Label-free proteomic identification of endogenous, insulin-stimulated interaction partners of insulin receptor substrate-1

Thangiah Geetha, Paul Langlais, Moulun Luo, Rebekka Mapes, Natalie Lefort, Shu Chuan Chen, Lawrence J. Mandarino, Zhengping Yi

Research output: Contribution to journalArticle

27 Scopus citations

Abstract

Protein-protein interactions are key to most cellular processes. Tandem mass spectrometry (MS/MS)-based proteomics combined with co-immunoprecipitation (CO-IP) has emerged as a powerful approach for studying protein complexes. However, a majority of systematic proteomics studies on protein-protein interactions involve the use of protein overexpression and/or epitope-tagged bait proteins, which might affect binding stoichiometry and lead to higher false positives. Here, we report an application of a straightforward, label-free CO-IP-MS/MS method, without the use of protein overexpression or protein tags, to the investigation of changes in the abundance of endogenous proteins associated with a bait protein, which is in this case insulin receptor substrate-1 (IRS-1), under basal and insulin stimulated conditions. IRS-1 plays a central role in the insulin signaling cascade. Defects in the protein-protein interactions involving IRS-1 may lead to the development of insulin resistance and type 2 diabetes. HPLCESI- MS/MS analyses identified eleven novel endogenous insulin-stimulated IRS-1 interaction partners in L6 myotubes reproducibly, including proteins play an important role in protein dephosphorylation [protein phosphatase 1 regulatory subunit 12A, (PPP1R12A)], muscle contraction and actin cytoskeleton rearrangement, endoplasmic reticulum stress, and protein folding, as well as protein synthesis. This novel application of label-free CO-IP-MS/MS quantification to assess endogenous interaction partners of a specific protein will prove useful for understanding how various cell stimuli regulate insulin signal transduction.

Original languageEnglish (US)
Pages (from-to)457-466
Number of pages10
JournalJournal of the American Society for Mass Spectrometry
Volume22
Issue number3
DOIs
StatePublished - Mar 2011

Keywords

  • HPLC-ESI-MS/MS
  • Insulin receptor substrate-1
  • Insulin signaling complexes
  • Label-free
  • Protein-protein interactions

ASJC Scopus subject areas

  • Structural Biology
  • Spectroscopy

Fingerprint Dive into the research topics of 'Label-free proteomic identification of endogenous, insulin-stimulated interaction partners of insulin receptor substrate-1'. Together they form a unique fingerprint.

  • Cite this