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Direct visualization of single-molecule membrane protein interactions in living cells

Interactions between membrane proteins are poorly understood despite their importance in cell signaling and drug development. Here, we present a co-immunoimmobilization assay (Co-II) enabling the direct observation of membrane protein interactions in single living cells that overcomes the limitation...

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Detalles Bibliográficos
Autores principales: Kim, Do-Hyeon, Park, Soyeon, Kim, Dong-Kyun, Jeong, Min Gyu, Noh, Jungeun, Kwon, Yonghoon, Zhou, Kai, Lee, Nam Ki, Ryu, Sung Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307816/
https://www.ncbi.nlm.nih.gov/pubmed/30543635
http://dx.doi.org/10.1371/journal.pbio.2006660
Descripción
Sumario:Interactions between membrane proteins are poorly understood despite their importance in cell signaling and drug development. Here, we present a co-immunoimmobilization assay (Co-II) enabling the direct observation of membrane protein interactions in single living cells that overcomes the limitations of currently prevalent proximity-based indirect methods. Using Co-II, we investigated the transient homodimerizations of epidermal growth factor receptor (EGFR) and beta-2 adrenergic receptor (β2-AR) in living cells, revealing the differential regulation of these receptors’ dimerizations by molecular conformations and microenvironment in a plasma membrane. Co-II should provide a simple, rapid, and robust platform for visualizing both weak and strong protein interactions in the plasma membrane of living cells.