Jak Grimes
Plasma membrane preassociation drives β-arrestin coupling to receptors and activation
Grimes, Jak; Koszegi, Zsombor; Lanoiselée, Yann; Miljus, Tamara; O’Brien, Shannon L.; Stepniewski, Tomasz M.; Medel-Lacruz, Brian; Baidya, Mithu; Makarova, Maria; Mistry, Ravi; Goulding, Joëlle; Drube, Julia; Hoffmann, Carsten; Owen, Dylan M.; Shukla, Arun K.; Selent, Jana; Hill, Stephen J.; Calebiro, Davide
Authors
Zsombor Koszegi
Yann Lanoiselée
Tamara Miljus
Shannon L. O’Brien
Tomasz M. Stepniewski
Brian Medel-Lacruz
Mithu Baidya
Maria Makarova
Ravi Mistry
JOELLE GOULDING JOELLE.GOULDING@NOTTINGHAM.AC.UK
Senior Research Fellow
Julia Drube
Carsten Hoffmann
Dylan M. Owen
Arun K. Shukla
Jana Selent
STEPHEN HILL STEVE.HILL@NOTTINGHAM.AC.UK
Professor of Molecular Pharmacology
Davide Calebiro
Abstract
β-arrestin plays a key role in G protein-coupled receptor (GPCR) signaling and desensitization. Despite recent structural advances, the mechanisms that govern receptor-β-arrestin interactions at the plasma membrane of living cells remain elusive. Here, we combine single-molecule microscopy with molecular dynamics simulations to dissect the complex sequence of events involved in β-arrestin interactions with both receptors and the lipid bilayer. Unexpectedly, our results reveal that β-arrestin spontaneously inserts into the lipid bilayer and transiently interacts with receptors via lateral diffusion on the plasma membrane. Moreover, they indicate that, following receptor interaction, the plasma membrane stabilizes β-arrestin in a longer-lived, membrane-bound state, allowing it to diffuse to clathrin-coated pits separately from the activating receptor. These results expand our current understanding of β-arrestin function at the plasma membrane, revealing a critical role for β-arrestin preassociation with the lipid bilayer in facilitating its interactions with receptors and subsequent activation.
Citation
Grimes, J., Koszegi, Z., Lanoiselée, Y., Miljus, T., O’Brien, S. L., Stepniewski, T. M., Medel-Lacruz, B., Baidya, M., Makarova, M., Mistry, R., Goulding, J., Drube, J., Hoffmann, C., Owen, D. M., Shukla, A. K., Selent, J., Hill, S. J., & Calebiro, D. (2023). Plasma membrane preassociation drives β-arrestin coupling to receptors and activation. Cell, 186(10), 2238-2255. https://doi.org/10.1016/j.cell.2023.04.018
Journal Article Type | Article |
---|---|
Acceptance Date | Apr 12, 2023 |
Online Publication Date | May 4, 2023 |
Publication Date | May 11, 2023 |
Deposit Date | May 5, 2023 |
Publicly Available Date | May 10, 2023 |
Journal | Cell |
Print ISSN | 0092-8674 |
Electronic ISSN | 1097-4172 |
Publisher | Cell Press |
Peer Reviewed | Peer Reviewed |
Volume | 186 |
Issue | 10 |
Pages | 2238-2255 |
DOI | https://doi.org/10.1016/j.cell.2023.04.018 |
Keywords | G protein-coupled receptors; GPCR; arrestin; single-molecule microscopy; TIRF; protein-protein interactions; plasma membrane |
Public URL | https://nottingham-repository.worktribe.com/output/20285228 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S0092867423004142 |
Files
1-s2.0-S0092867423004142-main
(11 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
You might also like
The tetraspanin Tspan15 is an essential subunit of an ADAM10 scissor complex
(2020)
Journal Article
Detection of genome-edited and endogenously expressed G protein-coupled receptors
(2021)
Journal Article
Downloadable Citations
About Repository@Nottingham
Administrator e-mail: discovery-access-systems@nottingham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search