The biochemical mechanism of Rho GTPase membrane binding, activation and retention in activity patterning

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Title: The biochemical mechanism of Rho GTPase membrane binding, activation and retention in activity patterning
Authors: Michael C Armstrong, Yannic R Weiß, Lila E Hoachlander-Hobby, Ankit A Roy, Ilaria Visco, Alison Moe, Adriana E Golding, Scott D Hansen, William M Bement, Peter Bieling
Source: EMBO J
Armstrong, M C, Weiß, Y R, Hoachlander-Hobby, L E, Roy, A A, Visco, I, Moe, A, Golding, A E, Hansen, S D, Bement, W M & Bieling, P 2025, ' The biochemical mechanism of Rho GTPase membrane binding, activation and retention in activity patterning ', The EMBO journal, vol. 44, no. 9, 71, pp. 2620-2657 . https://doi.org/10.1038/s44318-025-00418-z
Publisher Information: Springer Science and Business Media LLC, 2025.
Publication Year: 2025
Subject Terms: Guanine Nucleotide Exchange Factors/metabolism, rho GTP-Binding Proteins, Cell Membrane/metabolism, Cell Membrane, GTPase-Activating Proteins, GTPase-Activating Proteins/metabolism, Guanine Nucleotide Dissociation Inhibitors/metabolism, Article, Enzyme Activation, rho GTP-Binding Proteins/metabolism, Guanine Nucleotide Exchange Factors, Humans, Animals, Protein Binding, Guanine Nucleotide Dissociation Inhibitors
Description: Rho GTPases form plasma membrane-associated patterns that control the cytoskeleton during cell division, morphogenesis, migration, and wound repair. Their patterning involves transitions between inactive cytosolic and active membrane-bound states, regulated by guanine nucleotide exchange factors (GEFs), GTPase-activating proteins (GAPs), and guanine nucleotide dissociation inhibitors (GDIs). However, the relationships between these transitions and role of different regulators remain unclear. We developed a novel reconstitution approach to study Rho GTPase patterning with all major GTPase regulators in a biochemically defined system. We show that Rho GTPase dissociation from RhoGDI is rate-limiting for its membrane association. Rho GTPase activation occurs after membrane insertion, which is unaffected by GEF activity. Once activated, Rho GTPases are retained at the membrane through effector interactions, essential for their enrichment at activation sites. Thus, high cytosolic levels of RhoGDI-bound GTPases ensure a constant supply of inactive GTPases for the membrane, where GEF-mediated activation and effector binding stabilize them. These results delineate the route by which Rho GTPase patterns are established and define stage-dependent roles of its regulators.
Document Type: Article
Other literature type
File Description: application/pdf
Language: English
ISSN: 1460-2075
DOI: 10.1038/s44318-025-00418-z
Access URL: https://pubmed.ncbi.nlm.nih.gov/40164947
https://kclpure.kcl.ac.uk/ws/files/344447849/armstrong-et-al-the-biochemical-mechanism-of-rho-gtpase-membrane-binding-activation-and-retention-in-activity-patterning.pdf
Rights: CC BY
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Accession Number: edsair.doi.dedup.....2e33a06f37be1b24c1ca4806a5afd22c
Database: OpenAIRE
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