TY - JOUR
T1 - Profiling the proximal proteome of the activated μ-opioid receptor
AU - Polacco, Benjamin J.
AU - Lobingier, Braden T.
AU - Blythe, Emily E.
AU - Abreu, Nohely
AU - Khare, Prachi
AU - Howard, Matthew K.
AU - Gonzalez-Hernandez, Alberto J.
AU - Xu, Jiewei
AU - Li, Qiongyu
AU - Novy, Brandon
AU - Naing, Zun Zar Chi
AU - Shoichet, Brian K.
AU - Coyote-Maestas, Willow
AU - Levitz, Joshua
AU - Krogan, Nevan J.
AU - Von Zastrow, Mark
AU - Hüttenhain, Ruth
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature America, Inc. 2024.
PY - 2024
Y1 - 2024
N2 - The μ-opioid receptor (μOR) represents an important target of therapeutic and abused drugs. So far, most understanding of μOR activity has focused on a subset of known signal transducers and regulatory molecules. Yet μOR signaling is coordinated by additional proteins in the interaction network of the activated receptor, which have largely remained invisible given the lack of technologies to interrogate these networks systematically. Here we describe a proteomics and computational approach to map the proximal proteome of the activated μOR and to extract subcellular location, trafficking and functional partners of G-protein-coupled receptor (GPCR) activity. We demonstrate that distinct opioid agonists exert differences in the μOR proximal proteome mediated by endocytosis and endosomal sorting. Moreover, we identify two new μOR network components, EYA4 and KCTD12, which are recruited on the basis of receptor-triggered G-protein activation and might form a previously unrecognized buffering system for G-protein activity broadly modulating cellular GPCR signaling. (Figure presented.)
AB - The μ-opioid receptor (μOR) represents an important target of therapeutic and abused drugs. So far, most understanding of μOR activity has focused on a subset of known signal transducers and regulatory molecules. Yet μOR signaling is coordinated by additional proteins in the interaction network of the activated receptor, which have largely remained invisible given the lack of technologies to interrogate these networks systematically. Here we describe a proteomics and computational approach to map the proximal proteome of the activated μOR and to extract subcellular location, trafficking and functional partners of G-protein-coupled receptor (GPCR) activity. We demonstrate that distinct opioid agonists exert differences in the μOR proximal proteome mediated by endocytosis and endosomal sorting. Moreover, we identify two new μOR network components, EYA4 and KCTD12, which are recruited on the basis of receptor-triggered G-protein activation and might form a previously unrecognized buffering system for G-protein activity broadly modulating cellular GPCR signaling. (Figure presented.)
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U2 - 10.1038/s41589-024-01588-3
DO - 10.1038/s41589-024-01588-3
M3 - Article
AN - SCOPUS:85188520960
SN - 1552-4450
JO - Nature Chemical Biology
JF - Nature Chemical Biology
ER -