Phosphorylation of the stress-activated protein kinase, MEKK3, at serine 166

Deanna G. Adams, Nancy A. Sachs, Richard R. Vaillancourt

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Much effort has focused on the identification of MAPK cascades that are activated by the MEKK family of protein kinases. However, direct phosphorylation and regulation of the MEKK proteins has not been shown. To address this question, we have expressed recombinant (His)6FLAG·MEKK3 in Sf9 insect cells and tethered the purified protein to Ni-Sepharose so that we could precipitate interacting proteins and then identify such proteins by liquid chromatography and mass spectrometry (LC-MS). We identified 14-3-3 proteins as interacting with MEKK3, which suggested that (His)6FLAG·MEKK3 was phosphorylated on serine since 14-3-3 proteins are known to associate with phosphorylated proteins. We identified two phosphorylated amino acids at Ser166 and Ser337 of tryptic peptides derived from (His)6FLAG·MEKK3 by using LC-MS. Antibodies were developed that recognize the specific phosphorylated amino acid and with these antibodies, we demonstrate that various stimuli (tumor necrosis factor, arsenite, forskolin, and serum) promote phosphorylation of Ser166 and Ser337. However, neither of these phosphorylated amino acids is required for association with 14-3-3 protein or regulation of MEKK3-dependent ERK and JNK activity. Nonetheless, these results suggest that MEKK3 is a convergence point of multiple upstream signaling pathways.

Original languageEnglish (US)
Pages (from-to)103-116
Number of pages14
JournalArchives of Biochemistry and Biophysics
Volume407
Issue number1
DOIs
StatePublished - 2002

Keywords

  • 14-3-3
  • Liquid chromatography and tandem mass spectrometry (LC-MS)
  • MAP kinase
  • MEKK3
  • Sf9 insect cells

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology

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