AHA- HETERODIMER OF A CLASS-2 UNCOUPLER - PENTACHLOROPHENOL

被引:14
作者
BARSTAD, AW
PEYTON, DH
SMEJTEK, P
机构
[1] PORTLAND STATE UNIV,DEPT PHYS,PORTLAND,OR 97207
[2] PORTLAND STATE UNIV,DEPT CHEM,PORTLAND,OR 97207
[3] PORTLAND STATE UNIV,ENVIRONM SCI & RESOURCES PROGRAM,PORTLAND,OR 97207
关键词
PENTACHLOROPHENOL; UNCOUPLER; LIPID MEMBRANE; PROTON TRANSPORT;
D O I
10.1016/0005-2728(93)90065-N
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
AHA- heterodimers formed by association of neutral molecules of weak acid (HA) with its conjugate anion (A-) have been proposed to be the charged membrane-permeable species of class-2 uncouplers. Past attempts to extract and identify AHA-heterodimers failed. We have measured optical spectra of HA + A- (1:1) solutions of pentachlorophenol (PCP) in various solvents and in the presence of PC liposomes. Optical studies were supplemented by nuclear magnetic resonance measurements of HA + A- (1: 1) solutions of PCP in dichloroethane to gain insight into the formation of AHA- species in lipid membranes. From these experiments, we found evidence for AHA- formation in non-hydrogen-bonding solvents, then reported the AHA-formation constant K(f) and the molar absorptivity epsilon(AHA-)(lambda). K(f) decreases with increasing dielectric constant, kappa, from 1210 +/- 130 M-1 for dichloroethane (kappa 10.7), to 340 +/- 34 M-1 for acetonitrile (kappa 37.5); K(f) also decreases with increasing concentration of water. In hydrogen-bonding solvents, octanol (kappa 10.3) and methanol (kappa 33.5) and in liposomes, AHA- heterodimers are not observed optically. We estimate K(f) for PCP in lipid bilayers from a combination of data on membrane electrical conductivity and surface density of adsorbed PCP. Our estimate for lipid bilayer, 0.005 < K(f) < 0.5 M-1, is consistent with our inability to detect the AHA- species optically in liposome suspensions. We propose that penetration of water into the membrane inhibits formation of AHA- in lipid bilayers.
引用
收藏
页码:262 / 270
页数:9
相关论文
共 51 条
[21]  
LEBEDEV AV, 1973, MEMBRANE BIOPHYSICS, P406
[22]  
LINDANE P, 1970, INORG CHEM, V9, P757
[23]   H-1-NMR AND IR STUDIES OF HYDROGEN-BONDED COMPLEXES .3. PROTON-TRANSFER IN 4-NITROBENZOIC ACID - PHENOLATE SYSTEMS IN ACETONITRILE [J].
MAGONSKI, J ;
PAWLAK, Z .
JOURNAL OF MOLECULAR STRUCTURE, 1982, 80 (1-4) :243-250
[24]  
MAIER T, 1972, INORG CHEM, V8, P1861
[25]   MECHANISM OF ACTION OF DNP ON PHOSPHOLIPID BILAYER MEMBRANES [J].
MCLAUGHLIN, S .
JOURNAL OF MEMBRANE BIOLOGY, 1972, 9 (04) :361-+
[26]   TRANSPORT OF PROTONS ACROSS MEMBRANES BY WEAK ACIDS [J].
MCLAUGHLIN, SGA ;
DILGER, JP .
PHYSIOLOGICAL REVIEWS, 1980, 60 (03) :825-863
[27]   QUANTITATIVE RELATIONSHIP BETWEEN PROTONOPHORIC AND UNCOUPLING ACTIVITIES OF ANALOGS OF SF6847 (2,6-DI-TERT-BUTYL-4-(2',2'-DICYANOVINYL)PHENOL) [J].
MIYOSHI, H ;
NISHIOKA, T ;
FUJITA, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 891 (03) :293-299
[28]   QUANTITATIVE-ANALYSIS OF UNCOUPLING ACTIVITY OF SUBSTITUTED PHENOLS WITH A PHYSICOCHEMICAL SUBSTITUENT AND MOLECULAR-PARAMETERS [J].
MIYOSHI, H ;
TSUJISHITA, H ;
TOKUTAKE, N ;
FUJITA, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1016 (01) :99-106
[29]   QUANTITATIVE RELATIONSHIP BETWEEN PROTONOPHORIC AND UNCOUPLING ACTIVITIES OF SUBSTITUTED PHENOLS [J].
MIYOSHI, H ;
NISHIOKA, T ;
FUJITA, T .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 891 (02) :194-204
[30]  
NAGLE JF, 1987, J BIOENERG BIOMEMBR, V19, P413