The catalytic core of γ-secretase:: Presenilin revisited

被引:33
作者
Steiner, Harald [1 ]
机构
[1] Univ Munich, Lab Neurodegenerat Dis Res, Dept Biochem, Adolf Butenandt Inst, D-80336 Munich, Germany
关键词
Alzheimer's disease; Amyloid beta-peptide; presenilin; gamma-secretase;
D O I
10.2174/156720508783954677
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Mutations in the presenilin 1 (PS1) gene are the major cause of familial Alzheimer's disease (AD). They effect an increased production of the highly neurotoxic 42 amino acid variant of the amyloid-beta peptide (A beta) which is believed to initiate the disease. A beta is the product of two consecutive cleavages of the beta-amyloid precursor protein (APP) by two proteases, beta-secretase and gamma-secretase. The latter enzyme has been identified as an intramembrane-cleaving multiprotein complex that apart from APP cleaves a large number of other type I transmembrane proteins. PS1 and its homologue PS2 are essential for gamma-secretase cleavage and more than a decade after their discovery it is now firmly established that they function as catalytic subunits of gamma-secretase. This review recapitulates the findings that led to this conclusion as well as the further progress made on the function of PS as gamma-secretase since then.
引用
收藏
页码:147 / 157
页数:11
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