Literature DB >> 10049330

The effect of thin filament activation on the attachment of weak binding cross-bridges: A two-dimensional x-ray diffraction study on single muscle fibers.

T Kraft1, S Xu, B Brenner, L C Yu.   

Abstract

To study possible structural changes in weak cross-bridge attachment to actin upon activation of the thin filament, two-dimensional (2D) x-ray diffraction patterns of skinned fibers from rabbit psoas muscle were recorded at low and high calcium concentration in the presence of saturating concentrations of MgATPgammaS, a nucleotide analog for weak binding states. We also studied 2D x-ray diffraction patterns recorded under relaxing conditions at an ionic strength above and below 50 mM, because it had been proposed from solution studies that reducing ionic strength below 50 mM also induces activation of the thin filament. For this project a novel preparation had to be established that allows recording of 2D x-ray diffraction patterns from single muscle fibers instead of natural fiber bundles. This was required to minimize substrate depletion or product accumulation within the fibers. When the calcium concentration was raised, the diffraction patterns recorded with MgATPgammaS revealed small changes in meridional reflections and layer line intensities that could be attributed in part to the effects of calcium binding to the thin filament (increase in I380, decrease in first actin layer line intensity, increase in I59) and in part to small structural changes of weakly attached cross-bridges (e.g., increase in I143 and I72). Calcium-induced small-scale structural rearrangements of cross-bridges weakly attached to actin in the presence of MgATPgammaS are consistent with our previous observation of reduced rate constants for attachment and detachment of cross-bridges with MgATPgammaS at high calcium. Yet, no evidence was found that weakly attached cross-bridges change their mode of attachment toward a stereospecific conformation when the actin filament is activated by adding calcium. Similarly, reducing ionic strength to less than 50 mM does not induce a transition from nonstereospecific to stereospecific attachment.

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Year:  1999        PMID: 10049330      PMCID: PMC1300126          DOI: 10.1016/S0006-3495(99)77309-1

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


  60 in total

1.  Steric-blocking by tropomyosin visualized in relaxed vertebrate muscle thin filaments.

Authors:  W Lehman; P Vibert; P Uman; R Craig
Journal:  J Mol Biol       Date:  1995-08-11       Impact factor: 5.469

2.  Parallel inhibition of active force and relaxed fiber stiffness by caldesmon fragments at physiological ionic strength and temperature conditions: additional evidence that weak cross-bridge binding to actin is an essential intermediate for force generation.

Authors:  T Kraft; J M Chalovich; L C Yu; B Brenner
Journal:  Biophys J       Date:  1995-06       Impact factor: 4.033

3.  Characterizations of cross-bridges in the presence of saturating concentrations of MgAMP-PNP in rabbit permeabilized psoas muscle.

Authors:  S M Frisbie; S Xu; J M Chalovich; L C Yu
Journal:  Biophys J       Date:  1998-06       Impact factor: 4.033

4.  X-ray diffraction studies of cross-bridges weakly bound to actin in relaxed skinned fibers of rabbit psoas muscle.

Authors:  S Xu; S Malinchik; D Gilroy; T Kraft; B Brenner; L C Yu
Journal:  Biophys J       Date:  1997-11       Impact factor: 4.033

5.  Structural changes in actin-tropomyosin during muscle regulation: computer modelling of low-angle X-ray diffraction data.

Authors:  H A al-Khayat; N Yagi; J M Squire
Journal:  J Mol Biol       Date:  1995-10-06       Impact factor: 5.469

6.  Millisecond time resolution electron cryo-microscopy of the M-ATP transient kinetic state of the acto-myosin ATPase.

Authors:  M Walker; J Trinick; H White
Journal:  Biophys J       Date:  1995-04       Impact factor: 4.033

Review 7.  The role of three-state docking of myosin S1 with actin in force generation.

Authors:  M A Geeves; P B Conibear
Journal:  Biophys J       Date:  1995-04       Impact factor: 4.033

Review 8.  The actomyosin interaction and its control by tropomyosin.

Authors:  K C Holmes
Journal:  Biophys J       Date:  1995-04       Impact factor: 4.033

9.  Equilibration and exchange of fluorescently labeled molecules in skinned skeletal muscle fibers visualized by confocal microscopy.

Authors:  T Kraft; M Messerli; B Rothen-Rutishauser; J C Perriard; T Wallimann; B Brenner
Journal:  Biophys J       Date:  1995-10       Impact factor: 4.033

10.  Elastic distortion of myosin heads and repriming of the working stroke in muscle.

Authors:  V Lombardi; G Piazzesi; M A Ferenczi; H Thirlwell; I Dobbie; M Irving
Journal:  Nature       Date:  1995-04-06       Impact factor: 49.962

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  16 in total

1.  Structural characterization of weakly attached cross-bridges in the A*M*ATP state in permeabilized rabbit psoas muscle.

Authors:  S Xu; J Gu; G Melvin; L C Yu
Journal:  Biophys J       Date:  2002-04       Impact factor: 4.033

2.  Mutation of the myosin converter domain alters cross-bridge elasticity.

Authors:  Jan Köhler; Gerhard Winkler; Imke Schulte; Tim Scholz; William McKenna; Bernhard Brenner; Theresia Kraft
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-19       Impact factor: 11.205

3.  Structural features of cross-bridges in isometrically contracting skeletal muscle.

Authors:  Theresia Kraft; Thomas Mattei; Ante Radocaj; Birgit Piep; Christoph Nocula; Markus Furch; Bernhard Brenner
Journal:  Biophys J       Date:  2002-05       Impact factor: 4.033

4.  Static and dynamic x-ray diffraction recordings from living mammalian and amphibian skeletal muscles.

Authors:  Hiroyuki Iwamoto; Jun'ichi Wakayama; Tetsuro Fujisawa; Naoto Yagi
Journal:  Biophys J       Date:  2003-10       Impact factor: 4.033

5.  Structural transients of contractile proteins upon sudden ATP liberation in skeletal muscle fibers.

Authors:  Jun'ichi Wakayama; Takumi Tamura; Naoto Yagi; Hiroyuki Iwamoto
Journal:  Biophys J       Date:  2004-07       Impact factor: 4.033

6.  Intensity of X-ray reflections from skeletal muscle thin filaments partially occupied with myosin heads: effect of cooperative binding.

Authors:  Takumi Tamura; Jun'ichi Wakayama; Tetsuro Fujisawa; Naoto Yagi; Hiroyuki Iwamoto
Journal:  J Muscle Res Cell Motil       Date:  2004       Impact factor: 2.698

7.  Initiation of the power stroke in muscle: insights from the phosphate analog AlF4.

Authors:  Theresia Kraft; Enke Mählmann; Thomas Mattei; Bernhard Brenner
Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-20       Impact factor: 11.205

8.  Force-generating cross-bridges during ramp-shaped releases: evidence for a new structural state.

Authors:  A Radocaj; T Weiss; W I Helsby; B Brenner; T Kraft
Journal:  Biophys J       Date:  2009-02-18       Impact factor: 4.033

9.  Dynamics of thin-filament activation in rabbit skeletal muscle fibers examined by time-resolved x-ray diffraction.

Authors:  Takumi Tamura; Jun'ichi Wakayama; Katsuaki Inoue; Naoto Yagi; Hiroyuki Iwamoto
Journal:  Biophys J       Date:  2009-02       Impact factor: 4.033

10.  X-ray diffraction analysis of the effects of myosin regulatory light chain phosphorylation and butanedione monoxime on skinned skeletal muscle fibers.

Authors:  Maki Yamaguchi; Masako Kimura; Zhao-Bo Li; Tetsuo Ohno; Shigeru Takemori; Joseph F Y Hoh; Naoto Yagi
Journal:  Am J Physiol Cell Physiol       Date:  2016-02-24       Impact factor: 4.249

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