Skip to main content
Biophysical Journal logoLink to Biophysical Journal
. 1995 Nov;69(5):1847–1857. doi: 10.1016/S0006-3495(95)80055-X

Trypsin increases availability and open probability of cardiac L-type Ca2+ channels without affecting inactivation induced by Ca2+.

R Schmid 1, K Seydl 1, W Baumgartner 1, K Groschner 1, C Romanin 1
PMCID: PMC1236418  PMID: 8580328

Abstract

The patch-clamp technique was employed to investigate the response of single L-type Ca2+ channels to the protease trypsin applied to the intracellular face of excised membrane patches from guinea pig ventricular myocytes. Calpastatin and ATP were used to prevent run-down of Ca2+ channel activity monitored with 96 mM Ba2+ as charge carrier in the presence of 2.5 microM (-)-BAYK 8644. Upon application of trypsin (100 micrograms/ml) channel activity was enhanced fourfold and remained elevated upon removal of trypsin, as expected of a proteolytic, irreversible modification. The trypsin effect was not mediated by a proteolytic activation of protein kinases, as evidenced by the insensitivity of this effect to protein kinase inhibitors. Trypsin-modified Ca2+ channels exhibited the usual run-down phanomenon upon removal of calpastatin and ATP. In ensemble average currents trypsin-induced changes of channel function are apparent as a threefold increase in peak current and a reduction in current inactivation. At the single channel level these effects were based on about a twofold increase in both Ca2+ channels' availability and open probability. Neither the actual number of channels in the patch nor their unitary conductance as well as reversal potential was changed by trypsin. The Ca(2+)-induced inactivation was not impaired, as judged by a comparable sensitivity of trypsin-modified Ca2+ channels to intracellular Ca2+. Similarly, trypsin treatment did not affect the sensitivity of Ca2+ channels to phenylalkylmine inhibition. The observed alterations in channel function are discussed in terms of possible structural correlates.

Full text

PDF
1847

Selected References

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

  1. Armstrong C. M., Bezanilla F., Rojas E. Destruction of sodium conductance inactivation in squid axons perfused with pronase. J Gen Physiol. 1973 Oct;62(4):375–391. doi: 10.1085/jgp.62.4.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Babitch J. Channel hands. Nature. 1990 Jul 26;346(6282):321–322. doi: 10.1038/346321b0. [DOI] [PubMed] [Google Scholar]
  3. Biel M., Ruth P., Bosse E., Hullin R., Stühmer W., Flockerzi V., Hofmann F. Primary structure and functional expression of a high voltage activated calcium channel from rabbit lung. FEBS Lett. 1990 Sep 3;269(2):409–412. doi: 10.1016/0014-5793(90)81205-3. [DOI] [PubMed] [Google Scholar]
  4. Carbone E., Swandulla D. Neuronal calcium channels: kinetics, blockade and modulation. Prog Biophys Mol Biol. 1989;54(1):31–58. doi: 10.1016/0079-6107(89)90008-4. [DOI] [PubMed] [Google Scholar]
  5. Catterall W. A., Striessnig J. Receptor sites for Ca2+ channel antagonists. Trends Pharmacol Sci. 1992 Jun;13(6):256–262. doi: 10.1016/0165-6147(92)90079-l. [DOI] [PubMed] [Google Scholar]
  6. Cavalié A., Ochi R., Pelzer D., Trautwein W. Elementary currents through Ca2+ channels in guinea pig myocytes. Pflugers Arch. 1983 Sep;398(4):284–297. doi: 10.1007/BF00657238. [DOI] [PubMed] [Google Scholar]
  7. Cavalié A., Pelzer D., Trautwein W. Fast and slow gating behaviour of single calcium channels in cardiac cells. Relation to activation and inactivation of calcium-channel current. Pflugers Arch. 1986 Mar;406(3):241–258. doi: 10.1007/BF00640910. [DOI] [PubMed] [Google Scholar]
  8. DeFelice L. J. Molecular and biophysical view of the Ca channel: a hypothesis regarding oligomeric structure, channel clustering, and macroscopic current. J Membr Biol. 1993 May;133(3):191–202. doi: 10.1007/BF00232019. [DOI] [PubMed] [Google Scholar]
  9. Eckert R., Chad J. E. Inactivation of Ca channels. Prog Biophys Mol Biol. 1984;44(3):215–267. doi: 10.1016/0079-6107(84)90009-9. [DOI] [PubMed] [Google Scholar]
  10. Giannattasio B., Jones S. W., Scarpa A. Calcium currents in the A7r5 smooth muscle-derived cell line. Calcium-dependent and voltage-dependent inactivation. J Gen Physiol. 1991 Nov;98(5):987–1003. doi: 10.1085/jgp.98.5.987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Haack J. A., Rosenberg R. L. Calcium-dependent inactivation of L-type calcium channels in planar lipid bilayers. Biophys J. 1994 Apr;66(4):1051–1060. doi: 10.1016/S0006-3495(94)80886-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hadley R. W., Hume J. R. An intrinsic potential-dependent inactivation mechanism associated with calcium channels in guinea-pig myocytes. J Physiol. 1987 Aug;389:205–222. doi: 10.1113/jphysiol.1987.sp016654. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hadley R. W., Lederer W. J. Ca2+ and voltage inactivate Ca2+ channels in guinea-pig ventricular myocytes through independent mechanisms. J Physiol. 1991 Dec;444:257–268. doi: 10.1113/jphysiol.1991.sp018876. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Hamill O. P., Marty A., Neher E., Sakmann B., Sigworth F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pflugers Arch. 1981 Aug;391(2):85–100. doi: 10.1007/BF00656997. [DOI] [PubMed] [Google Scholar]
  15. Hescheler J., Trautwein W. Modification of L-type calcium current by intracellularly applied trypsin in guinea-pig ventricular myocytes. J Physiol. 1988 Oct;404:259–274. doi: 10.1113/jphysiol.1988.sp017289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Hess P., Lansman J. B., Tsien R. W. Calcium channel selectivity for divalent and monovalent cations. Voltage and concentration dependence of single channel current in ventricular heart cells. J Gen Physiol. 1986 Sep;88(3):293–319. doi: 10.1085/jgp.88.3.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hirano Y., Suzuki K., Yamawake N., Hiraoka M. Multiple kinetic effects of beta-adrenergic stimulation on single cardiac L-type Ca channels. Am J Physiol. 1994 Jun;266(6 Pt 1):C1714–C1721. doi: 10.1152/ajpcell.1994.266.6.C1714. [DOI] [PubMed] [Google Scholar]
  18. Hofmann F., Biel M., Flockerzi V. Molecular basis for Ca2+ channel diversity. Annu Rev Neurosci. 1994;17:399–418. doi: 10.1146/annurev.ne.17.030194.002151. [DOI] [PubMed] [Google Scholar]
  19. Horn R. Estimating the number of channels in patch recordings. Biophys J. 1991 Aug;60(2):433–439. doi: 10.1016/S0006-3495(91)82069-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Inagaki M., Kawamoto S., Hidaka H. Serotonin secretion from human platelets may be modified by Ca2+-activated, phospholipid-dependent myosin phosphorylation. J Biol Chem. 1984 Dec 10;259(23):14321–14323. [PubMed] [Google Scholar]
  21. Isom L. L., De Jongh K. S., Catterall W. A. Auxiliary subunits of voltage-gated ion channels. Neuron. 1994 Jun;12(6):1183–1194. doi: 10.1016/0896-6273(94)90436-7. [DOI] [PubMed] [Google Scholar]
  22. Kawamoto S., Hidaka H. 1-(5-Isoquinolinesulfonyl)-2-methylpiperazine (H-7) is a selective inhibitor of protein kinase C in rabbit platelets. Biochem Biophys Res Commun. 1984 Nov 30;125(1):258–264. doi: 10.1016/s0006-291x(84)80362-9. [DOI] [PubMed] [Google Scholar]
  23. Klöckner U., Isenberg G. Intracellular pH modulates the availability of vascular L-type Ca2+ channels. J Gen Physiol. 1994 Apr;103(4):647–663. doi: 10.1085/jgp.103.4.647. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Koch W. J., Ellinor P. T., Schwartz A. cDNA cloning of a dihydropyridine-sensitive calcium channel from rat aorta. Evidence for the existence of alternatively spliced forms. J Biol Chem. 1990 Oct 15;265(29):17786–17791. [PubMed] [Google Scholar]
  25. Mazzanti M., DeFelice L. J., Liu Y. M. Gating of L-type Ca2+ channels in embryonic chick ventricle cells: dependence on voltage, current and channel density. J Physiol. 1991 Nov;443:307–334. doi: 10.1113/jphysiol.1991.sp018835. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. McDonald T. F., Pelzer S., Trautwein W., Pelzer D. J. Regulation and modulation of calcium channels in cardiac, skeletal, and smooth muscle cells. Physiol Rev. 1994 Apr;74(2):365–507. doi: 10.1152/physrev.1994.74.2.365. [DOI] [PubMed] [Google Scholar]
  27. Neely A., Olcese R., Wei X., Birnbaumer L., Stefani E. Ca(2+)-dependent inactivation of a cloned cardiac Ca2+ channel alpha 1 subunit (alpha 1C) expressed in Xenopus oocytes. Biophys J. 1994 Jun;66(6):1895–1903. doi: 10.1016/S0006-3495(94)80983-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Obejero-Paz C. A., Jones S. W., Scarpa A. Calcium currents in the A7r5 smooth muscle-derived cell line. Increase in current and selective removal of voltage-dependent inactivation by intracellular trypsin. J Gen Physiol. 1991 Dec;98(6):1127–1140. doi: 10.1085/jgp.98.6.1127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Ochi R., Kawashima Y. Modulation of slow gating process of calcium channels by isoprenaline in guinea-pig ventricular cells. J Physiol. 1990 May;424:187–204. doi: 10.1113/jphysiol.1990.sp018062. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Romanin C., Grösswagen P., Schindler H. Calpastatin and nucleotides stabilize cardiac calcium channel activity in excised patches. Pflugers Arch. 1991 Mar;418(1-2):86–92. doi: 10.1007/BF00370456. [DOI] [PubMed] [Google Scholar]
  31. Romanin C., Karlsson J. O., Schindler H. Activity of cardiac L-type Ca2+ channels is sensitive to cytoplasmic calcium. Pflugers Arch. 1992 Aug;421(5):516–518. doi: 10.1007/BF00370266. [DOI] [PubMed] [Google Scholar]
  32. Seydl K., Karlsson J. O., Dominik A., Gruber H., Romanin C. Action of calpastatin in prevention of cardiac L-type Ca2+ channel run-down cannot be mimicked by synthetic calpain inhibitors. Pflugers Arch. 1995 Feb;429(4):503–510. doi: 10.1007/BF00704155. [DOI] [PubMed] [Google Scholar]
  33. Tanabe T., Takeshima H., Mikami A., Flockerzi V., Takahashi H., Kangawa K., Kojima M., Matsuo H., Hirose T., Numa S. Primary structure of the receptor for calcium channel blockers from skeletal muscle. Nature. 1987 Jul 23;328(6128):313–318. doi: 10.1038/328313a0. [DOI] [PubMed] [Google Scholar]
  34. Tokumitsu H., Chijiwa T., Hagiwara M., Mizutani A., Terasawa M., Hidaka H. KN-62, 1-[N,O-bis(5-isoquinolinesulfonyl)-N-methyl-L-tyrosyl]-4-phenylpiperazi ne, a specific inhibitor of Ca2+/calmodulin-dependent protein kinase II. J Biol Chem. 1990 Mar 15;265(8):4315–4320. [PubMed] [Google Scholar]
  35. Varadi G., Mori Y., Mikala G., Schwartz A. Molecular determinants of Ca2+ channel function and drug action. Trends Pharmacol Sci. 1995 Feb;16(2):43–49. doi: 10.1016/s0165-6147(00)88977-4. [DOI] [PubMed] [Google Scholar]
  36. Wei X., Neely A., Lacerda A. E., Olcese R., Stefani E., Perez-Reyes E., Birnbaumer L. Modification of Ca2+ channel activity by deletions at the carboxyl terminus of the cardiac alpha 1 subunit. J Biol Chem. 1994 Jan 21;269(3):1635–1640. [PubMed] [Google Scholar]
  37. Yue D. T., Backx P. H., Imredy J. P. Calcium-sensitive inactivation in the gating of single calcium channels. Science. 1990 Dec 21;250(4988):1735–1738. doi: 10.1126/science.2176745. [DOI] [PubMed] [Google Scholar]
  38. Yue D. T., Herzig S., Marban E. Beta-adrenergic stimulation of calcium channels occurs by potentiation of high-activity gating modes. Proc Natl Acad Sci U S A. 1990 Jan;87(2):753–757. doi: 10.1073/pnas.87.2.753. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Zong S., Zhou J., Tanabe T. Molecular determinants of calcium-dependent inactivation in cardiac L-type calcium channels. Biochem Biophys Res Commun. 1994 Jun 30;201(3):1117–1123. doi: 10.1006/bbrc.1994.1821. [DOI] [PubMed] [Google Scholar]

Articles from Biophysical Journal are provided here courtesy of The Biophysical Society

RESOURCES