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Author Notes:

Correspondence should be addressed to: Victor Faundez vfaunde@emory.edu

Subjects:

Research Funding:

This work was supported by grants from the National Institutes of Health (GM077569 and NS42599) and CHOA Children’s Center for Neuroscience to V.F. P.V.R. was supported by National Research Service Award Fellowship F31NS0765.

Keywords:

  • Cross-linking
  • Endosome
  • Interactome
  • Mass spectrometry
  • Phosphatidylinositol
  • Phosphatidylinositol kinase
  • Phosphoinositide
  • Phospholipid
  • Animals
  • Carrier Proteins
  • Chromatography, Affinity
  • Humans
  • Immunoprecipitation
  • Minor Histocompatibility Antigens
  • Phosphotransferases (Alcohol Group Acceptor)
  • Protein Binding
  • Protein Interaction Mapping

Identification of the interactome of a palmitoylated membrane protein, phosphatidylinositol 4-Kinase type II Alpha

Tools:

Journal Title:

Methods in Molecular Biology

Volume:

Volume 1376

Publisher:

, Pages 35-42

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Phosphatidylinositol 4-kinases (PI4K) are enzymes responsible for the production of phosphatidylinositol 4-phosphates, important intermediates in several cell signaling pathways. PI4KIIα is the most abundant membrane-associated kinase in mammalian cells and is involved in a variety of essential cellular functions. However, the precise role(s) of PI4KIIα in the cell is not yet completely deciphered. Here we present an experimental protocol that uses a chemical cross-linker, DSP, combined with immunoprecipitation and immunoaffinity purification to identify novel PI4KIIα interactors. As predicted, PI4KIIα participates in transient, low-affinity interactions that are stabilized by the use of DSP. Using this optimized protocol we have successfully identified actin cytoskeleton regulators—the WASH complex and RhoGEF1, as major novel interactors of PI4KIIα. While this chapter focuses on the PI4KIIα interactome, this protocol can and has been used to generate other membrane interactome networks.

Copyright information:

© Springer Science+Business Media New York 2016.

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