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Human substance P receptor undergoes agonist-dependent phosphorylation by G protein-coupled receptor kinase 5 in vitro
被引:3
|作者:
Warabi, K
Richardson, MD
Barry, WT
Yamaguchi, K
Roush, ED
Nishimura, K
Kwatra, MM
[1
]
机构:
[1] Duke Univ, Med Ctr, Dept Anesthesiol, Durham, NC 27710 USA
[2] Juntendo Univ, Dept Anesthesiol, Tokyo, Japan
[3] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
[4] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
关键词:
human substance P receptor;
G protein-coupled receptor kinase;
receptor phosphorylation;
desensitization;
D O I:
10.1016/S0014-5793(02)02858-2
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
G protein-coupled receptor kinases (GRKs) phosphorylate agonist-occupied G protein-coupled receptors, leading to receptor desensitization. Seven GRKs, designated GRK1 through 7, have been characterized. GRK5 is negatively regulated by protein kinase C. We investigated whether human substance P receptor (hSPR) is a substrate of GRK5. We report that membrane-bound hSPR is phosphorylated by purified GRK5, and that both the rate and extent of phosphorylation increase dramatically in the presence of substance P. The phosphorylation has a high stoichiometry (20 +/- 4 mol phosphate/mol hSPR) and a low K-m (1.7 +/- 0.1 nM). These data provide the first evidence that hSPR is a substrate of GRK5. (C)2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
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页码:140 / 144
页数:5
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