Peptide substrates for G protein-coupled receptor kinase 2

被引:14
作者
Asai, Daisuke [1 ]
Toita, Riki [2 ]
Murata, Masaharu [3 ]
Katayama, Yoshiki [4 ]
Nakashima, Hideki [1 ]
Kang, Jeong-Hun [5 ]
机构
[1] St Marianna Univ, Dept Microbiol, Sch Med, Kawasaki, Kanagawa 2168511, Japan
[2] Kyushu Univ, Fac Dent Sci, Dept Biomat, Higashi Ku, Fukuoka 8128582, Japan
[3] Kyushu Univ, Dept Adv Med Initiat, Fac Med Sci, Higashi Ku, Fukuoka 8128582, Japan
[4] Kyushu Univ, Dept Appl Chem, Fac Engn, Nishi Ku, Fukuoka 8190395, Japan
[5] Natl Cerebral & Cardiovasc Ctr, Div Biopharmaceut & Pharmacokinet, Dept Biomed Engn, Res Inst, Suita, Osaka 5658565, Japan
关键词
G protein-coupled receptor kinase; Peptide substrate; Phosphorylation; Cellular signal transduction pathway; Consensus sequence; PHOSPHORYLATION; BETA; GRK2; IDENTIFICATION; ANTAGONIST; EXPRESSION; SITES;
D O I
10.1016/j.febslet.2014.04.038
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 (GRICs) control the signaling and activation of G protein-coupled receptors through phosphorylation. In this study, consensus substrate motifs for GRK2 were identified from the sequences of GRK2 protein substrates, and 17 candidate peptides were synthesized to identify peptide substrates with high affinity for GRK2. GRK2 appears to require an acidic amino acid at the -2, -3, or -4 positions and its consensus phosphorylation site motifs were identified as (D/ E)X1-3(S/T), (D/E)X1-3(S/T)(D/E), or (D/E)X0-2(D/E)(S/T). Among the 17 peptide substrates examined, a 13-amino-acid peptide fragment of beta-tubulin (DEMEFTEAESNMN) showed the highest affinity for GRK2 (K-m, 33.9 mu M; V-max, 0.35 pmol min(-1) mg(-1)), but very low affinity for GRIC5. This peptide may be a useful tool for investigating cellular signaling pathways regulated by GRK2. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2129 / 2132
页数:4
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