Global phosphorylation analysis of β-arrestin-mediated signaling downstream of a seven transmembrane receptor (7TMR)

Kunhong Xiao, Jinpeng Sun, Jihee Kim, Sudarshan Rajagopal, Bo Zhai, Judit Villén, Wilhelm Haas, Jeffrey J. Kovacs, Arun K. Shukla, Makoto R. Hara, Marylens Hernandez, Alexander Lachmann, Shan Zhao, Yuan Lin, Yishan Cheng, Kensaku Mizuno, Avi Ma'ayan, Steven P. Gygi, Robert J. Lefkowitz

    Research output: Contribution to journalArticlepeer-review

    148 Citations (Scopus)

    Abstract

    β-Arrestin-mediated signaling downstream of seven transmembrane receptors (7TMRs) is a relatively new paradigm for signaling by these receptors. We examined changes in protein phosphorylation occurring when HEK293 cells expressing the angiotensin II type 1A receptor (AT1aR) were stimulated with the β-arrestin-biased ligand Sar1, Ile4, Ile 8-angiotensin (SII), a ligand previously found to signal through β-arrestin-dependent, G protein-independent mechanisms. Using a phospho-antibody array containing 46 antibodies against signaling molecules, we found that phosphorylation of 35 proteins increased upon SII stimulation. These SII-mediated phosphorylation events were abrogated after depletion of β-arrestin 2 through siRNA-mediated knockdown. We also performed an MS-based quantitative phosphoproteome analysis after SII stimulation using a strategy of stable isotope labeling of amino acids in cell culture (SILAC).We identified 1,555 phosphoproteins (4,552 unique phosphopeptides), of which 171 proteins (222 phosphopeptides) showed increased phosphorylation, and 53 (66 phosphopeptides) showed decreased phosphorylation upon SII stimulation of the AT1aR. This study identified 38 protein kinases and three phosphatases whose phosphorylation status changed upon SII treatment. Using computational approaches, we performed system-based analyses examining the β-arrestin-mediated phosphoproteome including construction of a kinase-substrate network for β-arrestin-mediated AT1aR signaling. Our analysis demonstrates that β-arrestin-dependent signaling processes are more diverse than previously appreciated. Notably, our analysis identifies an AT1aR-mediated cytoskeletal reorganization network whereby β-arrestin regulates phosphorylation of several key proteins, including cofilin and slingshot. This study provides a system-based view of β-arrestin-mediated phosphorylation events downstream of a 7TMR and opens avenues for research in a rapidly evolving area of 7TMR signaling.

    Original languageEnglish
    Pages (from-to)15299-15304
    Number of pages6
    JournalProceedings of the National Academy of Sciences of the United States of America
    Volume107
    Issue number34
    DOIs
    Publication statusPublished - 2010 Aug 24

    Keywords

    • G protein-coupled receptor
    • GPCR
    • Phosphoproteome

    ASJC Scopus subject areas

    • General

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