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Seasonal changes in the activation of crossbridge motions of isolated thick filament from Limulus striated muscle

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Summary

In dynamic light scattering, measurements of the intensity-intensity time correlation function from a suspension of rod-like particles of length L could reveal dynamical information related to translational and internal motions of those particles. For a suspension of thick filaments isolated from the myosin-regulated, striated muscles of Limulus at KL>1 (where K is the scattering vector), the average characteristic linewidth (\(\bar \Gamma\)) increased with the addition of Ca2+ or with the depletion of ATP. The increase in the \(\bar \Gamma\) with the addition of Ca2+ could be due to the presence of energy-requiring, high-frequency motions of the crossbridges activated by Ca2+. The increase in \(\bar \Gamma\) which occurred with the depletion of ATP was assumed to be mainly due to the thermal motions of the crossbridges after they had moved radially away from the filament backbone. The percentage increase in \(\bar \Gamma\) following the addition of Ca2+ was found to be seasonal, i.e., values of \(\bar \Gamma\) obtained from thick filaments isolated between the middle of June and the middle of September were smaller than those obtained during the rest of the year. The effect of temperature on the percentage increase in \(\bar \Gamma\) was also different. The increase showed a maximum at about 35°C during the summer and at about 25°C at other times. However, the percentage increase in \(\bar \Gamma\) developed under ATP-depleted conditions showed no temperature-related maximum. The number of bound Ca2+ per myosin molecule was 1 during the summer and 2 at other times.

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Abbreviations

DLS:

dynamic light scattering

L:

length

K:

scattering vector

SDS-PAGE:

sodium dodecyl sulfate polyacrylamide gel electrophoresis

\(\bar \Gamma\) :

average characteristic line width

References

  • Capputo C, Gimenez M (1967) Effect of external calcium deprivation on single muscle fiber. J Gen Physiol 50:2177–2195

    Google Scholar 

  • Chantler PD, Szent-Györgyi AG (1980) Regulatory light-chain and scallop myosin: full dissociation, reversibility and co-operative effects. J Mol Biol 138:473–492

    Google Scholar 

  • Chu B, Shih-fang Fan, Dewey MM, Gaylinn B, Greguski RR (1984) Laser light scattering studies of active and passive cross-bridge motions of muscle filaments in suspension (abstract). Biophys J 45:253a

  • Fan Shih-fang, Wen YS (1979) Concerning the binding sites of myofibril with Congo red-stained glycerinated sartorious muscle fiber. Acta Physiol Sinica 31:227–238

    Google Scholar 

  • Fan Shih-fang, Dewey MM, Colflesh D, Chu B, Kubota K (1983a) Active cross-bridge motions in Limulus thick myofilaments as revealed by quasi-elastic light-scattering studies (abstract). Biophys J 41:261a

  • Fan Shih-fang, Dewey MM, Colflesh D, Chu B (1983b) Further evidence of cross-bridge motions in Limulus thick myofilament suspensions. In: Earnshaw JC, Steer MW (eds) The application of laser light scattering to the study of biological motion. Plenum Press, New York, pp 477–483

    Google Scholar 

  • Fan Shih-fang, Dewey MM, Colflesh D, Brink P, Chu B (1984) Dynamic laser light scattering of papain-treated thick filaments from Limulus striated muscle in suspension. In: Pollack GF, Sugi H (eds) Contractile mechanisms in muscle. Plenum Press, New York, pp 88–92

    Google Scholar 

  • Fan Shih-fang, Dewey MM, Colflesh D, Gaylinn B, Greguski R, Chu B (1985a) The active cross-bridge motions of isolated thick filaments from myosin-regulated muscles detected by quasi-elastic light scattering. Biophys J 47:809–821

    Google Scholar 

  • Fan Shih-fang, Dewey MM, Colflesh D (1985b) Radial movement of cross-bridges of isolated thick filaments in ATP-free media (abstract). Biophys J 47:468a

    Google Scholar 

  • Fan Shih-fang, Dewey MM, Colflesh D, Gaylinn B, Greguski R, Chu B (1985c) Suppression of active cross-bridge motions of isolated thick myofilaments in suspension by phenylmethylsulfonyl fluoride. Biochim Biophys Acta 827:101–105

    Google Scholar 

  • Fan Shih-fang, Dewey MM, Colflesh D, Chu B (1987) Effects of ATP depletion on the isolated thick filament of Limulus striated muscle. Biophys J 52:859–866

    Google Scholar 

  • Fan Shih-fang, Dewey MM, Chu B (1988) The effect of temperature on different modes of crossbridge motions in isolated thick filaments from Limulus striated muscle as detected by quasi-elastic light scattering methods (abstract). Biophys J 53:369a

  • Gaylinn B, Dewey MM (1986) Paramyosin and myosin content of the thick filament in the striated muscle of Limulus. J Muscle Res Cell Mot 7:467–473

    Google Scholar 

  • Hoyle G, Wiersma CAG (1958) Excitation at neuromuscular junctions in crustacea. J Physiol (Lond) 143:403–425

    Google Scholar 

  • Huxley HE (1972) Structural changes in the actin- and myosin-containing filaments during contraction. Cold Spring Harbor Symp Quant Biol 37:1336–1376

    Google Scholar 

  • Jenerick HP, Gerard RW (1953) Membrane potential and threshold of single muscle fiber. J Cell Comp Physiol 42:79–102

    Google Scholar 

  • Kendrick-Jones J, Lehman W, Szent-Györgyi AG (1970) Regulation in molluscan muscle. J Mol Biol 54:313–326

    Google Scholar 

  • Koppel DR (1972) Analysis of macromolecular polydispersity in intensity correlation spectroscopy. The method of cumulants. J Chem Phys 57:4814–4820

    Google Scholar 

  • Kubota K, Chu B, Fan Shih-fang, Dewey MM, Brink P, Colflesh D (1983) Quasi-elastic light scattering of suspensions of Limulus thick myofilaments in relaxed (long), activated and rerelaxed (short) state. J Mol Biol 166:329–340

    Google Scholar 

  • Lehman W, Szent-Györgyi AG (1975) Regulation of muscular contraction. Distribution of actin control and myosin control in the animal kingdom. J Gen Physiol 66:1–30

    Google Scholar 

  • Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–282

    Google Scholar 

  • Maeda T, Fujime S (1981) Effect of filament flexibility on the dynamic light-scattering spectrum with special reference to fd virus and muscle thin filaments. Macromolecules 14:809–818

    Google Scholar 

  • Newman JH, Carlson FD (1980) Dynamic light-scattering evidence for the flexibility of native muscle thin filaments. Biophys J 29:37–48

    Google Scholar 

  • Perrin DD, Sayce IG (1967) Computer calculation of equilibrium concentrations in mixtures of metal ions and complexing species. Talanta 14:833–842

    Google Scholar 

  • Strickholm A (1966) Local sarcomere contraction in fast muscle fibers (Rana spp.). Nature 212:835–836

    Google Scholar 

  • Strickholm A (1974) Intracellular generated potential during excitation contraction coupling in muscle. J Neurobiol 51:161–187

    Google Scholar 

  • Suzuki N, Wada A (1981) Quasielastic light scattering study of solutions of synthetic myosin filaments. Biochim Biophys Acta 670:308–420

    Google Scholar 

  • Szent-Györgyi AG, Szentkirályi DM (1973) The light chains of scallop myosin as regulatory subunits. J Mol Biol 74:179–203

    Google Scholar 

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Fan, Sf., Dewey, M.M., Gaylinn, B. et al. Seasonal changes in the activation of crossbridge motions of isolated thick filament from Limulus striated muscle. J Comp Physiol B 162, 508–512 (1992). https://doi.org/10.1007/BF00264810

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  • DOI: https://doi.org/10.1007/BF00264810

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