Capillary electrophoresis of cardiolipin with on-line dye interaction and spectrophotometric detection

被引:30
作者
Qi, LN
Danielson, ND [1 ]
Dai, Q
Lee, RM
机构
[1] Miami Univ, Dept Chem & Biochem, Oxford, OH 45056 USA
[2] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
关键词
apoptosis; capillary electrophoresis; cardiolipin; mitochondria; 10-N-nonylacridine orange; spectrophotometric detection;
D O I
10.1002/elps.200305448
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cardiolipin is an important phospholipid present in the mitochondrial inner membrane. It plays a key function in mitochondrial respiration by interacting with many enzymes or cofactors related to oxidative phosphorylation complexes. We have determined the concentration of cardiolipin using on-line 10-N-nonyl acridine orange (NAO) dye interaction capillary electrophoresis (CE) and spectrophotometric detection with a sample throughput of 3 min. In addition to the presence of 0.1 mm NAO, the background electrolyte (BGE) composition has been set at 80% methanol-10% acetonitrile-10% H2O (all v/v) to provide both good solubility and the maximum absorbance enhancement at 497 nm for the NAO-cardiolipin complex as compared to NAO alone. Sample consumption for each injection is about 57 nL. A calibration curve is established from 0.5 muM to 0.1 mM with R-2 = 0.9912 with a detection limit of 0.05 muM for cardiolipin. In a blind study, actual mitochondrial cell membrane samples in the muL range before or after UV light exposure were analyzed using the CE method. Cardiolipin concentration decreased in the different parts of the membrane sample upon UV photolysis of the cells. Support for the theory that UV light can induce cardiolipin translocation from the inner membrane (IM) to the outer membrane (OM) was indicated by a significant percentage increase of cardiolipin (as measured by the cardiolipin in the OM as compared to the sum total in the OM and IM) from 30.7 +/- 2.4% before UV light photolysis to 38.3 +/- 2.2% after UV irradiation.
引用
收藏
页码:1680 / 1686
页数:7
相关论文
共 47 条
[31]   Cardiolipin binds nonyl acridine orange by aggregating the dye at exposed hydrophobic domains on bilayer surfaces [J].
Mileykovskaya, E ;
Dowhan, W ;
Birke, RL ;
Zheng, DH ;
Lutterodt, L ;
Haines, TH .
FEBS LETTERS, 2001, 507 (02) :187-190
[32]  
MOWER DA, 1994, J IMMUNOL, V152, P4832
[33]   HIGHLY SENSITIVE DETERMINATION AND CHARACTERIZATION OF INTACT CELLULAR ESTER-LINKED PHOSPHOLIPIDS USING LIQUID-CHROMATOGRAPHY PLASMA SPRAY MASS-SPECTROMETRY [J].
ODHAM, G ;
VALEUR, A ;
MICHELSEN, P ;
ARONSSON, E ;
MCDOWALL, M .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1988, 434 (01) :31-41
[34]  
Pangborn MC, 1941, P SOC EXP BIOL MED, V48, P484, DOI 10.3181/00379727-48-13365P
[35]   CHOLESTEROL CONTENT OF OUTER AND INNER MEMBRANES OF GUINEA-PIG LIVER MITOCHONDRIA [J].
PARSONS, DF ;
YANO, Y .
BIOCHIMICA ET BIOPHYSICA ACTA, 1967, 135 (02) :362-&
[36]   N-10-NONYL ACRIDINE-ORANGE INTERACTS WITH CARDIOLIPIN AND ALLOWS THE QUANTIFICATION OF THIS PHOSPHOLIPID IN ISOLATED-MITOCHONDRIA [J].
PETIT, JM ;
MAFTAH, A ;
RATINAUD, MH ;
JULIEN, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1992, 209 (01) :267-273
[37]  
RAGAN CIW, 1995, MITOCHONDRIA PRACTIC
[38]   Separation of phospholipids by nonaqueous capillary electrophoresis with electrospray ionisation mass spectrometry [J].
Raith, K ;
Wolf, R ;
Wagner, J ;
Neubert, RHH .
JOURNAL OF CHROMATOGRAPHY A, 1998, 802 (01) :185-188
[39]  
Rütters H, 2000, RAPID COMMUN MASS SP, V14, P122, DOI 10.1002/(SICI)1097-0231(20000130)14:2<122::AID-RCM844>3.0.CO
[40]  
2-R