Cloning of ligand targets: Systematic isolation of SH3 domain-containing proteins

被引:213
作者
Sparks, AB
Hoffman, NG
McConnell, SJ
Fowlkes, DM
Kay, BK
机构
[1] UNIV N CAROLINA, DEPT BIOL, CURRICULUM GENET & MOL BIOL, CHAPEL HILL, NC 27599 USA
[2] UNIV N CAROLINA, DEPT PATHOL, CHAPEL HILL, NC 27599 USA
[3] UNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USA
[4] CYTOGEN CORP, PRINCETON, NJ 08540 USA
关键词
Src homology domain; genomics; signal transduction;
D O I
10.1038/nbt0696-741
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Based on the prevalence of modular protein domains, such as Src homology domain 3 and 2 (SH3 and SH2), among important signaling molecules, we have sought to identify new SH3 domain-containing proteins. However, modest sequence similarity among these domains restricts the use of DNA-based methods for this purpose. To circumvent this limitation, we have developed a functional screen that permits the rapid cloning of modular domains based on their ligand-binding activity. Using operationally defined SH3 ligands from combinatorial peptide libraries, we screened a series of mouse and human cDNA expression libraries. We found that 69 of the 74 clones isolated encode at least one SH3 domain. These clones encode 18 different SH3-containing proteins, in of which have not been described previously. The isolation of entire repertoires of modular domain-containing proteins will prove invaluable in genome analysis and in bringing new targets into drug discovery programs.
引用
收藏
页码:741 / 744
页数:4
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