首页> 美国卫生研究院文献>The Journal of Biological Chemistry >ADAM10 the Rate-limiting Protease of Regulated Intramembrane Proteolysis of Notch and Other Proteins Is Processed by ADAMS-9 ADAMS-15 and the γ-Secretase
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ADAM10 the Rate-limiting Protease of Regulated Intramembrane Proteolysis of Notch and Other Proteins Is Processed by ADAMS-9 ADAMS-15 and the γ-Secretase

机译:ADAM10调节性膜内蛋白水解的限速蛋白酶 缺口和其他蛋白质的加工由ADAMS-9ADAMS-15和 γ-分泌酶

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摘要

ADAM10 is involved in the proteolytic processing and shedding of proteins such as the amyloid precursor protein (APP), cadherins, and the Notch receptors, thereby initiating the regulated intramembrane proteolysis (RIP) of these proteins. Here, we demonstrate that the sheddase ADAM10 is also subject to RIP. We identify ADAM9 and -15 as the proteases responsible for releasing the ADAM10 ectodomain, and Presenilin/γ-Secretase as the protease responsible for the release of the ADAM10 intracellular domain (ICD). This domain then translocates to the nucleus and localizes to nuclear speckles, thought to be involved in gene regulation. Thus, ADAM10 performs a dual role in cells, as a metalloprotease when it is membrane-bound, and as a potential signaling protein once cleaved by ADAM9/15 and the γ-Secretase.
机译:ADAM10参与蛋白质的水解过程和脱落,例如淀粉样蛋白前体蛋白(APP),钙黏着蛋白和Notch受体,从而启动这些蛋白的受调节的膜内蛋白水解(RIP)。在这里,我们证明了脱脂酶ADAM10也受RIP的约束。我们确定ADAM9和-15是负责释放ADAM10胞外域的蛋白酶,而早老素/γ-分泌酶是负责释放ADAM10细胞内域(ICD)的蛋白酶。然后,该结构域易位至核并定位于核斑,据认为这与基因调控有关。因此,ADAM10在细胞中起双重作用,当被膜结合时作为金属蛋白酶,并且一旦被ADAM9 / 15和γ-分泌酶切割后作为潜在的信号蛋白。

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