Cardiolipin binds nonyl acridine orange by aggregating the dye at exposed hydrophobic domains on bilayer surfaces

被引:109
作者
Mileykovskaya, E
Dowhan, W
Birke, RL
Zheng, DH
Lutterodt, L
Haines, TH
机构
[1] CUNY City Coll, Dept Chem, New York, NY 10031 USA
[2] Univ Texas, Sch Med, Houston, TX USA
关键词
10-N-nonyl acridine orange; cardiolipin; fluorescence emission; cardiolipin pK; lipid phase separation; Escherichia coli;
D O I
10.1016/S0014-5793(01)02948-9
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
10-N-Nonyl acridine orange (NAO) has been used at low concentrations as a fluorescent indicator for cardiolipin (CL) in membranes and bilayers. The mechanism of its selective fluorescence in the presence of CL, and not any other phospholipids, is not understood. The dye might recognize CL by its high pK (pK(2) > 8.5). To investigate that, we established that NAO does not exhibit a pK in a pH range between 2.3 and 10.0. A second explanation is that the dye aggregates at hydrophobic domains on bilayers exposed by the CL. We found that a similar spectral shift occurs in the absence of CL in a concentrated solution of the dye in methanol and in the solid state. A model is proposed in which the nonyl group inserts in the bilayer at the hydrophobic surface generated by the presence of four chains on the phospholipid. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:187 / 190
页数:4
相关论文
共 22 条
[1]   Isolation and characterization of the gene (CLS1) encoding cardiolipin synthase in Saccharomyces cerevisiae [J].
Chang, SC ;
Heacock, PN ;
Mileykovskaya, E ;
Voelker, DR ;
Dowhan, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (24) :14933-14941
[2]  
CHENEVAL D, 1985, J BIOL CHEM, V260, P3003
[3]   HYDROPHOBIC ACRIDINE-DYES FOR FLUORESCENCE STAINING OF MITOCHONDRIA IN LIVING CELLS .2. COMPARISON OF STAINING OF LIVING AND FIXED HELA-CELLS WITH NAO AND DPPAO [J].
ERBRICH, U ;
SEPTINUS, M ;
NAUJOK, A ;
ZIMMERMANN, HW .
HISTOCHEMISTRY, 1984, 80 (04) :385-388
[4]  
GALLET PF, 1995, EUR J BIOCHEM, V228, P113, DOI 10.1111/j.1432-1033.1995.0113o.x
[5]  
GARCIA FM, 2000, FEBS LETT, V478, P290
[6]   INTERACTIONS OF ACRIDINE-ORANGE WITH DOUBLE-STRANDED NUCLEIC-ACIDS - SPECTRAL AND AFFINITY STUDIES [J].
KAPUSCINSKI, J ;
DARZYNKIEWICZ, Z .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 1987, 5 (01) :127-143
[7]   PH-DISSOCIATION CHARACTERISTICS OF CARDIOLIPIN AND ITS 2'-DEOXY ANALOG [J].
KATES, M ;
SYZ, JY ;
GOSSER, D ;
HAINES, TH .
LIPIDS, 1993, 28 (10) :877-882
[8]   USE OF NONYL ACRIDINE-ORANGE AND RHODAMINE-123 TO FOLLOW BIOSYNTHESIS AND FUNCTIONAL ASSEMBLY OF MITOCHONDRIAL-MEMBRANE DURING L1210 CELL-CYCLE [J].
LEPRAT, P ;
RATINAUD, MH ;
MAFTAH, A ;
PETIT, JM ;
JULIEN, R .
EXPERIMENTAL CELL RESEARCH, 1990, 186 (01) :130-137
[9]   A NEW METHOD FOR TESTING CELL AGING USING 2 MITOCHONDRIA SPECIFIC FLUORESCENT-PROBES [J].
LEPRAT, P ;
RATINAUD, MH ;
JULIEN, R .
MECHANISMS OF AGEING AND DEVELOPMENT, 1990, 52 (2-3) :149-167
[10]   SPECIFIC INTERACTION OF THE NEW FLUORESCENT DYE 10-N-NONYL ACRIDINE-ORANGE WITH INNER MITOCHONDRIAL-MEMBRANE - A LIPID-MEDIATED INHIBITION OF OXIDATIVE-PHOSPHORYLATION [J].
MAFTAH, A ;
PETIT, JM ;
JULIEN, R .
FEBS LETTERS, 1990, 260 (02) :236-240