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. 1989 Mar 1;93(3):385–410. doi: 10.1085/jgp.93.3.385

Single channel characteristics of a high conductance anion channel in "sarcoballs"

PMCID: PMC2216217  PMID: 2467963

Abstract

Previously undescribed high conductance single anion channels from frog skeletal muscle sarcoplasmic reticulum (SR) were studied in native membrane using the "sarcoball" technique (Stein and Palade, 1988). Excised inside-out patches recorded in symmetrical 200 mM TrisCl show the conductance of the channel's predominant state was 505 +/- 25 pS (n = 35). From reversal potentials, the Pcl/PK ratio was 45. The slope conductance vs. Cl- ion concentration curve saturates at 617 pS, with K0.5 estimated at 77 mM. The steady-state open probability (Po) vs. holding potential relationship produces a bell-shaped curve, with Po values reaching a maximum near 1.0 at 0 mV, and falling off to 0.05 at +/- 25 mV. Kinetic analysis of the voltage dependence reveals that while open time constants are decreased somewhat by increases in potential, the largest effect is an increase in long closed times. Despite the channel's high conductance, it maintains a moderate selectivity for smaller anions, but will not pass larger anions such as gluconate, as determined by reversal-potential shifts. At least two substates different from the main open level are distinguishable. These properties are unlike those described for mitochondrial voltage- dependent anion channels or skeletal muscle surface membrane Cl channels and since SR Ca channels are present in equally high density in sarcoball patches, we propose these sarcoball anion channels originate from the SR. Preliminary experiments recording currents from frog SR anion channels fused into liposomes indicate that either biochemical isolation and/or alterations in lipid environment greatly decrease the channel's voltage sensitivity. These results help underline the potential significance of using sarcoballs to study SR channels. The steep voltage sensitivity of the sarcoball anion channel suggests that it could be more actively involved in the regulation of Ca2+ transport by the SR.

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Selected References

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  1. Abramcheck C. W., Best P. M. Physiological role and selectivity of the in situ potassium channel of the sarcoplasmic reticulum in skinned frog skeletal muscle fibers. J Gen Physiol. 1989 Jan;93(1):1–21. doi: 10.1085/jgp.93.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bell J. E., Miller C. Effects of phospholipid surface charge on ion conduction in the K+ channel of sarcoplasmic reticulum. Biophys J. 1984 Jan;45(1):279–287. doi: 10.1016/S0006-3495(84)84154-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Blatz A. L., Magleby K. L. Quantitative description of three modes of activity of fast chloride channels from rat skeletal muscle. J Physiol. 1986 Sep;378:141–174. doi: 10.1113/jphysiol.1986.sp016212. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Blatz A. L., Magleby K. L. Single voltage-dependent chloride-selective channels of large conductance in cultured rat muscle. Biophys J. 1983 Aug;43(2):237–241. doi: 10.1016/S0006-3495(83)84344-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bolotina V., Borecký J., Vlachová V., Baudysová M., Vyskocil F. Voltage-dependent chloride channels with several substates in excised patches from mouse neuroblastoma cells. Neurosci Lett. 1987 Jun 26;77(3):298–302. doi: 10.1016/0304-3940(87)90516-7. [DOI] [PubMed] [Google Scholar]
  6. Busath D., Szabo G. Low conductance gramicidin A channels are head-to-head dimers of beta 6.3-helices. Biophys J. 1988 May;53(5):689–695. doi: 10.1016/S0006-3495(88)83150-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. CONWAY E. J. Nature and significance of concentration relations of potassium and sodium ions in skeletal muscle. Physiol Rev. 1957 Jan;37(1):84–132. doi: 10.1152/physrev.1957.37.1.84. [DOI] [PubMed] [Google Scholar]
  8. Colombini M. Structure and mode of action of a voltage dependent anion-selective channel (VDAC) located in the outer mitochondrial membrane. Ann N Y Acad Sci. 1980;341:552–563. doi: 10.1111/j.1749-6632.1980.tb47198.x. [DOI] [PubMed] [Google Scholar]
  9. Coronado R. Planar bilayer reconstitution of calcium channels: lipid effects on single-channel kinetics. Circ Res. 1987 Oct;61(4 Pt 2):I46–I52. [PubMed] [Google Scholar]
  10. Coronado R., Rosenberg R. L., Miller C. Ionic selectivity, saturation, and block in a K+-selective channel from sarcoplasmic reticulum. J Gen Physiol. 1980 Oct;76(4):425–446. doi: 10.1085/jgp.76.4.425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Coulombe A., Duclohier H., Coraboeuf E., Touzet N. Single chloride-permeable channels of large conductance in cultured cardiac cells of new-born rats. Eur Biophys J. 1987;14(3):155–162. doi: 10.1007/BF00253840. [DOI] [PubMed] [Google Scholar]
  12. Donaldson S. K. Peeled mammalian skeletal muscle fibers. Possible stimulation of Ca2+ release via a transverse tubule-sarcoplasmic reticulum mechanism. J Gen Physiol. 1985 Oct;86(4):501–525. doi: 10.1085/jgp.86.4.501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Dulhunty A. F. Internal citrate ions reduce the membrane potential for contraction threshold in mammalian skeletal muscle fibers. Biophys J. 1988 Apr;53(4):609–616. doi: 10.1016/S0006-3495(88)83139-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Fink R. H., Stephenson D. G. Ca2+-movements in muscle modulated by the state of K+-channels in the sarcoplasmic reticulum membranes. Pflugers Arch. 1987 Aug;409(4-5):374–380. doi: 10.1007/BF00583791. [DOI] [PubMed] [Google Scholar]
  15. Franciolini F., Nonner W. Anion and cation permeability of a chloride channel in rat hippocampal neurons. J Gen Physiol. 1987 Oct;90(4):453–478. doi: 10.1085/jgp.90.4.453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Garcia A. M., Miller C. Channel-mediated monovalent cation fluxes in isolated sarcoplasmic reticulum vesicles. J Gen Physiol. 1984 Jun;83(6):819–839. doi: 10.1085/jgp.83.6.819. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Gomolla M., Gottschalk G., Lüttgau H. C. Perchlorate-induced alterations in electrical and mechanical parameters of frog skeletal muscle fibres. J Physiol. 1983 Oct;343:197–214. doi: 10.1113/jphysiol.1983.sp014888. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. HODGKIN A. L., HOROWICZ P. The effect of nitrate and other anions on the mechanical response of single muscle fibres. J Physiol. 1960 Sep;153:404–412. doi: 10.1113/jphysiol.1960.sp006542. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. HODGKIN A. L., HUXLEY A. F. A quantitative description of membrane current and its application to conduction and excitation in nerve. J Physiol. 1952 Aug;117(4):500–544. doi: 10.1113/jphysiol.1952.sp004764. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. 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]
  21. Hanrahan J. W., Alles W. P., Lewis S. A. Single anion-selective channels in basolateral membrane of a mammalian tight epithelium. Proc Natl Acad Sci U S A. 1985 Nov;82(22):7791–7795. doi: 10.1073/pnas.82.22.7791. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Herbette L., Blasie J. K., Defoor P., Fleischer S., Bick R. J., Van Winkle W. B., Tate C. A., Entman M. L. Phospholipid asymmetry in the isolated sarcoplasmic reticulum membrane. Arch Biochem Biophys. 1984 Oct;234(1):235–242. doi: 10.1016/0003-9861(84)90345-x. [DOI] [PubMed] [Google Scholar]
  23. Hymel L., Inui M., Fleischer S., Schindler H. Purified ryanodine receptor of skeletal muscle sarcoplasmic reticulum forms Ca2+-activated oligomeric Ca2+ channels in planar bilayers. Proc Natl Acad Sci U S A. 1988 Jan;85(2):441–445. doi: 10.1073/pnas.85.2.441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Irving M., Maylie J., Sizto N. L., Chandler W. K. Intrinsic optical and passive electrical properties of cut frog twitch fibers. J Gen Physiol. 1987 Jan;89(1):1–40. doi: 10.1085/jgp.89.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Kasai M., Miyamoto H. Depolarization-induced calcium release from sarcoplasmic reticulum fragments. I. Release of calcium taken up upon using ATP. J Biochem. 1976 May;79(5):1053–1066. doi: 10.1093/oxfordjournals.jbchem.a131147. [DOI] [PubMed] [Google Scholar]
  26. Khuri R. N., Bogharian K. K., Agulian S. K. Intracellular bicarbonate in single skeletal muscle fibers. Pflugers Arch. 1974;349(4):285–294. doi: 10.1007/BF00588414. [DOI] [PubMed] [Google Scholar]
  27. Kolb H. A., Brown C. D., Murer H. Identification of a voltage-dependent anion channel in the apical membrane of a Cl(-)-secretory epithelium (MDCK). Pflugers Arch. 1985 Mar;403(3):262–265. doi: 10.1007/BF00583597. [DOI] [PubMed] [Google Scholar]
  28. Kolb H. A., Ubl J. Activation of anion channels by zymosan particles in membranes of peritoneal macrophages. Biochim Biophys Acta. 1987 May 29;899(2):239–246. doi: 10.1016/0005-2736(87)90405-6. [DOI] [PubMed] [Google Scholar]
  29. Kometani T., Kasai M. Ion movement accompanied by calcium uptake of sarcoplasmic reticulum vesicles studied through the osmotic volume change by the light scattering method. J Membr Biol. 1980 Sep 30;56(2):159–168. doi: 10.1007/BF01875967. [DOI] [PubMed] [Google Scholar]
  30. Kometani T., Kasai M. Ionic permeability of sarcoplasmic reticulum vesicles measured by light scattering method. J Membr Biol. 1978 Jul 18;41(4):295–308. doi: 10.1007/BF01871994. [DOI] [PubMed] [Google Scholar]
  31. Kovács L., Ríos E., Schneider M. F. Calcium transients and intramembrane charge movement in skeletal muscle fibres. Nature. 1979 May 31;279(5712):391–396. doi: 10.1038/279391a0. [DOI] [PubMed] [Google Scholar]
  32. Krouse M. E., Schneider G. T., Gage P. W. A large anion-selective channel has seven conductance levels. Nature. 1986 Jan 2;319(6048):58–60. doi: 10.1038/319058a0. [DOI] [PubMed] [Google Scholar]
  33. Lee K. S., Tsien R. W. High selectivity of calcium channels in single dialysed heart cells of the guinea-pig. J Physiol. 1984 Sep;354:253–272. doi: 10.1113/jphysiol.1984.sp015374. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Lux H. D., Brown A. M. Patch and whole cell calcium currents recorded simultaneously in snail neurons. J Gen Physiol. 1984 May;83(5):727–750. doi: 10.1085/jgp.83.5.727. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Ma J., Coronado R. Heterogeneity of conductance states in calcium channels of skeletal muscle. Biophys J. 1988 Mar;53(3):387–395. doi: 10.1016/S0006-3495(88)83115-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Macchia D. D., Polimeni P. I., Page E. Cellular Cl content and concentration of amphibian skeletal and heart muscle. Am J Physiol. 1978 Sep;235(3):C122–C127. doi: 10.1152/ajpcell.1978.235.3.C122. [DOI] [PubMed] [Google Scholar]
  37. Mangan P. S., Colombini M. Ultrasteep voltage dependence in a membrane channel. Proc Natl Acad Sci U S A. 1987 Jul;84(14):4896–4900. doi: 10.1073/pnas.84.14.4896. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. McKinley D., Meissner G. Evidence for a K+, Na+ permeable channel in sarcoplasmic reticulum. J Membr Biol. 1978 Dec 15;44(2):159–186. doi: 10.1007/BF01976037. [DOI] [PubMed] [Google Scholar]
  39. Meissner G., McKinley D. Permeability of sarcoplasmic reticulum membrane. The effect of changed ionic environments on Ca2+ release. J Membr Biol. 1976 Dec 25;30(1):79–98. doi: 10.1007/BF01869661. [DOI] [PubMed] [Google Scholar]
  40. Meissner G. Monovalent ion and calcium ion fluxes in sarcoplasmic reticulum. Mol Cell Biochem. 1983;55(1):65–82. doi: 10.1007/BF00229243. [DOI] [PubMed] [Google Scholar]
  41. Melzer W., Rios E., Schneider M. F. Time course of calcium release and removal in skeletal muscle fibers. Biophys J. 1984 Mar;45(3):637–641. doi: 10.1016/S0006-3495(84)84203-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Miller C. Voltage-gated cation conductance channel from fragmented sarcoplasmic reticulum: steady-state electrical properties. J Membr Biol. 1978 Apr 20;40(1):1–23. doi: 10.1007/BF01909736. [DOI] [PubMed] [Google Scholar]
  43. Morimoto T., Kasai M. Reconstitution of sarcoplasmic reticulum Ca2+-ATPase vesicles lacking ion channels and demonstration of electrogenicity of Ca2+-pump. J Biochem. 1986 Apr;99(4):1071–1080. doi: 10.1093/oxfordjournals.jbchem.a135571. [DOI] [PubMed] [Google Scholar]
  44. Nakajima Y., Endo M. Release of calcium induced by 'depolarisation' of the sarcoplasmic reticulum membrane. Nat New Biol. 1973 Dec 19;246(155):216–218. doi: 10.1038/newbio246216a0. [DOI] [PubMed] [Google Scholar]
  45. Oetliker H. An appraisal of the evidence for a sarcoplasmic reticulum membrane potential and its relation to calcium release in skeletal muscle. J Muscle Res Cell Motil. 1982 Sep;3(3):247–272. doi: 10.1007/BF00713037. [DOI] [PubMed] [Google Scholar]
  46. Palade P. Drug-induced Ca2+ release from isolated sarcoplasmic reticulum. I. Use of pyrophosphate to study caffeine-induced Ca2+ release. J Biol Chem. 1987 May 5;262(13):6135–6141. [PubMed] [Google Scholar]
  47. Palade P., Vergara J. Arsenazo III and antipyrylazo III calcium transients in single skeletal muscle fibers. J Gen Physiol. 1982 Apr;79(4):679–707. doi: 10.1085/jgp.79.4.679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Peachey L. D. The sarcoplasmic reticulum and transverse tubules of the frog's sartorius. J Cell Biol. 1965 Jun;25(3 Suppl):209–231. doi: 10.1083/jcb.25.3.209. [DOI] [PubMed] [Google Scholar]
  49. Sachs F., Neil J., Barkakati N. The automated analysis of data from single ionic channels. Pflugers Arch. 1982 Dec;395(4):331–340. doi: 10.1007/BF00580798. [DOI] [PubMed] [Google Scholar]
  50. Saito A., Seiler S., Chu A., Fleischer S. Preparation and morphology of sarcoplasmic reticulum terminal cisternae from rabbit skeletal muscle. J Cell Biol. 1984 Sep;99(3):875–885. doi: 10.1083/jcb.99.3.875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Schein S. J., Colombini M., Finkelstein A. Reconstitution in planar lipid bilayers of a voltage-dependent anion-selective channel obtained from paramecium mitochondria. J Membr Biol. 1976 Dec 28;30(2):99–120. doi: 10.1007/BF01869662. [DOI] [PubMed] [Google Scholar]
  52. Schneider G. T., Cook D. I., Gage P. W., Young J. A. Voltage sensitive, high-conductance chloride channels in the luminal membrane of cultured pulmonary alveolar (type II) cells. Pflugers Arch. 1985 Aug;404(4):354–357. doi: 10.1007/BF00585348. [DOI] [PubMed] [Google Scholar]
  53. Schwarze W., Kolb H. A. Voltage-dependent kinetics of an anionic channel of large unit conductance in macrophages and myotube membranes. Pflugers Arch. 1984 Nov;402(3):281–291. doi: 10.1007/BF00585511. [DOI] [PubMed] [Google Scholar]
  54. Smith J. S., Coronado R., Meissner G. Single channel measurements of the calcium release channel from skeletal muscle sarcoplasmic reticulum. Activation by Ca2+ and ATP and modulation by Mg2+. J Gen Physiol. 1986 Nov;88(5):573–588. doi: 10.1085/jgp.88.5.573. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Smith J. S., Coronado R., Meissner G. Single-channel calcium and barium currents of large and small conductance from sarcoplasmic reticulum. Biophys J. 1986 Nov;50(5):921–928. doi: 10.1016/S0006-3495(86)83533-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Somlyo A. V., Gonzalez-Serratos H. G., Shuman H., McClellan G., Somlyo A. P. Calcium release and ionic changes in the sarcoplasmic reticulum of tetanized muscle: an electron-probe study. J Cell Biol. 1981 Sep;90(3):577–594. doi: 10.1083/jcb.90.3.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Somlyo A. V., Shuman H., Somlyo A. P. Elemental distribution in striated muscle and the effects of hypertonicity. Electron probe analysis of cryo sections. J Cell Biol. 1977 Sep;74(3):828–857. doi: 10.1083/jcb.74.3.828. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Stein P., Palade P. Sarcoballs: direct access to sarcoplasmic reticulum Ca2+-channels in skinned frog muscle fibers. Biophys J. 1988 Aug;54(2):357–363. doi: 10.1016/S0006-3495(88)82967-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Stephenson E. W. Excitation of skinned muscle fibers by imposed ion gradients. II. Influence of quercetin and ATP removal on the Ca2+-insensitive component of stimulated 45Ca efflux. J Gen Physiol. 1985 Dec;86(6):833–852. doi: 10.1085/jgp.86.6.833. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Tanifuji M., Sokabe M., Kasai M. An anion channel of sarcoplasmic reticulum incorporated into planar lipid bilayers: single-channel behavior and conductance properties. J Membr Biol. 1987;99(2):103–111. doi: 10.1007/BF01871230. [DOI] [PubMed] [Google Scholar]
  61. Thorn P., Martin R. J. A high-conductance calcium-dependent chloride channel in Ascaris suum muscle. Q J Exp Physiol. 1987 Jan;72(1):31–49. doi: 10.1113/expphysiol.1987.sp003053. [DOI] [PubMed] [Google Scholar]
  62. Tomlins B., Williams A. J. Solubilisation and reconstitution of the rabbit skeletal muscle sarcoplasmic reticulum K+ channel into liposomes suitable for patch clamp studies. Pflugers Arch. 1986 Sep;407(3):341–347. doi: 10.1007/BF00585312. [DOI] [PubMed] [Google Scholar]
  63. Vaughan-Jones R. D. Chloride activity and its control in skeletal and cardiac muscle. Philos Trans R Soc Lond B Biol Sci. 1982 Dec 1;299(1097):537–548. doi: 10.1098/rstb.1982.0150. [DOI] [PubMed] [Google Scholar]
  64. Volpe P., Bravin M., Zorzato F., Margreth A. Isolation of terminal cisternae of frog skeletal muscle. Calcium storage and release properties. J Biol Chem. 1988 Jul 15;263(20):9901–9907. [PubMed] [Google Scholar]
  65. Volpe P., Stephenson E. W. Ca2+ dependence of transverse tubule-mediated calcium release in skinned skeletal muscle fibers. J Gen Physiol. 1986 Feb;87(2):271–288. doi: 10.1085/jgp.87.2.271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Woll K. H., Leibowitz M. D., Neumcke B., Hille B. A high-conductance anion channel in adult amphibian skeletal muscle. Pflugers Arch. 1987 Dec;410(6):632–640. doi: 10.1007/BF00581324. [DOI] [PubMed] [Google Scholar]

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