ALZHEIMERS-DISEASE AMYLOID BETA-CLIPPING ENZYME (APP SECRETASE) - IDENTIFICATION, PURIFICATION, AND CHARACTERIZATION OF THE ENZYME

被引:67
作者
TAGAWA, K
KUNISHITA, T
MARUYAMA, K
YOSHIKAWA, K
KOMINAMI, E
TSUCHIYA, T
SUZUKI, K
TABIRA, T
SUGITA, H
ISHIURA, S
机构
[1] NATL INST NEUROSCI,TOKYO,JAPAN
[2] PSYCHIAT RES INST TOKYO,DEPT MOLEC BIOL,TOKYO 156,JAPAN
[3] JUNTENDO UNIV,SCH MED,DEPT BIOCHEM,TOKYO 113,JAPAN
[4] SOPHIA UNIV,FAC SCI & TECHNOL,DEPT CHEM,TOKYO 102,JAPAN
[5] TOKYO METROPOLITAN INST MED SCI,DEPT MOLEC BIOL,TOKYO 113,JAPAN
关键词
D O I
10.1016/0006-291X(91)91994-N
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
Alzheimer's disease (AD) is the most frequent cause of dementia, although no genetic abnormality has been identified. Recent studies have elucidated the molecular defect in AD, including the abnormal deposition of amyloid β peptide ( β A4) in senile plaques of affected individuals. Normal brain contains the enzyme, APP secretase, which cleaves inside the β A4 portion of the precursor protein (APP); abnormal processing of APP occurs in AD brain. Until now, no evidence has been provided that APP secretase is an intracellular proteinase. We have now prepared two synthetic substrates of APP secretase, both of which contain the cleavage point and are much more sensitive than substrates previously available to identify APP secretase. Using these substrates, we found an intracellular proteinase that has APP secretase activity. This proteinase has been identified as cathepsin B. © 1991.
引用
收藏
页码:377 / 387
页数:11
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