期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 284, 期 5, 页码 2967-2977出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M807269200
关键词
-
资金
- National Institutes of Health [R01-AG026660, R01-AG20670]
- Institutional Training [T32 GM073546-01A1]
- Ruth L. Kirschstein National Research Service [T32 CA062948-11A1]
- William H. and Alice Goodwin and the Commonwealth Foundation for Cancer Research
- Experimental Therapeutics Center of Memorial Sloan Kettering Cancer Center
- William Randolph Hearst Fund in Experimental Therapeutics
- American Health Assistance Foundation
gamma-Secretase is known to play a pivotal role in the pathogenesis of Alzheimer disease through production of amyloidogenic A beta 42 peptides. Early onset familial Alzheimer disease mutations in presenilin (PS), the catalytic core of gamma-secretase, invariably increase the A beta 42:A beta 40 ratio. However, the mechanism by which these mutations affect gamma-secretase complex formation and cleavage specificity is poorly understood. We show that our in vitro assay system recapitulates the effect of PS1 mutations on the A beta 42:A beta 40 ratio observed in cell and animal models. We have developed a series of small molecule affinity probes that allow us to characterize active gamma-secretase complexes. Furthermore we reveal that the equilibrium of PS1- and PS2-containing active complexes is dynamic and altered by overexpression of Pen2 or PS1 mutants and that formation of PS2 complexes is positively correlated with increased A beta 42:A beta 40 ratios. These data suggest that perturbations to gamma-secretase complex equilibrium can have a profound effect on enzyme activity and that increased PS2 complexes along with mutated PS1 complexes contribute to an increased A beta 42:A beta 40 ratio.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据