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通过结构生物学研究细胞凋亡的机制。

Mechanisms of apoptosis through structural biology.

作者信息

Yan Nieng, Shi Yigong

机构信息

Department of Molecular Biology, Lewis Thomas Laboratory, Princeton University, Princeton, New Jersey 08544, USA.

出版信息

Annu Rev Cell Dev Biol. 2005;21:35-56. doi: 10.1146/annurev.cellbio.21.012704.131040.

Abstract

Apoptosis plays a central role in the development and homeostasis of metazoans. Research in the past two decades has led to the identification of hundreds of genes that govern the initiation, execution, and regulation of apoptosis. An earlier focus on the genetic and cell biological characterization has now been complemented by systematic biochemical and structural investigation, giving rise to an unprecedented level of clarity in many aspects of apoptosis. In this review, we focus on the molecular mechanisms of apoptosis by synthesizing available biochemical and structural information. We discuss the mechanisms of ligand binding to death receptors, actions of the Bcl-2 family of proteins, and caspase activation, inhibition, and removal of inhibition. Although an emphasis is given to the mammalian pathways, a comparative analysis is applied to related mechanistic information in Drosophila and Caenorhabditis elegans.

摘要

细胞凋亡在多细胞动物的发育和体内平衡中起着核心作用。过去二十年的研究已鉴定出数百个调控细胞凋亡起始、执行和调节的基因。早期对遗传和细胞生物学特征的关注,如今已通过系统的生化和结构研究得到补充,在细胞凋亡的许多方面带来了前所未有的清晰度。在本综述中,我们通过整合现有的生化和结构信息,聚焦于细胞凋亡的分子机制。我们讨论配体与死亡受体结合的机制、Bcl-2家族蛋白的作用,以及半胱天冬酶的激活、抑制和抑制解除。尽管重点是哺乳动物的信号通路,但我们也对果蝇和秀丽隐杆线虫中的相关机制信息进行了比较分析。

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