Autoantigen Ro52 directly interacts with human IgG heavy chain in vivo in mammalian cells

Yih Sheng Yang, Bin Wang, Jonathan C. Weissler

Research output: Contribution to journalArticle

19 Scopus citations

Abstract

Previously, when we used in vivo yeast two-hybrid and in vitro protein-protein interaction analyses, we demonstrated a direct interaction between autoantigen Ro52 and the human IgG heavy chain. This interaction occurred in the absence of antibody-antigen specific interaction. Here, by employing a novel strategy, we further demonstrated that Ro52 co-localized with IgG in transfected mammalian cells. The co-localization was specific to IgG1 but not IgG3. Co-immunoprecipitating IgG with Ro52 from transfected cell lysates suggested that protein complex containing Ro52 and IgG contributed to the in vivo co-localization. In addition, IgG from normal human serum was shown to bind to the surface of apoptotic keratinocytes and the binding could be competitively blocked by 50-fold excesses of IgG1, not IgG3. With a direct binding study, we also demonstrated that IgG1 could bind to the surface of apoptotic cells while IgG3 bound barely. This binding was not competed by Fcγ fragments indicating a non-Fcγ receptor mediated interaction. Finally, in a competition analysis the addition of GST-RFP could reduce the IgG binding to the cell surface. Thus, we suggested that the binding of IgG to the apoptotic keratinocytes might be mediated through the interactions with the surface exposed Ro52. The potential role of forming this protein complex on the apoptotic cells will be discussed.

Original languageEnglish (US)
Pages (from-to)591-602
Number of pages12
JournalMolecular Immunology
Volume37
Issue number10
DOIs
StatePublished - 2000

Keywords

  • Apoptosis
  • Autoantigen
  • Estrogen receptor
  • IgG
  • Mammalian two-hybrid analysis
  • Ro52

ASJC Scopus subject areas

  • Immunology
  • Molecular Biology

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