Investigating the Structure and Dynamics of the PIK3CA Wild-Type and H1047R Oncogenic Mutant

Paraskevi Gkeka, Thomas Evangelidis, Maria Pavlaki, Vasiliki Lazani, Savvas Christoforidis, Bogos Agianian, Zoe Cournia

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

The PIK3CA gene is one of the most frequently mutated oncogenes in human cancers. It encodes p110α, the catalytic subunit of phosphatidylinositol 3-kinase alpha (PI3Kα), which activates signaling cascades leading to cell proliferation, survival, and cell growth. The most frequent mutation in PIK3CA is H1047R, which results in enzymatic overactivation. Understanding how the H1047R mutation causes the enhanced activity of the protein in atomic detail is central to developing mutant-specific therapeutics for cancer. To this end, Surface Plasmon Resonance (SPR) experiments and Molecular Dynamics (MD) simulations were carried out for both wild-type (WT) and H1047R mutant proteins. An expanded positive charge distribution on the membrane binding regions of the mutant with respect to the WT protein is observed through MD simulations, which justifies the increased ability of the mutated protein variant to bind to membranes rich in anionic lipids in our SPR experiments. Our results further support an auto-inhibitory role of the C-terminal tail in the WT protein, which is abolished in the mutant protein due to loss of crucial intermolecular interactions. Moreover, Functional Mode Analysis reveals that the H1047R mutation alters the twisting motion of the N-lobe of the kinase domain with respect to the C-lobe and shifts the position of the conserved P-loop residues in the vicinity of the active site. These findings demonstrate the dynamical and structural differences of the two proteins in atomic detail and propose a mechanism of overactivation for the mutant protein. The results may be further utilized for the design of mutant-specific PI3Kα inhibitors that exploit the altered mutant conformation.

Original languageEnglish (US)
JournalPLoS Computational Biology
Volume10
Issue number10
DOIs
StatePublished - Oct 1 2014
Externally publishedYes

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Mutant
Proteins
Protein
Mutant Proteins
mutants
protein
Phosphatidylinositol 3-Kinase
Surface Plasmon Resonance
Molecular Dynamics Simulation
proteins
Mutation
Catalytic Domain
surface plasmon resonance
mutation
molecular dynamics
Surface Plasmon
phosphatidylinositol 3-kinase
Surface plasmon resonance
Membranes
Molecular dynamics

ASJC Scopus subject areas

  • Computational Theory and Mathematics
  • Modeling and Simulation
  • Ecology, Evolution, Behavior and Systematics
  • Genetics
  • Molecular Biology
  • Ecology
  • Cellular and Molecular Neuroscience
  • Medicine(all)

Cite this

Investigating the Structure and Dynamics of the PIK3CA Wild-Type and H1047R Oncogenic Mutant. / Gkeka, Paraskevi; Evangelidis, Thomas; Pavlaki, Maria; Lazani, Vasiliki; Christoforidis, Savvas; Agianian, Bogos; Cournia, Zoe.

In: PLoS Computational Biology, Vol. 10, No. 10, 01.10.2014.

Research output: Contribution to journalArticle

Gkeka, Paraskevi ; Evangelidis, Thomas ; Pavlaki, Maria ; Lazani, Vasiliki ; Christoforidis, Savvas ; Agianian, Bogos ; Cournia, Zoe. / Investigating the Structure and Dynamics of the PIK3CA Wild-Type and H1047R Oncogenic Mutant. In: PLoS Computational Biology. 2014 ; Vol. 10, No. 10.
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