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Bioscience, Biotechnology, and Biochemistry Volume 68, 2004 - Issue 1
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Original Articles

Anisodamine Causes the Changes of Structure and Function in the Transmembrane Domain of the Ca2+-ATPase from Sarcoplasmic Reticulum

Yu-Hong PANGNational Laboratory of Biomacromolecules, Institute of Biophysics, Academia Sinica
&
Jian-Wen CHENNational Laboratory of Biomacromolecules, Institute of Biophysics, Academia Sinica
Pages 126-131 | Received 16 Jul 2003, Accepted 22 Sep 2003, Published online: 22 May 2014

  • 1) Xie, J. X., Liu, C. X., Jia, X. X., and Zhou, J., The total synthesis of anisodamine. Chin. Sci. Bull., 20, 197–198 (1975).
  • 2) Hwang, F., Wang, S. M., and Hu, C. C., The disordering effect of hyoscyamine drugs on phospholipid membranes. Biochim. Biophys. Acta, 736, 220–225 (1983).
  • 3) Hwang, F., Wu, Y. W., and Wen, D. C., Anisodamine induces the hexagonal phase in phospholipid liposomes. Biochim. Biophys. Acta, 860, 713–716 (1986).
  • 4) Chen, J. W., Liu, F. S., and Hwang, F., Effects of anisodamine on the phase behavior of DPPG/DMPC binary mixtures. Chemistry and Physics of lipid, 91, 119–127 (1998).
  • 5) Hao, Y. H., Xu, Y. M., Chen, J. W., and Hwang, F., A drug-lipid interaction model: atropine induces interdigitated bilayer structure. Biochem. Biophys. Res. Commun., 245, 439–442 (1998).
  • 6) Wang, P. Y., Chen, J. W., and Hwang, F., Anisodamine causes acyl chain interdigitation in phosphatidylglycerol. FEBS Lett., 332, 193–196 (1993).
  • 7) Xie, J. P., and Hwang, F., The effect of anisodamine on the activity and transport function of Ca2+-ATPase of sarcoplasmic reticulum. Acta Biophys. Sinica., 3, 387–393 (1987).
  • 8) Wang, P. Y., Chen, J. W., and Hwang, F., Effect of anisodamine on conformation and activity of rabbit kidney (Na2+-K+)-ATPase through interaction with membrane. Acta Biophys. Sinica., 8, 216–220 (1992).
  • 9) He, J. P., and Wang, S. M., Interaction of anisodamine with acid phospholipid. Acta Biophys. Sinica., 4, 7–11 (1988).
  • 10) Clarke, D. M., Loo, T. W., Inesi, G., and Maclennan, D. H., Location of high affinity Ca2+-binding sites within the predicted transmembrane domain of the sarcoplasmic reticulum Ca2+-ATPase. Nature, 339, 476–478 (1989).
  • 11) Lepock, J. R., Rodahl, A. M., Zhang, C., Heynen, M. L., Waters, B., and Cheng, K. H., Thermal denaturation of the Ca2+-ATPase of sarcoplasmic reticulum reveals two thermodynamically independent domains. Biochemistry, 29, 681–689 (1990).
  • 12) Michelangeli, F., and Munkonge, F. M., Methods of reconstitution of the purified sarcoplasmic reticulum (Ca2+-Mg2+)-ATPase using bile salt detergents to form memberanes of defined lipid to protein ratios sealed vesicles. Anal. Biochem., 194, 231–236 (1991).
  • 13) Peterson, G. L., A simplification of the protein assay method of Lowry et al. Which is more generally applicable. Anal. Biochem., 83, 346–356 (1977).
  • 14) Fabiato, A., and Fabiato, F., Effects of pH on the myofilaments and the sarcoplasmic reticulum of skinned cells from cardiac and skeleted muscles. J. Physiol., 276, 233–255 (1978).
  • 15) Stryer, L., The interaction of a naphthalene dye with apomyoglobin and apohemoglobin. A fluorescent probe of non-polar binding sites. J. Mol. Biol., 13, 482–495 (1965).
  • 16) Michelangeli, F., Colyer, J., East, J. M., and Lee, A. G., Effect of pH on the activity of the Ca2++Mg2+-activated ATPase of sarcoplasmic reticulum. Biochem. J., 267, 423–429 (1990).
  • 17) Gould, G. W., Mcwhirter, J. M., and Lee, A. G., A fast passive Ca2+-efflux mediated by the (Ca2++Mg2+)-ATPase in reconstituted vesicles. Biochim. Biophys. Acta, 904, 45–54 (1987).
  • 18) Senisterra, G. A., and Lepock, J. R., Thermal destabilization of transmembrane proteins by local anaesthetics. Int. J. Hyperthermia, 16, 1–17 (2000).
  • 19) Gutierrez-Merino, C., Molina, A., Escudero, B., Diez, A., and Laynez, J., Interaction of the local anaesthetics dibucaine and tetracaine with sarcoplasmic reticulum membrane. Differentical scanning calorimetry and fluorescence studies. Biochemistry, 28, 3398–3406 (1989).
  • 20) Anteneodo, C., Rodahl, A. M., Meiering, E., Heynen, M. L., Sennisterra, G. A., and Lepock, J. R., Interaction of dibucaine with the transmembrane domain of Ca2+-ATPase of sarcoplasmic reticulum. Biochemistry, 33, 12283–12290 (1994).
  • 21) Fan, Y. X., Zhou, J. M., Kihara, H., and Tsou, C. L., Unfolding and refolding of dimeric creatine kinase: equilibrium and kinetic studies. Protein Science, 7, 2631–2641 (1998).
  • 22) Maclennan, D. H., Molecular tools to elucidate problems in excitation-contraction coupling. Biophys. J., 58, 1355–1366 (1990).
  • 23) Wang, Y. L., Tsui, Z. C., and Yang, F. Y., Antagonistic effect of ganglioside GM1 and GM3 on the activity and conformation of sarcoplasmic reticulum Ca2+-ATPase. FEBS Lett., 457, 144–148 (1999).

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