Cargando…
A synthetic intrabody based selective and generic inhibitor of GPCR endocytosis
β-arrestins (βarrs) critically mediate desensitization, endocytosis and signaling of G Protein-Coupled Receptors (GPCRs), and they scaffold a large number of interaction partners. However, allosteric modulation of their scaffolding abilities and direct targeting of their interaction interfaces to se...
Autores principales: | Ghosh, Eshan, Srivastava, Ashish, Baidya, Mithu, Kumari, Punita, Dwivedi, Hemlata, Nidhi, Kumari, Ranjan, Ravi, Dogra, Shalini, Koide, Akiko, Yadav, Prem N., Sidhu, Sachdev S., Koide, Shohei, Shukla, Arun K. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5722207/ https://www.ncbi.nlm.nih.gov/pubmed/28967893 http://dx.doi.org/10.1038/nnano.2017.188 |
Ejemplares similares
-
Allosteric modulation of GPCR-induced β-arrestin trafficking and signaling by a synthetic intrabody
por: Baidya, Mithu, et al.
Publicado: (2022) -
Core engagement with β-arrestin is dispensable for agonist-induced vasopressin receptor endocytosis and ERK activation
por: Kumari, Punita, et al.
Publicado: (2017) -
Functional competence of a partially engaged GPCR–β-arrestin complex
por: Kumari, Punita, et al.
Publicado: (2016) -
Distinct phosphorylation sites in a prototypical GPCR differently orchestrate β-arrestin interaction, trafficking, and signaling
por: Dwivedi-Agnihotri, Hemlata, et al.
Publicado: (2020) -
Selective targeting of ligand-dependent and -independent signaling by GPCR conformation-specific anti-US28 intrabodies
por: De Groof, Timo W. M., et al.
Publicado: (2021)