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Blot overlays with 32P-labeled fusion proteins.

机译:用32P标记的融合蛋白印迹覆盖图。

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Proteins labeled with 32P can be used as sensitive "prime" in blot overlays to detect binding proteins or domains. Small G-protein Ras can bind GTP with extremely high affinity (Kd approximately 10(-11)-10(-12) M) in the presence of Mg2+. We have taken advantage of this property of Ras to develop a vector that expresses proteins of interest such as glutathione S-transferase (GST)/Ras fusion proteins for noncovalent labeling with [gamma-32P]GTP. The labeling efficiency of this method is >60% and involves a single short incubation step. We have previously identified several binding proteins for the second SH3 domain of the adaptor Nck using this method. Here we illustrate the overlay method using the GST/Ras system and compare results with the SH3 domain labeled by phosphorylation with [gamma-32P]ATP. Both methods are similarly specific and sensitive; however, we show that signals are dependent primarily on GST-mediated probe dimerization. These dimeric probes allow a more stable probe-target complex similar to immunoglobulin interactions, thus significantly improving the sensitivity of the technique. Copyright 2001 Academic Press.
机译:标记为32P的蛋白可用作印迹覆盖图中的敏感“底漆”,以检测结合蛋白或结构域。在Mg2 +存在下,小G蛋白Ras可以以极高的亲和力(Kd约为10(-11)-10(-12)M)结合GTP。我们已经利用Ras的这种特性来开发一种载体,该载体表达感兴趣的蛋白质,例如谷胱甘肽S-转移酶(GST)/ Ras融合蛋白,用于用[γ-32P] GTP进行非共价标记。此方法的标记效率> 60%,涉及一个短的孵育步骤。我们以前已经使用这种方法为衔接子Nck的第二个SH3域鉴定了几种结合蛋白。在这里,我们说明了使用GST / Ras系统的叠加方法,并将结果与​​通过[γ-32P] ATP磷酸化标记的SH3域进行了比较。两种方法都具有相似的特异性和敏感性。但是,我们显示信号主要取决于GST介导的探针二聚化。这些二聚体探针允许类似于免疫球蛋白相互作用的更稳定的探针-靶复合物,从而显着提高了该技术的灵敏度。版权所有2001,学术出版社。

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