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Kinetics of Protein-Protein Interactions of Connexins: Use of Enzyme Linked Sorbent Assays

机译:连接蛋白的蛋白质-蛋白质相互作用的动力学:酶联吸附法的使用

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Determination of the protein-protein interactions of connexins has become a rapidly expanding field of research. While there are multiple methods of determining the identity of binding partners, determination of the strengths of interactions is not as simple. Here we describe the use of the in vitro method Enzyme Linked Sorbent Assay (ELSA) to compare binding affinities of known protein partners for Connexin43. We used the binding of Cx43 Carboxyl Terminal domain to the PDZ-2 domain of Zonula Occludens-1 and to the SH3 domain of c-Src. In the ELSA assay we found that while the binding of the SH3 domain of c-Src is pH-dependent, the interaction of the PDZ domain of ZO-1 is not. These data confirm findings using Surface Plasmon Resonance (1) and indicate that ELSA can be a useful tool in determining the kinetics of protein-protein interactions.
机译:连接蛋白的蛋白质-蛋白质相互作用的测定已经成为快速发展的研究领域。尽管有多种确定结合伴侣身份的方法,但确定相互作用强度的方法却并非如此简单。在这里,我们描述了使用体外方法酶联吸附法(ELSA)来比较已知蛋白伴侣对Connexin43的结合亲和力。我们使用了Cx43羧基末端域与Zonula Occludens-1的PDZ-2域和c-Src的SH3域的结合。在ELSA分析中,我们发现虽然c-Src的SH3结构域的结合是pH依赖性的,但ZO-1的PDZ结构域的相互作用却不依赖于pH。这些数据证实了使用表面等离振子共振的发现(1),并表明ELSA可能是确定蛋白质相互作用的动力学的有用工具。

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