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Sequence-directed concentration of G protein-coupled receptors in COPII vesicles

G protein-coupled receptors (GPCRs) constitute the largest superfamily of plasma membrane signaling proteins. However, virtually nothing is known about their recruitment to COPII vesicles for forward delivery after synthesis in the endoplasmic reticulum (ER). Here, we demonstrate that some GPCRs are...

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Detalles Bibliográficos
Autores principales: Xu, Xin, Lambert, Nevin A., Wu, Guangyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551652/
https://www.ncbi.nlm.nih.gov/pubmed/37810244
http://dx.doi.org/10.1016/j.isci.2023.107969
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author Xu, Xin
Lambert, Nevin A.
Wu, Guangyu
author_facet Xu, Xin
Lambert, Nevin A.
Wu, Guangyu
author_sort Xu, Xin
collection PubMed
description G protein-coupled receptors (GPCRs) constitute the largest superfamily of plasma membrane signaling proteins. However, virtually nothing is known about their recruitment to COPII vesicles for forward delivery after synthesis in the endoplasmic reticulum (ER). Here, we demonstrate that some GPCRs are highly concentrated at ER exit sites (ERES) before COPII budding. Angiotensin II type 2 receptor (AT2R) and CXCR4 concentration are directed by a di-acidic motif and a 9-residue domain, respectively, and these motifs also control receptor ER-Golgi traffic. We further show that AT2R interacts with Sar1 GTPase and that distinct GPCRs have different ER-Golgi transport rates via COPII which is independent of their concentration at ERES. Collectively, these data demonstrate that GPCRs can be actively captured by COPII via specific motifs and direct interaction with COPII components that in turn affects their export dynamics, and provide important insights into COPII targeting and forward trafficking of nascent GPCRs.
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spelling pubmed-105516522023-10-06 Sequence-directed concentration of G protein-coupled receptors in COPII vesicles Xu, Xin Lambert, Nevin A. Wu, Guangyu iScience Article G protein-coupled receptors (GPCRs) constitute the largest superfamily of plasma membrane signaling proteins. However, virtually nothing is known about their recruitment to COPII vesicles for forward delivery after synthesis in the endoplasmic reticulum (ER). Here, we demonstrate that some GPCRs are highly concentrated at ER exit sites (ERES) before COPII budding. Angiotensin II type 2 receptor (AT2R) and CXCR4 concentration are directed by a di-acidic motif and a 9-residue domain, respectively, and these motifs also control receptor ER-Golgi traffic. We further show that AT2R interacts with Sar1 GTPase and that distinct GPCRs have different ER-Golgi transport rates via COPII which is independent of their concentration at ERES. Collectively, these data demonstrate that GPCRs can be actively captured by COPII via specific motifs and direct interaction with COPII components that in turn affects their export dynamics, and provide important insights into COPII targeting and forward trafficking of nascent GPCRs. Elsevier 2023-09-19 /pmc/articles/PMC10551652/ /pubmed/37810244 http://dx.doi.org/10.1016/j.isci.2023.107969 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Xu, Xin
Lambert, Nevin A.
Wu, Guangyu
Sequence-directed concentration of G protein-coupled receptors in COPII vesicles
title Sequence-directed concentration of G protein-coupled receptors in COPII vesicles
title_full Sequence-directed concentration of G protein-coupled receptors in COPII vesicles
title_fullStr Sequence-directed concentration of G protein-coupled receptors in COPII vesicles
title_full_unstemmed Sequence-directed concentration of G protein-coupled receptors in COPII vesicles
title_short Sequence-directed concentration of G protein-coupled receptors in COPII vesicles
title_sort sequence-directed concentration of g protein-coupled receptors in copii vesicles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551652/
https://www.ncbi.nlm.nih.gov/pubmed/37810244
http://dx.doi.org/10.1016/j.isci.2023.107969
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