Literature DB >> 6607073

Optical depolarization changes on the diffraction pattern in the transition of skinned muscle fibers from relaxed to rigor state.

Y Yeh, M E Corcoran, R J Baskin, R L Lieber.   

Abstract

Light diffraction spectra from single or small bundles of skinned striated muscle fibers show large changes in polarization properties when muscles are placed into rigor. The technique of combining optical diffraction and ellipsometry measurements has previously been shown by Yeh and Pinsky to be a sensitive probe of periodic anisotropic regions of the fiber. In the present work, using this method, the observed spectrum shows marked decrease in the measured phase angle, delta, as the fiber approaches the rigor state. The degree of phase angle change is a function of sarcomere length: Maximum overlap of approximately 2.3 microns gives the most change in delta a delta delta R-R approximately 35 degrees decrease for a bundle of three fibers. At a sarcomere length of 2.9 microns this delta delta R-R value is only 10 degrees. At a nonoverlapping length of approximately 3.8 microns, delta does not vary at all upon the removal of ATP. The rigor state was confirmed by stiffness measurements made after small-amplitude (0.75%), quick length changes. Upon re-relaxation, the stiffness of the skinned fiber decreased to the value of the resting state (4 mM ATP) and the phase angle delta returned to its original value. A model based on either anisotropic subunit-2 (S-2) movements or other cross-bridge-related structural anisotropy (form birefringence) changes during the relaxed-rigor transition is suggested.

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Year:  1983        PMID: 6607073      PMCID: PMC1434851          DOI: 10.1016/S0006-3495(83)84308-2

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


  18 in total

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Authors:  R J Podolsky; H St Onge; L Yu; R W Lymn
Journal:  Proc Natl Acad Sci U S A       Date:  1976-03       Impact factor: 11.205

2.  Tension responses to sudden length change in stimulated frog muscle fibres near slack length.

Authors:  L E Ford; A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

3.  Mechanism of adenosine triphosphate hydrolysis by actomyosin.

Authors:  R W Lymn; E W Taylor
Journal:  Biochemistry       Date:  1971-12-07       Impact factor: 3.162

4.  The effect of calcium on the force-velocity relation of briefly glycerinated frog muscle fibres.

Authors:  F J Julian
Journal:  J Physiol       Date:  1971-10       Impact factor: 5.182

5.  Helicoids in the T system and striations of frog skeletal muscle fibers seen by high voltage electron microscopy.

Authors:  L D Peachey; B R Eisenberg
Journal:  Biophys J       Date:  1978-05       Impact factor: 4.033

6.  Millisecond time-resolved changes in x-ray reflections from contracting muscle during rapid mechanical transients, recorded using synchrotron radiation.

Authors:  H E Huxley; R M Simmons; A R Faruqi; M Kress; J Bordas; M H Koch
Journal:  Proc Natl Acad Sci U S A       Date:  1981-04       Impact factor: 11.205

7.  Human skeletal muscle: analysis of Ca2+ regulation in skinned fibers using caffeine.

Authors:  D S Wood
Journal:  Exp Neurol       Date:  1978-01-15       Impact factor: 5.330

8.  Induced changes in orientation of the cross-bridges of glycerinated insect flight muscle.

Authors:  M K Reedy; K C Holmes; R T Tregear
Journal:  Nature       Date:  1965-09-18       Impact factor: 49.962

9.  Tension development in highly stretched vertebrate muscle fibres.

Authors:  A M Gordon; A F Huxley; F J Julian
Journal:  J Physiol       Date:  1966-05       Impact factor: 5.182

10.  Use of fluorescence polarization to observe changes in attitude of S-1 moieties in muscle fibers.

Authors:  T Nihei; R A Mendelson; J Botts
Journal:  Biophys J       Date:  1974-03       Impact factor: 4.033

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  10 in total

1.  Diffraction ellipsometry studies of osmotically compressed muscle fibers.

Authors:  W L Kerr; R J Baskin; Y Yeh
Journal:  Pflugers Arch       Date:  1990-08       Impact factor: 3.657

2.  Optical ellipsometry measurements on the diffraction patterns from single fibers.

Authors:  R J Baskin; K Burton; J S Chen; Y Yeh
Journal:  Biophys J       Date:  1986-01       Impact factor: 4.033

3.  Polarization changes in light diffracted from contracting muscle fibers.

Authors:  A F Leung; M K Cheung
Journal:  Cell Biophys       Date:  1987-04

4.  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

5.  Decrease in light diffraction intensity of contracting muscle fibres.

Authors:  A F Leung; M K Cheung
Journal:  Eur Biophys J       Date:  1988       Impact factor: 1.733

6.  Theory of optical ellipsometric measurements from muscle diffraction studies.

Authors:  Y Yeh; R J Baskin
Journal:  Biophys J       Date:  1988-08       Impact factor: 4.033

7.  Optical ellipsometry on the diffraction order of skinned fibers. pH-induced rigor effects.

Authors:  Y Yeh; R J Baskin; K Burton; J S Chen
Journal:  Biophys J       Date:  1987-03       Impact factor: 4.033

8.  Crossbridge activity monitored from the state of polarization of light diffracted by activated frog muscle fibres.

Authors:  K Burton; R J Baskin; Y Yeh
Journal:  J Muscle Res Cell Motil       Date:  1990-06       Impact factor: 2.698

9.  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

10.  Depolarization spectrum of diffracted light from muscle fiber. The intrinsic anisotropy component.

Authors:  Y Yeh; R J Baskin; R A Brown; K Burton
Journal:  Biophys J       Date:  1985-05       Impact factor: 4.033

  10 in total

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