4
Views
5
CrossRef citations to date
0
Altmetric
Original Article

Properties of the Ryanodine Receptor Present in the Sarcoplasmic Reticulum from Lobster Skeletal Muscle

, &
Pages 221-235 | Received 30 Sep 1993, Accepted 06 Oct 1993, Published online: 09 Jul 2009

References

  • Airey J. A., Beck C. F., Murakami K., Tanksley S. J., Deerinck T. J., Ellisman M. H., Sutko J. L. Identification and localization of two triad junctional foot protein isoforms in mature avian fast twitch skeletal muscle. J. Biol. Chem. 1990; 65: 14187–14194
  • Arispe N., Pollard H. B., Rojas E. Calcium independent K+-selective channel from chromaffin granule membranes. J. Memb. Biol. 1992; 130: 191–202
  • Armstrong C. M., Bezanilla A. F., Horowicz P. Twitches in the presence of ethylene glycol bis(-aminoethyl ether)-N,N'-tetracetic acid. Biochim. Biophys. Acta 1972; 267: 605–608
  • Atwater I., Rojas E., Vergara J. Calcium influxes and tension development in perfused single barnacle muscle fibres under membrane potential control. J. Physiol. (Lond.) 1974; 243: 523–551
  • Campbell K. P., Knudson C. M., Imagawa T., Leung A. T., Sutko J. L., Kahl S. D., Raab C. R., Madson L. Identification and characterization of the high affinity [3H]ryanodine receptor of the junctional sarcoplasmic reticulum Ca2+ release channel. J. Biol. Chem. 1987; 262: 6460–6463
  • Chu A., Diaz-Munoz M., Hawkes M. J., Brush K., Hamilton S. L. Ryanodine as a probe for the functional state of the skeletal muscle sarcoplasmic reticulum calcium release channel. Mol. Pharm. 1990; 37: 735–741
  • Formelova J., Hurnak O., Novotova M., Zachar J. Ryanodine receptor purified from crayfish skeletal muscle. Gen. Physiol. Biophys. 1990; 9(5)445–453
  • Garcia J., Sakar A., Avila J., Stefani E. Differential effects of ryanodine and tetracaine on charge movement and calcium transients in frog skeletal muscle. J. Physiol. (Lond.) 1991; 440: 403–417
  • Hidalgo J., Luxoro M., Rojas E. On the role of extracellular calcium in triggering contraction in muscle fibres from barnacle under membrane potential control. J. Physiol. (Lond.) 1979; 288: 313–330
  • Inui M., Saito A., Fleisher S. Purification of the ryanodine receptor and identity with feet structures of junctional termianl cisternae of sarcoplasmic reticulum. J. Biol. Chem. 1987; 262: 1740–1747
  • Keynes R. D., Rojas E., Taylor R. E., Vergara J. Calcium and potassium systems of a giant barnacle muscle under membrane potential control. J. Physiol. 1973; 229: 409–455
  • Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970; 227: 680–685
  • Lai F. A., Misra M., Xu L., Smith H. A., Meissner G. The ryanodine receptor-Ca2+ release channel complex of skeletal muscle sarcoplasmic reticulum. J. Biol. Chem. 1989; 264(28)16776–16785
  • Luxoro M., Nassar-Gentina V. Potassium-induced depolarizations and generation of tension in barnacle muscle fibres: effect of external calcium, strontium and barium. Quat. J. Exp. Physiol. 1984; 69: 235–243
  • Luxoro M., Nassar-Gentina V., Rojas E. Excitation-contraction coupling in barnacle muscle-fibers: does calcium entry trigger contraction directly?. Transduction in Biological Systems, C. Hidalgo, J. Bacigalupo, E. Jaimovich, J. Vergara. Plenum. 1990; 289–300
  • Meissner G. Adenine nucleotide stimulation of Ca2+-induced Ca2+-release in sarcoplasmic reticulum. J. Biol. Chem. 1984; 259: 2365–2374
  • Meissner G. Ryanodine activation and inhibition of the Ca2+ release channel of sarcoplasmic reticulum. J. Biol. Chem. 1986; 261: 6300–6306
  • Mignery G. A., Sudhof T. C, Takei K., De Camilli P. Putative receptor for inositol 1,4,5-trisphosphate similar to ryanodine receptor. Nature 1989; 342: 192–195
  • Millman M. S., Azari J. Adenosine triphosphate-induced rapid calcium release from fragmented sarcoplasmic reticulum. Biochem. Biophys. Res. Comm. 1977; 78: 60–66
  • Mermier P., Hasselbach W. Comparison between strontium and calcium uptake by the fragmented sarcoplasmic reticulum. Eur. J. Biochem. 1976; 69: 79–86
  • Nagasaki K., Kasai M. Calcium-induced calcium release from sarcoplasmic reticulum vesicles. J. Biochem. (Tokyo) 1981; 90: 749–755
  • Ogawa Y. Some properties of fragmented frog sarcoplasmic reticulum with particular reference to its response to caffeine. J. Biochem. (Tokyo) 1970; 67: 667–683
  • Ohnishi S. T. Calcium-induced calcium release from fragmented sarcoplasmic reticulum. J. Biochem. (Tokyo) 1979; 86: 1147–1150
  • Olivares E. B., Tanksley S. J., Airey J. A., Beck C. F., Ouyang Y., Deerinck T. J., Ellisman M. H., Sutko J. L. Nonmammalian vertebrate skeletal muscles express two triad junctional foot protein isoforms. Biophys. J. 1991; 59: 1153–1163
  • Padula R. A., Wan W. H., Nagy J. I., Geiger J. D. [3H]ryanodine binding sites in rat brain demonstrated by membrane binding and autoradiography. Brain Res. 1991; 542: 135–140
  • Pessah I. N., Waterhouse A. L., Cassida J. E. The calcium-ryanodine receptor complex of skeletal and cardiac muscle. Biochem. Biophys. Res. Comm. 1985; 128: 449–456
  • Pessah I. N., Francini A. O., Scales D. J., Waterhouse A. L., Casida J. E. Calcium-ryanodine receptor complex. Solubilization and partial characterization from skeletal muscle junctional sarcoplasmic reticulum vesicles. J. Biol. Chem. 1986; 261: 8643–8648
  • Potreau D., Raymond D. Slow inward barium current and contraction on frog single muscle fibres. J. Physiol. (Lond.) 1980; 303: 91–109
  • Rios E., Brum G. Involvement of dihydropyridine receptors in excitation-contraction coupling in skeletal muscle. Nature 1987; 325: 717–720
  • Rojas E., Nassar-Gentina V., Pollard M. E., Luxoro M. Mechanisms of calcium release from terminal cisternae in crustacean muscle. Adv. Exp. Med. Biol. 1992; 311: 305–317
  • Rojas E., Nassar-Gentikna V., Luxoro M., Pollard M. E., Carrasco M. A. Inositol 1,4,5-trisphosphate-induced Ca2+ release from the sarcoplasmic reticulum and contraction in crustacean muscle. Can. J. Physiol. Pharmacol. 1987; 65: 672–680
  • Saito A., Seiler S., Chu A., Fleisher S. Preparation and morphology of sarcoplasmic reticulum terminal cisternae from rabbit skeletal muscle. J. Cell. Biol. 1984; 99: 875–885
  • Seok J. H., Xu L., Kramarcy N. R., Sealok R., Meissner G. The 30 S lobster skeletal muscle Ca2+ release channel (ryanodine receptor) has functional properties distinct from the mammalian channel proteins. J. Biol. Chem. 1992; 267: 15893–15901
  • Shoshan-Barmatz V., Pressley T. A., Highham S., Kraus-Friedmann N. Characterization of high affinity ryanodine binding sites of rat liver endoplasmic reticulum. Differences between liver and skeletal muscle. Biochem. J. 1991; 276: 41–46
  • Smith P. K., Krohn R. I., Hermanson G. T., Mallia A. K., Gartner F. H., Provenzano M. D., Fujimoto E. K., Goeke N. M., Olson B. J., Klenk D. C. Meaasurement of protein using bicinchonic acid. Ann. Biochem. 1985; 150: 76–85, Erratum. Ann. Biochem. (1987) 163:279
  • Taheshima H., Nishimura S., Matsumoto T., Ishida H., Kangawa K., Minamino N., Matsuo H., Ueda M., Hanaoka M., Hirose T., Numa S. Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor. Nature 1989; 339: 439–445
  • Valdivia H., Valdivia C., Ma J., Coronado R. Direct binding of verapamil to the ryanodine receptor channel of sarcoplasmic reticulum. Biophys. J. 1990; 58: 471–481
  • Van Winkle W. B. Calcium release from skeletal muscle sarcoplasmic reticulum: site of action of dantrolene sodium?. Science 1976; 193: 1130–1131
  • Vergara J., Caputo C. Effects of tetracaine on charge movements and calcium signals in frog skeletal muscle fibers. Proc. Natl. Acad. Sci. USA 1983; 80: 1477–1481
  • Walton P. D., Airey J. A., Sutko J. L., Beck C. F., Mignery G. A., Sudhof T. C., Deerinck T. J., Ellisman M. H. Ryanodine and inositol trisphosphate receptors coexist in avian cerebellar purkinje neurons. J. Cell Biol. 1991; 113: 1145–1157
  • Weber A. The mechanism of the action of caffeine on sarcoplasmic reticulum. J. Gen. Physiol. 1968; 52: 760–772
  • Zorzato F., Fujii F., Otsu K., Phillips M., Green N., Lai F., Meissner G., McLennan D. H. Molecular cloning of cDNA encoding human and rabbit forms of the Ca2+ release channel (ryanodine receptor) of skeletal muscle sarcoplasmic reticulum. J. Biol. Chem. 1990; 265(4)2244–2256

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.