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细胞凋亡的调控:揭示结合决定因素。

Regulation of apoptosis: uncovering the binding determinants.

作者信息

Hinds Mark G, Day Catherine L

机构信息

The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville 3050, Australia.

出版信息

Curr Opin Struct Biol. 2005 Dec;15(6):690-9. doi: 10.1016/j.sbi.2005.10.003. Epub 2005 Nov 2.

Abstract

Eukaryotic cells use complex networks of signal transduction proteins to make decisions about whether to differentiate, grow or die. In the case of apoptosis, which is responsible for the programmed death of unwanted or damaged cells in multicellular organisms, recent structural, biochemical and cell-based assays have enhanced our understanding of the mechanisms by which some of the key proteins regulate this process. These studies have highlighted a critical role for conformational change and the regulated formation of specific complexes that can either inhibit or stimulate apoptosis. In some cases, it is still not clear what distinguishes inhibitory from activating complexes, but the value of a structural understanding is highlighted by the success of recent structure-based drug discovery programs that have targeted these complexes.

摘要

真核细胞利用复杂的信号转导蛋白网络来决定是分化、生长还是死亡。在细胞凋亡的情况下,细胞凋亡负责多细胞生物体中不需要或受损细胞的程序性死亡,最近的结构、生化和基于细胞的分析增强了我们对一些关键蛋白调节这一过程机制的理解。这些研究突出了构象变化和特定复合物的调控形成的关键作用,这些复合物可以抑制或刺激细胞凋亡。在某些情况下,仍然不清楚抑制性复合物和激活性复合物的区别是什么,但最近针对这些复合物的基于结构的药物发现项目的成功凸显了结构理解的价值。

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