Role of phosphatidylinositol 3,4,5-trisphosphate in regulating the activity and localization of 3-phosphoinositide-dependent protein kinase-1

Richard A. Currie (Lead / Corresponding author), Kay S. Walker, Alex Gray, Maria Deak, Antonio Casamayor, C. Peter Downes, Philip Cohen, Dario R. Alessi, John Lucocq

Research output: Contribution to journalArticlepeer-review

295 Citations (Scopus)

Abstract

3-Phosphoinositide-dependent protein kinase-1 (PDK1) interacts stereoselectively with the D-enantiomer of PtdIns(3,4,5)P3 (KD 1.6 nM) and PtdIns(3,4)P2 (KD 5.2 nM), but binds with lower affinity to PtdIns3P or PtdIns(4,5)P2. The binding of Ptd-Ins(3,4,5)P3 to PDK1 was greatly decreased by making specific mutations in the pleckstrin homology (PH) domain of PDK1 or by deleting it. The same mutations also greatly decreased the rate at which PDK1 activated protein kinase Bα (PKBα) in vitro in the presence of lipid vesicles containing PtdIns(3,4,5)P3, but did not affect the rate at which PDK1 activated a PKBα mutant lacking the PH domain in the absence of PtdIns(3,4,5)P3. When overexpressed in 293 or PAE cells, PDK1 was located at the plasma membrane and in the cytosol, but was excluded from the nucleus. Mutations that disrupted the interaction of Ptd-Ins(3,4,5)P3 or PtdIns(4,5)P2 with PDK1 abolished the association of PDK1 with the plasma membrane. Growth-factor stimulation promoted the translocation of transfected PKBα to the plasma membrane, but had no effect on the subcellular distribution of PDK1 as judged by immunoelectron microscopy of fixed cells. This conclusion was also supported by confocal microscopy of green fluorescent protein-PDK1 in live cells. These results, together with previous observations, indicate that PtdIns(3,4,5)P3 plays several roles in the PDK1-induced activation of PKBα. First, it binds to the PH domain of PKB, altering its conformation so that it can be activated by PDK1. Secondly, interaction with PtdIns(3,4,5),P3 recruits PKB to the plasma membrane with which PDK1 is localized constitutively by virtue of its much stronger interaction with PtdIns(3,4,5)P3 or PtdIns(4,5)P2. Thirdly, the interaction of PDK1 with PtdIns (3,4,5)P3 facilitates the rate at which it can activate PKB.

Original languageEnglish
Pages (from-to)575-583
Number of pages9
JournalBiochemical Journal
Volume337
Issue number2-3
DOIs
Publication statusPublished - 1 Feb 1999

Keywords

  • Lipid binding
  • Protein kinase B
  • Signal transduction
  • Surface plasmon resonance

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