Peptide substrates for G protein-coupled receptor kinase 2

Daisuke Asai, Riki Toita, Masaharu Murata, Yoshiki Katayama, Hideki Nakashima, Jeong Hun Kang

    Research output: Contribution to journalArticlepeer-review

    11 Citations (Scopus)

    Abstract

    G protein-coupled receptor kinases (GRKs) 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 β-tubulin (DEMEFTEAESNMN) showed the highest affinity for GRK2 (Km, 33.9 μM; Vmax, 0.35 pmol min-1 mg-1), but very low affinity for GRK5. This peptide may be a useful tool for investigating cellular signaling pathways regulated by GRK2.

    Original languageEnglish
    Pages (from-to)2129-2132
    Number of pages4
    JournalFEBS Letters
    Volume588
    Issue number13
    DOIs
    Publication statusPublished - Jun 13 2014

    All Science Journal Classification (ASJC) codes

    • Biophysics
    • Structural Biology
    • Biochemistry
    • Molecular Biology
    • Genetics
    • Cell Biology

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