Immunoprecipitation techniques for the analysis of transcription factor complexes

被引:51
作者
Klenova, E [1 ]
Chernukhin, I [1 ]
Inoue, T [1 ]
Shamsuddin, S [1 ]
Norton, J [1 ]
机构
[1] Univ Essex, Gene Regulat Lab, Dept Biol Sci, Colchester CO4 3SQ, Essex, England
关键词
immunoprecipitation; transcription factor; Id3 helix-loop-helix protein; Pax5/CTCF;
D O I
10.1016/S1046-2023(02)00029-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Interactions among transcription factors can be detected and analyzed by a variety of in vitro and in vivo approaches. In many studies, the existence of putative interactions among transcription factor partners is initially established from yeast two-hybrid screening and in vitro protein association analysis. The ability to detect candidate interacting proteins in coimmunoprecipitates from cell lysates provides an important criterion for establishing the authenticity of such protein interactions in vivo. This article describes methodology developed for detecting interactions between the helix-loop-helix protein, Id3, and the paired homeodomain protein, Pax5, and interactions involving the zinc finger transcription factor, CTCF. The importance of empirically establishing optimum conditions for cell lysis, selection of appropriate antibodies, conditions for immunoprecipitation, and detection of interacting partners are discussed. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:254 / 259
页数:6
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