J Mol Biol       Date:  1986-07-05       Impact factor: 5.469

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  1 in total

1.  Rigorous analysis of light diffraction ellipsometry by striated muscle fibers.

Authors:  E Sidick; R J Baskin; Y Yeh; A Knoesen
Journal:  Biophys J       Date:  1994-06       Impact factor: 4.033

  1 in total

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