Memapsin 2, a drug target for Alzheimer's disease.

Gerald Koelsch, Robert T Turner, Lin Hong, Arun K Ghosh, Jordan Tang
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引用次数: 2

Abstract

Mempasin 2, a beta-secretase, is the membrane-anchored aspartic protease that initiates the cleavage of amyloid precursor protein leading to the production of beta-amyloid and the onset of Alzheimer's disease. Thus memapsin 2 is a major therapeutic target for the development of inhibitor drugs for the disease. Many biochemical tools, such as the specificity and crystal structure, have been established and have led to the design of potent and relatively small transition-state inhibitors. Although developing a clinically viable mempasin 2 inhibitor remains challenging, progress to date renders hope that memapsin 2 inhibitors may ultimately be useful for therapeutic reduction of beta-amyloid.

Memapsin 2,阿尔茨海默病的药物靶点。
Mempasin 2是一种β -分泌酶,是一种膜锚定的天冬氨酸蛋白酶,它启动淀粉样蛋白前体蛋白的分裂,导致β -淀粉样蛋白的产生和阿尔茨海默病的发病。因此,memapsin 2是开发该疾病抑制剂药物的主要治疗靶点。许多生化工具,如特异性和晶体结构,已经建立,并导致设计有效的和相对较小的过渡状态抑制剂。尽管开发临床可行的memapsin 2抑制剂仍然具有挑战性,但迄今为止的进展使memapsin 2抑制剂有望最终用于治疗性减少β -淀粉样蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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