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线粒体作为促凋亡蛋白Bax的作用靶点。

Mitochondria as the target of the pro-apoptotic protein Bax.

作者信息

Er Emine, Oliver Lisa, Cartron Pierre-François, Juin Philippe, Manon Stephen, Vallette François M

机构信息

UMR 601 INSERM, Université de Nantes, 9 Quai Moncousu F-44035 Nantes, Cedex 01 France.

出版信息

Biochim Biophys Acta. 2006 Sep-Oct;1757(9-10):1301-11. doi: 10.1016/j.bbabio.2006.05.032. Epub 2006 May 27.

Abstract

During apoptosis, engagement of the mitochondrial pathway involves the permeabilization of the outer mitochondrial membrane (OMM), which leads to the release of cytochrome c and other apoptogenic proteins such as Smac/DIABLO, AIF, EndoG, Omi/HtraA2 and DDP/TIMM8a. OMM permeabilization depends on activation, translocation and oligomerization of multidomain Bcl-2 family proteins such as Bax or Bak. Factors involved in Bax conformational change and the function(s) of the distinct domains controlling the addressing and the insertion of Bax into mitochondria are described in this review. We also discuss our current knowledge on Bax oligomerization and on the molecular mechanisms underlying the different models accounting for OMM permeabilization during apoptosis.

摘要

在细胞凋亡过程中,线粒体途径的激活涉及线粒体外膜(OMM)的通透性改变,这会导致细胞色素c和其他凋亡蛋白的释放,如Smac/DIABLO、AIF、EndoG、Omi/HtraA2和DDP/TIMM8a。OMM通透性改变取决于多结构域Bcl-2家族蛋白(如Bax或Bak)的激活、易位和寡聚化。本综述描述了参与Bax构象变化的因素以及控制Bax靶向定位和插入线粒体的不同结构域的功能。我们还讨论了目前关于Bax寡聚化以及凋亡过程中OMM通透性改变的不同模型背后分子机制的认识。

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