Measuring the quantity and activity of mitochondrial electron transport chain complexes in tissues of central nervous system using blue native polyacrylamide gel electrophoresis

被引:78
作者
Jung, C
Higgins, CMJ
Xu, ZS
机构
[1] Univ Massachusetts, Sch Med, Dept Mol Pharmacol & Biochem, Worcester, MA 01655 USA
[2] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
[3] Univ Massachusetts, Sch Med, Program Neurosci, Worcester, MA 01655 USA
关键词
respiratory enzyme; neurodegenerative disease; energy; ATP; neuronal degeneration; ALS;
D O I
10.1006/abio.2000.4813
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial dysfunction and degeneration are associated with many neurodegenerative disorders. A dysfunctional mitochondrial electron transport chain (ETC) impairs ATP production and accelerates the generation of free radicals. To evaluate mitochondrial function, reliable methods are needed. Conventional spectrophotometric assays may not eliminate interference from nonspecific enzyme activities and do not measure quantities of specific ETC complexes. Blue native polyacrylamide gel electrophoresis (BN-PAGE) has been used to resolve mitochondrial ETC complexes. Combined with histochemical staining, it has also been applied to measure ETC enzyme activities in muscles. The current study is to determine (1) whether BN-PAGE can be used to detect ETC complexes from different regions of the central nervous system (CNS) and (2) the quantitative range of BN-PAGE in measuring the amounts and activities of different ETC complexes. By systematically varying the protein amount and the time of histochemical reactions, we have found linear ranges comparable to spectrophotometric assays for measuring enzyme activities of several ETC complexes. In addition, we found linear ranges for measuring protein quantities in several ETC complexes. These results demonstrate that BN-PAGE can be used to measure the amount and activity of the ETC enzymes from the nerve tissues and, thus, can be applied to evaluate the functional changes of mitochondria in neurodegenerative disorders. (C) 2000 Academic Press.
引用
收藏
页码:214 / 223
页数:10
相关论文
共 24 条
[1]   Mitochondria, free radicals, and neurodegeneration [J].
Beal, MF .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (05) :661-666
[2]  
Browne SE, 1998, J NEUROCHEM, V71, P281
[3]   An evaluation of the role of mitochondria in neurodegenerative diseases: mitochondrial mutations and oxidative pathology, protective nuclear responses, and cell death in neurodegeneration [J].
Cassarino, DS ;
Bennett, JP .
BRAIN RESEARCH REVIEWS, 1999, 29 (01) :1-25
[4]  
Darley-Usmar V. M., 1987, MITOCHONDRIA PRACTIC
[5]  
Dubowitz V., 1985, MUSCLE BIOPSY PRACTI
[6]   ASSAY CONDITIONS FOR THE MITOCHONDRIAL NADH - COENZYME-Q OXIDOREDUCTASE [J].
ESTORNELL, E ;
FATO, R ;
PALLOTTI, F ;
LENAZ, G .
FEBS LETTERS, 1993, 332 (1-2) :127-131
[7]   Separation by blue native and colorless native polyacrylamide gel electrophoresis of the oxidative phosphorylation complexes of yeast mitochondria solubilized by different detergents: Specific staining of the different complexes [J].
GrandierVazeille, X ;
Guerin, M .
ANALYTICAL BIOCHEMISTRY, 1996, 242 (02) :248-254
[8]  
Hatefi Y, 1979, Methods Enzymol, V56, P577
[9]   ANALYSIS OF OXIDATIVE-PHOSPHORYLATION COMPLEXES IN CULTURED HUMAN FIBROBLASTS AND AMNIOCYTES BY BLUE-NATIVE-ELECTROPHORESIS USING MITOPLASTS ISOLATED WITH THE HELP OF DIGITONIN [J].
KLEMENT, P ;
NIJTMANS, LGJ ;
VANDENBOGERT, C ;
HOUSTEK, J .
ANALYTICAL BIOCHEMISTRY, 1995, 231 (01) :218-224
[10]  
Kong JM, 1998, J NEUROSCI, V18, P3241