Genetic approaches to the identification of interactions between membrane proteins in yeast

被引:9
作者
Auerbach, D
Galeuchet-Schenk, B
Hottiger, MO
Stagljar, I
机构
[1] DUALSYST BIOTECH Inc, CH-8057 Zurich, Switzerland
[2] Univ Zurich Irchel, Inst Vet Biochem & Mol Biol, CH-8057 Zurich, Switzerland
来源
JOURNAL OF RECEPTOR AND SIGNAL TRANSDUCTION RESEARCH | 2002年 / 22卷 / 1-4期
关键词
yeast two-hybrid; split-ubiquitin; protein-protein interactions; integral membrane proteins; high-throughput screening;
D O I
10.1081/RRS-120014615
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
The recent sequencing of entire eukaryotic genomes has renewed the interest in identifying and characterizing all gene products that are expressed in a given organism. The characterization of unknown gene products is facilitated by. the knowledge of its binding partners. Thus, a novel protein may be classified by identifying previously characterized proteins that interact with it. If such an approach is carried out on a large scale, it may allow the rapid characterization of the thousands of predicted open reading frames identified by recent sequencing projects. Currently, the yeast two-hybrid system is the most widely used genetic assay for the detection of protein-protein interactions. The yeast two-hybrid system has become popular because it requires little individual optimization and because, as compared to conventional biochemical methods, the identification and characterization of protein-protein interactions can be completed in a relatively short time span. In this review, we briefly discuss the yeast two-hybrid system and its application to large scale screening studies that aim at deciphering all protein-protein interactions taking place in a given cell type or organism. We then focus on a class of proteins that is unsuitable for conventional yeast two-hybrid systems, namely integral membrane proteins and membrane-associated proteins, and describe several novel genetic systems that combine the advantages of the yeast two-hybrid system with the potential to identify interaction partners of membrane-associated proteins in their natural setting.
引用
收藏
页码:471 / 481
页数:11
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