A simplified and reliable assay for complex I in human blood lymphocytes

被引:9
作者
de Wit, L. E. A.
Spruijt, L.
Schoonderwoerd, G. C.
de Coo, I. F. M.
Smeets, H. J. M.
Scholte, H. R.
Sluiter, W. [1 ]
机构
[1] Erasmus MC, Mitochondria Res Unit, Dept Biochem, Rotterdam, Netherlands
[2] Erasmus MC, Dept Clin Genet, NL-3000 CA Rotterdam, Netherlands
[3] Erasmus MC, Dept Neurol, NL-3000 CA Rotterdam, Netherlands
[4] Univ Maastricht, Dept Genet & Cell Biol, Maastricht, Netherlands
关键词
mitochondria; oxidative phosphorylation (OXPHOS); respiratory chain; rotenone-sensitive NADH : coenzyme Q oxidoreductase; (complex 1); rotenone-insensitive NADH : coenzyme Q oxidoreductase (RINQ);
D O I
10.1016/j.jim.2007.07.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Complex I activity of the mitochondrial respiratory chain is difficult to measure in blood lymphocytes because of the limited access of substrates to the enzyme complex in these cells. The results of the present study show that permeabilization of human blood lymphocytes in the presence of protease inhibitors by three cycles of freeze-thawing enables reproducible detection of the rotenone-sensitive complex I activity. To that end, the water-soluble coenzyme Q(10) analogue CoQ(1) and a relatively high concentration of blood lymphocytes were combined in small quartz cuvettes so that the amount of blood needed for this assay remained low. The relationship between the initial rate of NADH oxidation by complex I and the protein concentration was quasi-linear. The fractional inhibition of the total NADH:CoQ(1) oxidoreductase by a saturating concentration of rotenone decreased sharply at CoQ(1) concentrations higher than 20 mu M, which is indicative, but does not prove the involvement of a second CoQ(1) binding site at complex I. Since the present complex I assay requires only a small amount of blood, the functionality of this important respiratory chain complex can be assessed in an easy and reliable manner not only in adult patients but also in children suspected to have a mitochondrial disease. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:76 / 82
页数:7
相关论文
共 23 条
[1]   Assaying mitochondrial respiratory complex activity in mitochondria isolated from human cells and tissues [J].
Birch-Machin, MA ;
Turnbull, DM .
METHODS IN CELL BIOLOGY, VOL 65: MITOCHONDRIA, 2001, 65 :97-117
[2]   Respiratory chain analysis of skin fibroblasts in mitochondrial disease [J].
Cameron, JM ;
Levandovskiy, V ;
MacKay, N ;
Robinson, BH .
MITOCHONDRION, 2004, 4 (5-6) :387-394
[3]   REFERENCE CHARTS FOR RESPIRATORY-CHAIN ACTIVITIES IN HUMAN TISSUES [J].
CHRETIEN, D ;
RUSTIN, P ;
BOURGERON, T ;
ROTIG, A ;
SAUDUBRAY, JM ;
MUNNICH, A .
CLINICA CHIMICA ACTA, 1994, 228 (01) :53-70
[4]   Assay of mitochondrial respiratory chain complex I in human lymphocytes and cultured skin fibroblasts [J].
Chretien, D ;
Bénit, P ;
Chol, M ;
Lebon, S ;
Rötig, A ;
Munnich, A ;
Rustin, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 301 (01) :222-224
[5]   Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy [J].
Cock, HR ;
Cooper, JM ;
Schapira, AHV .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 165 (01) :10-17
[6]  
DeVries DD, 1996, AM J HUM GENET, V58, P703
[7]  
FLEISCHER S, 1967, J LIPID RES, V8, P170
[8]   Functional characterization of mitochondria in neutrophils: a role restricted to apoptosis [J].
Maianski, NA ;
Geissler, J ;
Srinivasula, SM ;
Alnemri, ES ;
Roos, D ;
Kuijpers, TW .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (02) :143-153
[9]   Catalytic activity of Complex I in cell lines that possess replacement mutations in the ND genes in Leber's hereditary optic neuropathy [J].
Majander, A ;
Finel, M ;
Savontaus, ML ;
Nikoskelainen, E ;
Wikstrom, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 239 (01) :201-207
[10]   ELECTRON-TRANSFER PROPERTIES OF NADH - UBIQUINONE REDUCTASE IN THE ND1/3460 AND THE ND4/11778 MUTATIONS OF THE LEBER HEREDITARY OPTIC NEURORETINOPATHY (LHON) [J].
MAJANDER, A ;
HUOPONEN, K ;
SAVONTAUS, ML ;
NIKOSKELAINEN, E ;
WIKSTROM, M .
FEBS LETTERS, 1991, 292 (1-2) :289-292