Wolfe Michael S
Center for Neurologic Diseases at Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Sci Aging Knowledge Environ. 2003 Mar 19;2003(11):PE7. doi: 10.1126/sageke.2003.11.pe7.
Gamma-secretase catalyzes intramembrane proteolysis of the amyloid beta protein precursor, a process closely linked to the development of Alzheimer's disease. This protease also cleaves the transmembrane domain of the Notch receptor as part of a signaling pathway that is essential for proper embryonic development. Recent findings suggest that gamma-secretase is a complex of at least four integral membrane proteins: presenilin, nicastrin, Aph-1, and Pen-2. Assembly of these four components apparently leads to autocleavage of presenilin into two subunits that together compose the intramembranous active site of gamma-secretase. Understanding the mechanism of this unusual enzyme is important, as it is both a key therapeutic target and a founding member of a newly discovered class of intramembrane-cleaving proteases.
γ-分泌酶催化淀粉样β蛋白前体的膜内蛋白水解,这一过程与阿尔茨海默病的发展密切相关。作为正常胚胎发育所必需的信号通路的一部分,这种蛋白酶还切割Notch受体的跨膜结构域。最近的研究结果表明,γ-分泌酶是一种至少由四种整合膜蛋白组成的复合物:早老素、尼卡斯特林、Aph-1和Pen-2。这四种成分的组装显然导致早老素自动切割成两个亚基,这两个亚基共同构成γ-分泌酶的膜内活性位点。了解这种特殊酶的作用机制很重要,因为它既是一个关键的治疗靶点,也是新发现的一类膜内切割蛋白酶的首个成员。