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阿尔茨海默病分泌酶的画像——新特征与熟悉面孔

A portrait of Alzheimer secretases--new features and familiar faces.

作者信息

Esler W P, Wolfe M S

机构信息

Center for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.

出版信息

Science. 2001 Aug 24;293(5534):1449-54. doi: 10.1126/science.1064638.

Abstract

The amyloid beta-peptide (Abeta) is a principal component of the cerebral plaques found in the brains of patients with Alzeheimer's disease (AD). This insoluble 40- to 42-amino acid peptide is formed by the cleavage of the Abeta precursor protein (APP). The three proteases that cleave APP, alpha-, beta-, and gamma-secretases, have been implicated in the etiology of AD. beta-Secretase is a membrane-anchored protein with clear homology to soluble aspartyl proteases, and alpha-secretase displays characteristics of certain membrane-tethered metalloproteases. gamma-Secretase is apparently an oligomeric complex that includes the presenilins, which may be the catalytic component of this protease. Identification of the alpha-, beta-, and gamma-secretases provides potential targets for designing new drugs to treat AD.

摘要

淀粉样β肽(Aβ)是阿尔茨海默病(AD)患者大脑中发现的脑斑的主要成分。这种不溶性的40至42个氨基酸的肽是由Aβ前体蛋白(APP)裂解形成的。裂解APP的三种蛋白酶,α-、β-和γ-分泌酶,与AD的病因有关。β-分泌酶是一种膜锚定蛋白,与可溶性天冬氨酸蛋白酶有明显的同源性,α-分泌酶具有某些膜结合金属蛋白酶的特征。γ-分泌酶显然是一种寡聚复合物,包括早老素,早老素可能是这种蛋白酶的催化成分。鉴定α-、β-和γ-分泌酶为设计治疗AD的新药提供了潜在靶点。

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