Oxidative modification of creatine kinase BB in Alzheimer's disease brain

被引:224
作者
Aksenov, M
Aksenova, M
Butterfield, DA
Markesbery, WR
机构
[1] Univ Kentucky, Sanders Brown Ctr Aging, Dept Pharmacol, Lexington, KY 40536 USA
[2] Univ Kentucky, Sanders Brown Ctr Aging, Dept Chem, Lexington, KY 40536 USA
[3] Univ Kentucky, Sanders Brown Ctr Aging, Dept Pathol, Lexington, KY 40536 USA
[4] Univ Kentucky, Sanders Brown Ctr Aging, Dept Neurol, Lexington, KY 40536 USA
[5] Univ Kentucky, Ctr Membrane Sci, Lexington, KY 40536 USA
关键词
two-dimensional electrophoresis; protein carbonyls; creatine kinase; inactivation; Alzheimer's disease;
D O I
10.1046/j.1471-4159.2000.0742520.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Creatine kinase (CK) BB, a member of the CK gene family, is a predominantly cytosolic CK isoform in the brain and plays a key role in regulation of the ATP level in neural cells. CK BB levels are reduced in brain regions affected by neurodegeneration in Alzheimer's disease (AD), Pick's disease, and Lewy body dementia, and this reduction is not a result of decreased mRNA levels. This study demonstrates that posttranslational modification of CK BB plays a role in the decrease of CK activity in AD brain. The specific CK BB activity and protein carbonyl content were determined in brain extracts of six AD and six age-matched control subjects. CK BB activity per microgram of immunoreactive CK BB protein was lower in AD than in control brain extracts, indicating the presence of inactive CK BB molecules. The analysis of specific protein carbonyl levels in CK BB, performed by two-dimensional fingerprinting of oxidatively modified proteins, identified CK BB as one of the targets of protein oxidation in the AD brain. The increase of protein carbonyl content in CK BB provides evidence that oxidative posttranslational modification of CK BB plays a role in the loss of CK BB activity in AD.
引用
收藏
页码:2520 / 2527
页数:8
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