Suppr超能文献

X11α蛋白会损害淀粉样前体蛋白的γ-切割,但不会损害其β-切割。

X11alpha impairs gamma- but not beta-cleavage of amyloid precursor protein.

作者信息

King Gwendalyn D, Cherian Kay, Turner R Scott

机构信息

Neuroscience Program, University of Michigan, Ann Arbor, Michigan 48105, USA.

出版信息

J Neurochem. 2004 Feb;88(4):971-82. doi: 10.1046/j.1471-4159.2003.02234.x.

Abstract

The phosphotyrosine binding domain of the neuronal protein X11alpha/mint-1 binds to the C-terminus of amyloid precursor protein (APP) and inhibits catabolism to beta-amyloid (Abeta), but the mechanism of this effect is unclear. Coexpression of X11alpha or its PTB domain with APPswe inhibited secretion of Abeta40 but not APPsbetaswe, suggesting inhibition of gamma- but not beta-secretase. To further probe cleavage(s) inhibited by X11alpha, we coexpressed beta-secretase (BACE-1) or a component of the gamma-secretase complex (PS-1Delta9) with APP, APPswe, or C99, with and without X11alpha, in HEK293 cells. X11alpha suppressed the PS-1Delta9-induced increase in Abeta42 secretion generated from APPswe or C99. However, X11alpha did not impair BACE-1-mediated proteolysis of APP or APPswe to C99. In contrast to impaired gamma-cleavage of APPswe, X11alpha or its PTB domain did not inhibit gamma-cleavage of NotchDeltaE to NICD (the Notch intracellular domain). The X11alpha PDZ-PS.1Delta9 interaction did not affect gamma-cleavage activity. In a cell-free system, X11alpha did not inhibit the catabolism of APP C-terminal fragments. These data suggest that X11alpha may inhibit Abeta secretion from APP by impairing its trafficking to sites of active gamma-secretase complexes. By specifically targeting substrate instead of enzyme X11alpha may function as a relatively specific gamma-secretase inhibitor.

摘要

神经元蛋白X11α/mint-1的磷酸酪氨酸结合结构域与淀粉样前体蛋白(APP)的C末端结合,并抑制其向β-淀粉样蛋白(Aβ)的分解代谢,但其作用机制尚不清楚。X11α或其PTB结构域与APPswe共表达可抑制Aβ40的分泌,但不影响APPsbetaswe的分泌,提示其抑制的是γ-分泌酶而非β-分泌酶。为进一步探究X11α抑制的切割过程,我们在HEK293细胞中,将β-分泌酶(BACE-1)或γ-分泌酶复合物的一个组分(PS-1Delta9)与APP、APPswe或C99共表达,同时有或没有X11α。X11α抑制了PS-1Delta9诱导的由APPswe或C99产生的Aβ42分泌增加。然而,X11α并不损害BACE-1介导的APP或APPswe向C99的蛋白水解。与APPswe的γ-切割受损相反,X11α或其PTB结构域并不抑制NotchDeltaE向NICD(Notch细胞内结构域)的γ-切割。X11α与PS.1Delta9的PDZ相互作用并不影响γ-切割活性。在无细胞体系中,X11α并不抑制APP C末端片段的分解代谢。这些数据提示,X11α可能通过损害APP向活性γ-分泌酶复合物位点的转运来抑制Aβ从APP的分泌。通过特异性靶向底物而非酶,X11α可能作为一种相对特异的γ-分泌酶抑制剂发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验