SINGLE ANION CHANNELS RECONSTITUTED FROM CARDIAC MITOPLASTS

被引:37
作者
HAYMAN, KA [1 ]
SPURWAY, TD [1 ]
ASHLEY, RH [1 ]
机构
[1] UNIV EDINBURGH, DEPT BIOCHEM, GEORGE SQ, EDINBURGH EH8 9XD, SCOTLAND
关键词
ANION CHANNEL; MITOCHONDRION; PLANAR BILAYER; SUBSTATE;
D O I
10.1007/BF02505762
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ion channels from sheep cardiac mitoplast (inverted inner mitochondrial membrane vesicle) preparations were incorporated into voltage-clamped planar lipid bilayers. The appearance of anion rather than cation channels could be promoted by exposing the bilayers to osmotic gradients formed by Cl- salts of large, relatively impermeant, cations at a pH of 8.8. Two distinct activities were identified. These comprised a multi-substate anion channel of intermediate conductance (approximately 60 pS in 300 vs. 50 mm choline Cl, approximately 100 pS in symmetric 150 mm KCl), and a lower-conductance anion channel (approximately 25 or approximately 50 pS in similar conditions), which only displayed two well-defined substates, at approximately 25 and approximately 50% of the fully open state. The larger channels were not simple multiples of the lower-conductance channels, but both discriminated poorly, and to a similar extent, between anions and cations (P(Cl-)/P(choline+) approximately 12, P(Cl-)/PK+ approximately 8). The lower-conductance channel was only minimally selective between different anions (P(NO3-)(1.0) = P(CI)>P(Br-)>P(I-)>P(SCN-)(0.8)), and its conductance failed to saturate even in high (>1.0 M) activities of KCl. The channels were not obviously voltage dependent, and they were unaffected by 0.5 mM SITS, H2O2, propranolol, quinine or amitriptyline, or by 2 mM ATP, or by variations in pH (5.5-8.8). Ca2+ and Mg2+ did not alter single channel activity, but did modify single current amplitudes in the lower-conductance channel. This effect, together with voltage-dependent substate behavior, is described in the following paper.
引用
收藏
页码:181 / 190
页数:10
相关论文
共 39 条
[1]   SELECTIVE EFFECT OF INHIBITORS ON INNER MITOCHONDRIAL-MEMBRANE CHANNELS [J].
ANTONENKO, YN ;
KINNALLY, KW ;
PERINI, S ;
TEDESCHI, H .
FEBS LETTERS, 1991, 285 (01) :89-93
[2]   IDENTIFICATION OF ANION AND CATION PATHWAYS IN THE INNER MITOCHONDRIAL-MEMBRANE BY PATCH CLAMPING OF MOUSE-LIVER MITOPLASTS [J].
ANTONENKO, YN ;
KINNALLY, KW ;
TEDESCHI, H .
JOURNAL OF MEMBRANE BIOLOGY, 1991, 124 (02) :151-158
[3]   ACTIVATION AND CONDUCTANCE PROPERTIES OF RYANODINE-SENSITIVE CALCIUM CHANNELS FROM BRAIN MICROSOMAL-MEMBRANES INCORPORATED INTO PLANAR LIPID BILAYERS [J].
ASHLEY, RH .
JOURNAL OF MEMBRANE BIOLOGY, 1989, 111 (02) :179-189
[4]   BIOCHEMICAL AND ULTRASTRUCTURAL PROPERTIES OF A MITOCHONDRIAL INNER MEMBRANE FRACTION DEFICIENT IN OUTER MEMBRANE AND MATRIX ACTIVITIES [J].
CHAN, TL ;
GREENAWALT, JW ;
PEDERSEN, PL .
JOURNAL OF CELL BIOLOGY, 1970, 45 (02) :291-+
[5]  
COLOMBINI M, 1986, ION CHANNEL RECONSTI, pCH22
[6]   EVIDENCE FOR THE PRESENCE OF A REVERSIBLE CA-2+-DEPENDENT PORE ACTIVATED BY OXIDATIVE STRESS IN HEART-MITOCHONDRIA [J].
CROMPTON, M ;
COSTI, A ;
HAYAT, L .
BIOCHEMICAL JOURNAL, 1987, 245 (03) :915-918
[8]   FUNCTIONAL EVIDENCE OF A TRANSMEMBRANE CHANNEL WITHIN THE CA2+ TRANSPORT ATPASE OF SARCOPLASMIC-RETICULUM [J].
DEMEIS, L ;
INESI, G .
FEBS LETTERS, 1992, 299 (01) :33-35
[9]   ACTION OF CYCLOSPORINE ON MITOCHONDRIAL CALCIUM FLUXES [J].
FOURNIER, N ;
DUCET, G ;
CREVAT, A .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1987, 19 (03) :297-303
[10]   CHLORIDE CHANNELS OF BIOLOGICAL-MEMBRANES [J].
FRANCIOLINI, F ;
PETRIS, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1031 (02) :247-259