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. 1981 Jan;33(1):39–62. doi: 10.1016/S0006-3495(81)84871-0

Quasi-elastic light-scattering studies of single skeletal muscle fibers.

R C Haskell, F D Carlson
PMCID: PMC1327396  PMID: 6974014

Abstract

Measurements were made of the intensity autocorrelation function, g(2)[tau], of light scattered from intact frog muscle fibers. During the tension plateau of an isometric tenanus, scattered field statistics were approximately Gaussian and intensity fluctuations were quasi-stationary. The half time, tau 1/2, for the decay of g(2)[tau] was typically 70 ms at a scattering angle of 30 degrees. The decay rate, 1/tau 1/2, of g(2)[tau] varied roughly linearly with the projection of the scattering vector on the fiber axis. 1/tau 1/2 was greater during the tension creep phase of tetani of highly stretched fibers, but was roughly independent of sarcomere length during the tension plateau. g(2)[tau] measured during rest or on diffraction pattern maxima during isometric contraction were flat with low amplitudes. These results are consistent with a model of a 200-mu m segment of an isometrically contracting fiber in which scattering material possesses relative axial velocities of 1-2 mu m/s accompanied by relative axial displacements greater than 0.1 mu m. The slow (1-2 mu m/s) motion of one portion of the fiber relative to another observed under the microscope (500X) during isometric contraction is consistent with the light-scattering results. Structural fluctuations on the scale of the myofibrillar sarcomere which may arise from asynchronous cycling of cross-bridges must involve relative axial velocities less than 3 mu m/s or relative axial displacements less than 0.05 mu m.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bonner R. F., Carlson F. D. Structural dynamics of frog muscle during isometric contraction. J Gen Physiol. 1975 May;65(5):555–581. doi: 10.1085/jgp.65.5.555. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Borejdo J., Morales M. F. Fluctuations in tension during contraction of single muscle fibers. Biophys J. 1977 Dec;20(3):315–334. doi: 10.1016/S0006-3495(77)85552-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Borejdo J., Putnam S., Morales M. F. Fluctuations in polarized fluorescence: evidence that muscle cross bridges rotate repetitively during contraction. Proc Natl Acad Sci U S A. 1979 Dec;76(12):6346–6350. doi: 10.1073/pnas.76.12.6346. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Carlson F. D., Fraser A. B. Dynamics of F-actin and F-actin complexes. J Mol Biol. 1974 Oct 25;89(2):273–281. doi: 10.1016/0022-2836(74)90518-x. [DOI] [PubMed] [Google Scholar]
  5. Carlson F. D. Letters to the editor: Kinetics. J Mol Biol. 1975 Jun 15;95(1):139–139. doi: 10.1016/0022-2836(75)90341-1. [DOI] [PubMed] [Google Scholar]
  6. Carlson F. D. Structural fluctuations in the steady state of muscular contraction. Biophys J. 1975 Jul;15(7):633–649. doi: 10.1016/S0006-3495(75)85845-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cummins H. Z., Carlson F. D., Herbert T. J., Woods G. Translational and rotational diffusion constants of tobacco mosaic virus from Rayleigh linewidths. Biophys J. 1969 Apr;9(4):518–546. doi: 10.1016/S0006-3495(69)86402-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Elliott G. F., Lowy J., Millman B. M. Low-angle x-ray diffraction studies of living striated muscle during contraction. J Mol Biol. 1967 Apr 14;25(1):31–45. doi: 10.1016/0022-2836(67)90277-x. [DOI] [PubMed] [Google Scholar]
  9. Ford L. E., Huxley A. F., Simmons R. M. Tension responses to sudden length change in stimulated frog muscle fibres near slack length. J Physiol. 1977 Jul;269(2):441–515. doi: 10.1113/jphysiol.1977.sp011911. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gordon A. M., Huxley A. F., Julian F. J. Tension development in highly stretched vertebrate muscle fibres. J Physiol. 1966 May;184(1):143–169. doi: 10.1113/jphysiol.1966.sp007908. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gordon A. M., Huxley A. F., Julian F. J. The variation in isometric tension with sarcomere length in vertebrate muscle fibres. J Physiol. 1966 May;184(1):170–192. doi: 10.1113/jphysiol.1966.sp007909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. HANSON J., HUXLEY H. E. Quantitative studies on the structure of cross-striated myofibrils. II. Investigations by biochemical techniques. Biochim Biophys Acta. 1957 Feb;23(2):250–260. doi: 10.1016/0006-3002(57)90326-8. [DOI] [PubMed] [Google Scholar]
  13. HUXLEY A. F. Muscle structure and theories of contraction. Prog Biophys Biophys Chem. 1957;7:255–318. [PubMed] [Google Scholar]
  14. HUXLEY A. F., NIEDERGERKE R. Structural changes in muscle during contraction; interference microscopy of living muscle fibres. Nature. 1954 May 22;173(4412):971–973. doi: 10.1038/173971a0. [DOI] [PubMed] [Google Scholar]
  15. HUXLEY H. E., HANSON J. Quantitative studies on the structure of cross-striated myofibrils. I. Investigations by interference microscopy. Biochim Biophys Acta. 1957 Feb;23(2):229–249. doi: 10.1016/0006-3002(57)90325-6. [DOI] [PubMed] [Google Scholar]
  16. HUXLEY H., HANSON J. Changes in the cross-striations of muscle during contraction and stretch and their structural interpretation. Nature. 1954 May 22;173(4412):973–976. doi: 10.1038/173973a0. [DOI] [PubMed] [Google Scholar]
  17. Huxley H. E., Brown W. The low-angle x-ray diagram of vertebrate striated muscle and its behaviour during contraction and rigor. J Mol Biol. 1967 Dec 14;30(2):383–434. doi: 10.1016/s0022-2836(67)80046-9. [DOI] [PubMed] [Google Scholar]

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