Year: 2003
Type: article
Abstract: 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.
Source: Cell Communication & Adhesion
DOI: 10.1080/714040428
Language: English
Topic: Connexins and lens biology
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: bronze
Awards: A gap junction-independent role for Connexin43 in cardiac electrophysiology, G2264610468, G2575637574, Molecular Neuropathology, G3508417182, Intercellular Communication and Impulse Propagation, The Astrocyte Nexus: CX43-Protein Interactions, G5988442279, GAP JUNCTIONS AND SCHWANN CELLS, G882646002, G9000080889
OpenAlex ID: W2027536289