淀粉样前体蛋白
内体
化学
蛋白质前体
生物化学
淀粉样前体蛋白分泌酶
淀粉样蛋白(真菌学)
细胞生物学
生物
酶
受体
阿尔茨海默病
医学
病理
无机化学
疾病
作者
Todd E. Golde,Steven Estus,Linda H. Younkin,Dennis J. Selkoe,Steven G. Younkin
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1992-02-07
卷期号:255 (5045): 728-730
被引量:737
标识
DOI:10.1126/science.1738847
摘要
The approximately 120-kilodalton amyloid beta protein precursor (beta APP) is processed into a complex set of 8- to 12-kilodalton carboxyl-terminal derivatives that includes potentially amyloidogenic forms with the approximately 4-kilodalton amyloid beta protein (beta AP) at or near their amino terminus. In order to determine if these derivatives are processed in a secretory pathway or by the endosomal-lysosomal system, (i) deletion mutants that produce the normal set of carboxyl-terminal derivatives and shortened secreted derivatives were analyzed and (ii) the effect of inhibitors of endosomal-lysosomal processing was examined. In the secretory pathway, cleavage of the beta APP occurs at a single site within the beta AP to generate one secreted derivative and one nonamyloidogenic carboxyl-terminal fragment, whereas, in the endosomal-lysosomal system, a complex set of carboxyl-terminal derivatives is produced that includes the potentially amyloidogenic forms.
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