Adaptation of the Ras-recruitment system to the analysis of interactions between membrane-associated proteins -: art. no. e28

被引:11
|
作者
Köhler, F [1 ]
Müller, KM [1 ]
机构
[1] Univ Freiburg, Inst Biol 3, D-79104 Freiburg, Germany
关键词
D O I
10.1093/nar/gng028
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
Interactions of membrane-associated proteins play important roles in many cellular processes. The yeast two-hybrid assay is of limited utility for the analysis of such interactions, due to the need for soluble protein partners, whose interaction is assessed in the nucleus. The advent of the Ras-recruitment system (RRS) has enabled the study of membrane-associated proteins interacting with cytoplasmic proteins fused to Ras. Constitutive membrane association of the Ras fusion protein is expected to complement the growth defect of the yeast strain CDC25-2, assayed in the RRS, independent from the interaction with a membrane-bound partner. We describe the adaptation of the RRS to the analysis of interactions between two membrane-associated proteins using a model system. These results may facilitate the study of protein-protein interactions between membrane-bound proteins and further increase the utility of the RRS.
引用
收藏
页数:4
相关论文
empty
未找到相关数据