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哺乳动物细胞死亡蛋白酶:一类高度保守的天冬氨酸特异性半胱氨酸蛋白酶。

Mammalian cell death proteases: a family of highly conserved aspartate specific cysteine proteases.

作者信息

Alnemri E S

机构信息

Department of Biochemistry and Molecular Pharmacology, Kimmel Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

J Cell Biochem. 1997 Jan;64(1):33-42. doi: 10.1002/(sici)1097-4644(199701)64:1<33::aid-jcb6>3.0.co;2-0.

Abstract

So far nine human aspartate-specific cysteine proteases (ASCPs) have been identified and cloned in our lab and others. Their sequence and structural homology to the nematode Ced-3 implicated them in the cell death pathway of mammalian cells. Recent evidence suggests that ASCPs initiate apoptosis by acting at or near the cell death effector level. However, it is not clear whether the activity of one or several of these enzymes is necessary for execution of apoptosis. In addition, it is not yet clear how the proenzymes of ASCPs are activated or what triggers their activation. Execution of apoptosis in higher eukaryotes is apparently more complicated than in nematodes. It is most likely that in mammalian cells this process involves the coordinated action of multiple ASCPs and multiple redundant proteolytic pathways.

摘要

到目前为止,我们实验室及其他机构已经鉴定并克隆出了九种人类天冬氨酸特异性半胱氨酸蛋白酶(ASCPs)。它们与线虫Ced-3的序列和结构同源性表明它们参与了哺乳动物细胞的细胞死亡途径。最近的证据表明,ASCPs通过在细胞死亡效应水平或其附近发挥作用来启动细胞凋亡。然而,尚不清楚这些酶中的一种或几种的活性对于细胞凋亡的执行是否必要。此外,ASCPs的酶原是如何被激活的,或者是什么触发了它们的激活,目前也尚不清楚。高等真核生物中的细胞凋亡执行过程显然比线虫中的更为复杂。在哺乳动物细胞中,这个过程很可能涉及多种ASCPs和多种冗余蛋白水解途径的协同作用。

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