共 95 条
Identifying small molecule inhibitors of eukaryotic translation initiation
被引:15
作者:

Cencic, Regina
论文数: 0 引用数: 0
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机构:
McGill Univ, Dept Biochem, Montreal, PQ, Canada McGill Univ, Dept Biochem, Montreal, PQ, Canada

Robert, Francis
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h-index: 0
机构: McGill Univ, Dept Biochem, Montreal, PQ, Canada

Pelletier, Jerry
论文数: 0 引用数: 0
h-index: 0
机构: McGill Univ, Dept Biochem, Montreal, PQ, Canada
机构:
[1] McGill Univ, Dept Biochem, Montreal, PQ, Canada
[2] McGill Univ, McGill Canc Ctr, Montreal, PQ, Canada
来源:
TRANSLATION INITIATION: CELL BIOLOGY, HIGH-THROUGHPUT METHODS, AND CHEMICAL-BASED APPROACHES
|
2007年
/
431卷
关键词:
D O I:
10.1016/S0076-6879(07)31013-6
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
In eukaryotes, translation initiation is rate-limiting with much regulation exerted at the ribosome recruitment and ternary complex (eIF2 center dot GTP center dot Met-tRNA(i)(Met)) formation steps. Although small molecule inhibitors have been extremely useful for chemically dissecting translation, there is a dearth of compounds available to study the initiation phase in vitro and in vivo. In this chapter, we describe reverse and forward chemical genetic screens developed to identify new inhibitors of translation. The ability to manipulate cell extracts biochemically, and to compare the activity of small molecules on translation of mRNA templates that differ in their factor requirements for ribosome recruitment, facilitates identification of the relevant target.
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页码:269 / 302
页数:34
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共 95 条
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