Results 41 to 50 of about 17,943 (269)

Quantification of beta adrenergic receptor subtypes in beta-arrestin knockout mouse airways. [PDF]

open access: yesPLoS ONE, 2015
In allergic asthma Beta 2 adrenergic receptors (β2ARs) are important mediators of bronchorelaxation and, paradoxically, asthma development. This contradiction is likely due to the activation of dual signaling pathways that are downstream of G proteins or
Akhil Hegde   +2 more
doaj   +1 more source

Endocrinology and the brain: Corticotropin-Releasing Hormone signaling [PDF]

open access: yes, 2017
Corticotropin-releasing hormone (CRH) is a key player of basal and stress activated responses in the hypothalamic-pituitary-adrenal axis (HPA) and in extrahypothalamic circuits, where it functions as a neuromodulator to orchestrate humoral and behavioral
Armando, Natalia Giannina   +3 more
core   +2 more sources

Arrestins: structural disorder creates rich functionality

open access: yesProtein & Cell, 2018
Arrestins are soluble relatively small 44–46 kDa proteins that specifically bind hundreds of active phosphorylated GPCRs and dozens of non-receptor partners.
Vsevolod V. Gurevich   +2 more
doaj   +1 more source

Ubiquitin Ligase Parkin Promotes Mdm2–Arrestin Interaction but Inhibits Arrestin Ubiquitination [PDF]

open access: yesBiochemistry, 2011
Numerous mutations in E3 ubiquitin ligase parkin were shown to associate with familial Parkinson's disease. Here we show that parkin binds arrestins, versatile regulators of cell signaling. Arrestin-parkin interaction was demonstrated by coimmunoprecipitation of endogenous proteins from brain tissue and shown to be direct using purified proteins ...
M Rafiuddin, Ahmed   +5 more
openaire   +2 more sources

Identification and light-dependent translocation of a cone-specific antigen, cone arrestin, recognized by monoclonal antibody 7G6 [PDF]

open access: yes, 2003
PURPOSE: To elucidate the antigen recognized by monoclonal antibody (mAb) 7G6, a widely used cone-specific marker. METHODS: 7G6 immunocytochemistry was performed on sections of human, primate, and bovine retina.
Baehr, Wolfgang   +6 more
core   +2 more sources

To Be Biased or Not to Be: A Play for G-Protein Coupled Receptors

open access: yesInternational Journal of Translational Medicine
G protein-coupled receptors (GPCRs) are the largest family of diverse receptors in eukaryotic organisms, playing a critical role in modulating human physiology. It therefore comes as no surprise that about 36% of all currently available drugs target this
Nikitas G. Liolitsas   +2 more
doaj   +1 more source

Lack of beta-arrestin signaling in the absence of active G proteins

open access: yesNature Communications, 2018
Arrestins terminate signaling from GPCRs, but several lines of evidence suggest that they are also able to transduce signals independently of G proteins. Here, the authors systematically ablate G proteins in cell lines, and show that arrestins are unable
Manuel Grundmann   +23 more
doaj   +1 more source

Reduced expression of G protein-coupled receptor kinases in schizophrenia but not in schizoaffective disorder

open access: yesNeurobiology of Disease, 2011
Alterations of multiple G protein-mediated signaling pathways are detected in schizophrenia. G protein-coupled receptor kinases (GRKs) and arrestins terminate signaling by G protein-coupled receptors exerting a powerful influence on receptor functions ...
E.R. Bychkov   +4 more
doaj   +1 more source

β-Arrestin regulation of myosin light chain phosphorylation promotes AT1aR-mediated cell contraction and migration. [PDF]

open access: yesPLoS ONE, 2013
Over the last decade, it has been established that G-protein-coupled receptors (GPCRs) signal not only through canonical G-protein-mediated mechanisms, but also through the ubiquitous cellular scaffolds β-arrestin-1 and β-arrestin-2.
Elie Simard   +5 more
doaj   +1 more source

Discrete GPCR-triggered endocytic modes enable β-arrestins to flexibly regulate cell signaling

open access: yeseLife, 2022
β-Arrestins are master regulators of cellular signaling that operate by desensitizing ligand-activated G-protein-coupled receptors (GPCRs) at the plasma membrane and promoting their subsequent endocytosis.
Benjamin Barsi-Rhyne   +2 more
doaj   +1 more source

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