Discovery of small molecule inhibitors for the C.elegans caspase CED-3 by high-throughput screening

被引:3
作者
Brantley, Scott J. [1 ]
Cotten, Steven W. [1 ]
Lamson, David R. [2 ]
Smith, Ginger R. [2 ]
Liu, Rihe [1 ,3 ]
Williams, Kevin P. [2 ,4 ]
机构
[1] Univ N Carolina, UNC Eshelman Sch Pharm, Div Chem Biol & Med Chem, Chapel Hill, NC 27599 USA
[2] Biomfg Res Inst & Technol Enterprise, Durham, NC 27707 USA
[3] Univ N Carolina, Carolina Ctr Genome Sci, Chapel Hill, NC 27599 USA
[4] North Carolina Cent Univ, Dept Pharmaceut Sci, Chapel Hill, NC 27707 USA
基金
美国国家卫生研究院;
关键词
C.elegans; Caspase; CED-3; High-throughput screening; Small molecule inhibitor; Apoptosis; CAENORHABDITIS-ELEGANS; CELL-DEATH; C-ELEGANS; APOPTOSIS; PROTEIN; ASSAYS; SPECIFICITIES; ACTIVATION; SUBSTRATE; COMPLEX;
D O I
10.1016/j.bbrc.2017.07.100
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
C.elegans has been widely used as a model organism for programmed cell death and apoptosis. Although the CED-3 caspase is the primary effector of cell death in C.elegans, no selective inhibitors have been identified. Utilizing high-throughput screening with recombinant C.elegans CED-3 protein, we have discovered and confirmed 21 novel small molecule inhibitors. Six compounds had IC50 values < 10 mu M. From these, four distinct chemotypes were identified. The inhibitor scaffolds described here could lead to the development of selective molecular probes to facilitate our understanding of programmed cell death in this model organism. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:773 / 779
页数:7
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