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The regulators of G protein signaling RGS16 and RGS18 inhibit protease‐activated receptor 2/Gi/o signaling through distinct interactions with Gα in live cells.

Authors :
Kim, Kiman
Lee, Jinyong
Ghil, Sungho
Source :
FEBS Letters. Sep2018, Vol. 592 Issue 18, p3126-3138. 13p.
Publication Year :
2018

Abstract

Protease‐activated receptor 2 (PAR2) is a G protein‐coupled receptor (GPCR) activated by endogenous proteases, in particular, trypsin. Although regulators of G protein signaling (RGS) are known to inhibit GPCR/Gα‐mediated signaling, their specific effects on PAR2 are poorly understood at present. Here, we use a bioluminescence resonance energy transfer technique to investigate whether RGS16 and RGS18 bind PAR2 in live cells to regulate PAR2/Gαi/o‐mediated signaling. Notably, we find that RGS16 binds to PAR2 in the presence of Gαi while RGS18 does not interact with PAR2, regardless of the presence of Gα. Both RGS16 and RGS18 inhibit PAR2/Gαi/o‐mediated signaling. To our knowledge, the current study is the first to highlight the effects of RGS proteins on PAR2‐mediated signaling. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00145793
Volume :
592
Issue :
18
Database :
Academic Search Index
Journal :
FEBS Letters
Publication Type :
Academic Journal
Accession number :
131949022
Full Text :
https://doi.org/10.1002/1873-3468.13220