Isolation of the mTOR complexes by affinity purification

Dos D. Sarbassov, Olga Bulgakova, Rakhmet I. Bersimbaev, Tattym Shaiken

Research output: Chapter in Book/Report/Conference proceedingChapter

9 Scopus citations

Abstract

The mammalian Target Of Rapamycin (mTOR) protein is a central component of the essential and highly conserved signaling pathway that emerged as a critical effector in regulation of cell physiology. Biochemical studies defined mTOR as the protein kinase that exists at least in two distinct complexes. The first complex has been characterized as the nutrient-sensitive mTOR complex 1 that controls cell growth and cell size by regulating protein synthesis and autophagy. The second complex of mTOR has been defined as the component of growth factor signaling that functions as a major regulatory kinase of Akt/PKB. Here, we provide the detailed methods how to purify the functional complexes of mTOR by affinity purification. In the first part, we describe the purification of the distinct mTOR complexes by immunoprecipitation. Purification of the soluble mTOR complexes is explained in the second part of this chapter.

Original languageEnglish (US)
Title of host publicationmTOR
Subtitle of host publicationMethods and Protocols
EditorsThomas Weichhart
Pages59-74
Number of pages16
DOIs
StatePublished - 2012

Publication series

NameMethods in Molecular Biology
Volume821
ISSN (Print)1064-3745

Keywords

  • Affinity purification
  • Cell lysis
  • Immunoprecipitation
  • Rapamycin
  • Raptor
  • Rictor
  • mLST8
  • mTOR
  • mTOR complex 1
  • mTOR complex 2

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics

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