Computer-aided design of a PDZ domain to recognize new target sequences

被引:128
作者
Reina, J
Lacroix, E
Hobson, SD
Fernandez-Ballester, G
Rybin, V
Schwab, MS
Serrano, L
Gonzalez, C [1 ]
机构
[1] European Mol Biol Lab, Cell Biol & Biophys Program, D-69117 Heidelberg, Germany
[2] European Mol Biol Lab, Struct Biol & Biocomp Program, D-69117 Heidelberg, Germany
[3] CellZome AG, D-69117 Heidelberg, Germany
关键词
D O I
10.1038/nsb815
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
PDZ domains are small globular domains that recognize the last 4-7 amino acids at the C-terminus of target proteins. The specificity of the PDZ-ligand recognition is due to side chain-side chain interactions, as well as the positioning of an a-helix involved in ligand binding. We have used computer-aided protein design to produce mutant versions of a Class I PDZ domain that bind to novel Class I and Class 11 target sequences both in vitro and in vivo, thus providing an alternative to primary antibodies in western blotting, affinity chromatography and pull-down experiments. Our results suggest that by combining different backbone templates with computer-aided protein design, PDZ domains could be engineered to specifically recognize a large number of proteins.
引用
收藏
页码:621 / 627
页数:7
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