Osborne M A, Dalton S, Kochan J P
Department of Inflammation/Autoimmune Diseases, Hoffmann-La Roche, Inc., USA.
Biotechnology (N Y). 1995 Dec;13(13):1474-8. doi: 10.1038/nbt1295-1474.
Protein-protein interactions are often dependent on the post-translational modification of one component of a complex. To facilitate the study of these interactions in signal transduction, we have developed the yeast tribrid system, a modification of the yeast two-hybrid system. We demonstrate that the interactions are dependent upon the presence of a tyrosine kinase, an SH2 domain and a tyrosine containing substrate. Using the gamma subunit of the high-affinity IgE receptor, Fc epsilon RI, this approach has been used to isolate a novel SH2-containing family member. The mRNA encoding this novel protein is differentially expressed in rat tissues. The yeast tribrid system can be readily adapted for the characterization of novel tyrosine kinases or substrates, as well as the study of protein-protein interactions which involve other post-translational modifications.
蛋白质-蛋白质相互作用通常依赖于复合物中一个组分的翻译后修饰。为便于研究信号转导中的这些相互作用,我们开发了酵母三杂交系统,它是酵母双杂交系统的一种改良形式。我们证明这些相互作用依赖于酪氨酸激酶、SH2结构域和含酪氨酸底物的存在。利用高亲和力IgE受体FcεRI的γ亚基,该方法已用于分离一个新的含SH2结构域家族成员。编码这种新蛋白质的mRNA在大鼠组织中差异表达。酵母三杂交系统可很容易地用于鉴定新的酪氨酸激酶或底物,以及研究涉及其他翻译后修饰的蛋白质-蛋白质相互作用。