βArrestins in Cardiac G Protein-Coupled Receptor Signaling and Function: Partners in Crime or “Good Cop, Bad Cop”?
βarrestin (βarr)-1 and -2 (βarrs) (or Arrestin-2 and -3, respectively) are universal G protein-coupled receptor (GPCR) adapter proteins expressed abundantly in extra-retinal tissues, including the myocardium. Both were discovered in the lab of the 2012 Nobel Prize in Chemistry co-laureate Robert Lef...
Main Authors: | Anastasios Lymperopoulos, Shmuel Negussie |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2013-12-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | http://www.mdpi.com/1422-0067/14/12/24726 |
Similar Items
-
New Insights into Arrestin Recruitment to GPCRs
by: Martin Spillmann, et al.
Published: (2020-07-01) -
The Role of β-Arrestin Proteins in Organization of Signaling and Regulation of the AT1 Angiotensin Receptor
by: Gábor Turu, et al.
Published: (2019-08-01) -
Asymmetric Recruitment of β-Arrestin1/2 by the Angiotensin II Type I and Prostaglandin F2α Receptor Dimer
by: Dany Fillion, et al.
Published: (2019-03-01) -
Beta-Arrestins in the Treatment of Heart Failure Related to Hypertension: A Comprehensive Review
by: Ahmed Rakib, et al.
Published: (2021-06-01) -
Epigallocatechin Gallate Attenuated the Activation of Rat Cardiac Fibroblasts Induced by Angiotensin II via Regulating β-Arrestin1
by: Yong-Sheng Han, et al.
Published: (2013-03-01)