Literature DB >> 1657230

Orientational disorder and motion of weakly attached cross-bridges.

P G Fajer1, E A Fajer, M Schoenberg, D D Thomas.   

Abstract

In a relaxed muscle fiber at low ionic strength, the cross-bridges may well be in states comparable to the one that precedes the cross-bridge power stroke (Schoenberg, M. 1988. Adv. Exp. Med. Biol. 226:189-202). Using electron paramagnetic resonance (EPR) and (saturation transfer) electron paramagnetic resonance (ST-EPR) techniques on fibers labeled with maleimide spin label, under low ionic strength conditions designed to produce a majority of weakly-attached heads, we have established that (a) relaxed labeled fibers show a speed dependence of chord stiffness identical to that of unlabeled, relaxed fibers, suggesting similar rapid dissociation and reassociation of cross-bridges; (b) the attached relaxed heads at low ionic strength are nearly as disordered as in relaxation at physiological ionic strength where most of the heads are detached from actin; and (c) the microsecond rotational mobility of the relaxed heads was only slightly restricted compared to normal ionic strength, implying great motional freedom despite attachment. The differences in head mobility between low and normal ionic strength scale with filament overlap and are thus due to acto-myosin interactions. The spectra can be modeled in terms of two populations: one identical to relaxed heads at normal ionic strength (83%), the other representing a more oriented population of heads (17%). The spectrum of the latter is centered at approximately the same angle as the spectrum in rigor but exhibits larger (40 degrees) axial probe disorder with respect to the fiber axis. Alternatively, assuming that the chord stiffness is proportional to the fraction of attached crossbridges, the attached fraction must be even more disordered than 400, with rotational mobility nearly as great as for detached cross-bridges.

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Year:  1991        PMID: 1657230      PMCID: PMC1260107          DOI: 10.1016/S0006-3495(91)82093-8

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


  35 in total

1.  Photolysis of a photolabile precursor of ATP (caged ATP) induces microsecond rotational motions of myosin heads bound to actin.

Authors:  C L Berger; E C Svensson; D D Thomas
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

Review 2.  Spectroscopic probes of muscle cross-bridge rotation.

Authors:  D D Thomas
Journal:  Annu Rev Physiol       Date:  1987       Impact factor: 19.318

3.  Relaxation of muscle fibers with adenosine 5'-[gamma-thio]triphosphate (ATP[gamma S]) and by laser photolysis of caged ATP[gamma S]: evidence for Ca2+-dependent affinity of rapidly detaching zero-force cross-bridges.

Authors:  J A Dantzig; J W Walker; D R Trentham; Y E Goldman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

4.  New states of actomyosin.

Authors:  D Applegate; P Flicker
Journal:  J Biol Chem       Date:  1987-05-15       Impact factor: 5.157

Review 5.  Mechanical and structural approaches to correlation of cross-bridge action in muscle with actomyosin ATPase in solution.

Authors:  B Brenner
Journal:  Annu Rev Physiol       Date:  1987       Impact factor: 19.318

6.  Force generating mechanisms in striated muscle.

Authors:  R J Podolsky; T Arata
Journal:  Adv Exp Med Biol       Date:  1988       Impact factor: 2.622

7.  Proposed mechanism of force generation in striated muscle.

Authors:  A F Huxley; R M Simmons
Journal:  Nature       Date:  1971-10-22       Impact factor: 49.962

8.  Resolution of conformational states of spin-labeled myosin during steady-state ATP hydrolysis.

Authors:  V A Barnett; D D Thomas
Journal:  Biochemistry       Date:  1987-01-13       Impact factor: 3.162

9.  Effects of AMPPNP on the orientation and rotational dynamics of spin-labeled muscle cross-bridges.

Authors:  P G Fajer; E A Fajer; N J Brunsvold; D D Thomas
Journal:  Biophys J       Date:  1988-04       Impact factor: 4.033

10.  Energetics of the actomyosin bond in the filament array of muscle fibers.

Authors:  E Pate; R Cooke
Journal:  Biophys J       Date:  1988-04       Impact factor: 4.033

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  24 in total

1.  Mammalian cardiac muscle thick filaments: their periodicity and interactions with actin.

Authors:  Robert W Kensler
Journal:  Biophys J       Date:  2002-03       Impact factor: 4.033

2.  Evidence for structurally different attached states of myosin cross-bridges on actin during contraction of fish muscle.

Authors:  J J Harford; J M Squire
Journal:  Biophys J       Date:  1992-08       Impact factor: 4.033

3.  Structural dynamics of the actomyosin complex probed by a bifunctional spin label that cross-links SH1 and SH2.

Authors:  Andrew R Thompson; Nariman Naber; Clyde Wilson; Roger Cooke; David D Thomas
Journal:  Biophys J       Date:  2008-09-19       Impact factor: 4.033

4.  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

5.  Steady-state fluorescence polarization studies of the orientation of myosin regulatory light chains in single skeletal muscle fibers using pure isomers of iodoacetamidotetramethylrhodamine.

Authors:  C Sabido-David; B Brandmeier; J S Craik; J E Corrie; D R Trentham; M Irving
Journal:  Biophys J       Date:  1998-06       Impact factor: 4.033

6.  Observation of transient disorder during myosin subfragment-1 binding to actin by stopped-flow fluorescence and millisecond time resolution electron cryomicroscopy: evidence that the start of the crossbridge power stroke in muscle has variable geometry.

Authors:  M Walker; X Z Zhang; W Jiang; J Trinick; H D White
Journal:  Proc Natl Acad Sci U S A       Date:  1999-01-19       Impact factor: 11.205

7.  Orientation of intermediate nucleotide states of indane dione spin-labeled myosin heads in muscle fibers.

Authors:  O Roopnarine; D D Thomas
Journal:  Biophys J       Date:  1996-06       Impact factor: 4.033

8.  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

9.  Conformationally trapping the actin-binding cleft of myosin with a bifunctional spin label.

Authors:  Rebecca J Moen; David D Thomas; Jennifer C Klein
Journal:  J Biol Chem       Date:  2012-12-18       Impact factor: 5.157

10.  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

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