Literature DB >> 1755357

Two-dimensional time resolved X-ray diffraction of muscle: recent results.

J Bordas1, G P Diakun, J E Harries, R A Lewis, G R Mant, M L Martin-Fernandez, E Towns-Andrews.   

Abstract

This report provides a preliminary sketch of the results obtained in a two-dimensional time resolved X-ray diffraction study of "live" frog sartorius muscles undergoing isometric tetani. These results demonstrate the recently developed capability to record time resolved (10 msec time resolution), two-dimensional X-ray diffraction diagrams throughout the cycle of contraction. The correlation between the time courses of the diffraction features in the whole of the diffraction diagram establishes a sequence of structural events, which suggest that during the transition from rest to the plateau of tension and the subsequent recovery, the following sequence of events takes place: a) Following the activation phase, which is best monitored by the increase of intensity on the second actin layer line at 18.0 nm spacing (5), there is the onset of three dimensional disorder due to the filaments losing their axial alignment and the myosin heads rotating azimuthally and moving radially outwards. A set of low-angle layer lines, following the actin based spacings seen in rigor (i.e., at spacings of ca. 36.5-37.5, 24.0 and 18.0 nm) become visible and those at ca. 24.0 and 18.0 nm appear to increase in intensity during this phase with a time course that cannot be determined accurately because of the proximity of the neighbouring first, second and third myosin layer lines and the weakness of these diffraction features. Whether the first of these layer lines increases or not is difficult to ascertain. Moreover, proper account of the loss in crystallinity during the development of tension must be made before the comparisons in intensity between the rest and peak of tension states have any significance. Nevertheless, these features together with the behaviour of the equatorial reflections and the meridional region of the third myosin layer line indicate that a sizeable fraction of the crossbridges may become axially disposed with an actin based periodicity. The formation of this complex does not immediately result in the generation of tension. The labelling of the thin filaments is also reflected in the main actin layer lines at 5.9 and 5.1 nm. b) The tension generating phase is monitored by the intensity changes in the meridional region of the third myosin layer line, which are best explained by a change in the orientation/conformation of the tension bearing crossbridges, (which probably adopt a more perpendicular orientation to the filament axis). c) At the end of stimulation, the crossbridges return to an axial spacing and axial orientation (although not yet azimuthal) similar to the one at rest.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1755357     DOI: 10.1016/0065-227x(91)90005-x

Source DB:  PubMed          Journal:  Adv Biophys        ISSN: 0065-227X


  8 in total

1.  Structural changes in the actin-myosin cross-bridges associated with force generation induced by temperature jump in permeabilized frog muscle fibers.

Authors:  A K Tsaturyan; S Y Bershitsky; R Burns; M A Ferenczi
Journal:  Biophys J       Date:  1999-07       Impact factor: 4.033

2.  Direct x-ray observation of a single hexagonal myofilament lattice in native myofibrils of striated muscle.

Authors:  Hiroyuki Iwamoto; Yukihiro Nishikawa; Jun'ichi Wakayama; Tetsuro Fujisawa
Journal:  Biophys J       Date:  2002-08       Impact factor: 4.033

3.  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

4.  Structure and periodicities of cross-bridges in relaxation, in rigor, and during contractions initiated by photolysis of caged Ca2+.

Authors:  T D Lenart; J M Murray; C Franzini-Armstrong; Y E Goldman
Journal:  Biophys J       Date:  1996-11       Impact factor: 4.033

5.  Mechanical and structural properties underlying contraction of skeletal muscle fibers after partial 1-ethyl-3-[3-dimethylamino)propyl]carbodiimide cross-linking.

Authors:  S Bershitsky; A Tsaturyan; O Bershitskaya; G Mashanov; P Brown; M Webb; M A Ferenczi
Journal:  Biophys J       Date:  1996-09       Impact factor: 4.033

6.  Time-resolved X-ray diffraction studies of myosin head movements in live frog sartorius muscle during isometric and isotonic contractions.

Authors:  M L Martin-Fernandez; J Bordas; G Diakun; J Harries; J Lowy; G R Mant; A Svensson; E Towns-Andrews
Journal:  J Muscle Res Cell Motil       Date:  1994-06       Impact factor: 2.698

7.  Flash and smash: rapid freezing of muscle fibers activated by photolysis of caged ATP.

Authors:  K Hirose; T D Lenart; J M Murray; C Franzini-Armstrong; Y E Goldman
Journal:  Biophys J       Date:  1993-07       Impact factor: 4.033

8.  Two-dimensional time-resolved X-ray diffraction studies of live isometrically contracting frog sartorius muscle.

Authors:  J Bordas; G P Diakun; F G Diaz; J E Harries; R A Lewis; J Lowy; G R Mant; M L Martin-Fernandez; E Towns-Andrews
Journal:  J Muscle Res Cell Motil       Date:  1993-06       Impact factor: 2.698

  8 in total

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