BAX, BAK, and BOK: A Coming of Age for the BCL-2 Family Effector Proteins

被引:157
作者
Moldoveanu, Tudor [1 ,2 ]
Czabotar, Peter E. [3 ,4 ]
机构
[1] St Jude Childrens Res Hosp, Dept Struct Biol, 332 N Lauderdale St, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Chem Biol & Therapeut, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] Univ Melbourne, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3052, Australia
[4] Univ Melbourne, Dept Med Biol, Parkville, Vic 3010, Australia
关键词
MEMBER BOK; MEMBRANE PERMEABILIZATION; MITOCHONDRIAL BAX; PORE FORMATION; BH3; DOMAINS; CELL-DEATH; BH3-ONLY PROTEINS; DIRECT ACTIVATION; APOPTOTIC BAX; OLIGOMERIZATION;
D O I
10.1101/cshperspect.a036319
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The BCL-2 family of proteins control a key checkpoint in apoptosis, that of mitochondrial outer membrane permeabilization or, simply, mitochondria! poration. The family consists of three subgroups: BH3-only initiators that respond to apoptotic stimuli; antiapoptotic guardians that protect against cell death; and the membrane permeabilizing effectors BAX, BAK, and BOK. On activation, effector proteins are converted from inert monomers into membrane permeabilizing oligomers. For many years, this process has been poorly understood at the molecular level, but a number of recent advances have provided important insights. We review the regulation of these effectors, their activation, subsequent conformational changes, and the ensuing oligomerization events that enable mitochondrial poration, which initiates apoptosis through release of key signaling factors such as cytochrome c. We highlight the mysteries that remain in understanding these important proteins in an endeavor to provide a comprehensive picture of where the field currently sits and where it is moving toward.
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页数:19
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