Targeting apoptosis via chemical design: Inhibition of bid-induced cell death by small organic molecules

被引:79
作者
Becattini, B [1 ]
Sareth, S [1 ]
Zhai, DY [1 ]
Crowell, KJ [1 ]
Leone, M [1 ]
Reed, JC [1 ]
Pellecchia, M [1 ]
机构
[1] Burnham Inst, La Jolla, CA 92037 USA
来源
CHEMISTRY & BIOLOGY | 2004年 / 11卷 / 08期
关键词
D O I
10.1016/j.chembiol.2004.05.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bid is a key member of the Bcl-2 family proteins involved in the control of the apoptotic cascade in cells, leading to cell death. Uncontrolled cell death is associated with several human pathologies, such as neurodegenerative diseases and ischemic injuries. Therefore, Bid represents a potential yet unexplored and challenging target for strategies aimed at the development of therapeutic agents. Here we show that a multidisciplinary NMR-based approach that we named SAR by ILOEs (structure activity relationships by interligand nuclear Overhauser effect) allowed us to rationally design a series of 4-phenylsulfanyl-phenylamine derivatives that are capable of occupying a deep hydrophobic crevice on the surface of Bid. These compounds represent the first antiapoptotic small molecules targeting a Bcl-2 protein as shown by their ability to inhibit tBid-induced SMAC release, caspase-3 activation, and cell death.
引用
收藏
页码:1107 / 1117
页数:11
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