Mutation D816V Alters the Internal Structure and Dynamics of c-KIT Receptor Cytoplasmic Region: Implications for Dimerization and Activation Mechanisms

• DOI: 10.1371/journal.pcbi.1002068
• Publication Date: 2011-11-26T22:51:32Z
• Authors: Elodie Laine; Isaure Chauvot de...; David Perahia; Christian Auclair; Luba Tchertanov
• Keywords: QH301-705.5; Antineoplastic Agents; Molecular Dynamics Simulation; tyrosine-kinase; Piperazines; 03 medical and health sciences; Catalytic Domain; Humans; Biology (General); Principal Component Analysis; 0303 health sciences; Protein Stability; KIT; [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology; 3. Good health; Proto-Oncogene Proteins c-kit; D816V; molecular dynamics simulation; Pyrimidines; Drug Resistance, Neoplasm; Benzamides; Mutation; Imatinib Mesylate; Thermodynamics; [INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM]; Dimerization; Research Article

The type III receptor tyrosine kinase (RTK) KIT plays a crucial role in the transmission of cellular signals through phosphorylation events that are associated with a switching of the protein conformation between inactive and active states. D816V KIT mutation is associated with various pathologies including mastocytosis and cancers. D816V-mutated KIT is constitutively active, and resistant to treatment with the anti-cancer drug Imatinib. To elucidate the activating molecular mechanism of this mutation, we applied a multi-approach procedure combining molecular dynamics (MD) simulations, normal modes analysis (NMA) and binding site prediction. Multiple 50-ns MD simulations of wild-type KIT and its mutant D816V were recorded using the inactive auto-inhibited structure of the protein, characteristic of type III RTKs. Computed free energy differences enabled us to quantify the impact of D816V on protein stability in the inactive state. We evidenced a local structural alteration of the activation loop (A-loop) upon mutation, and a long-range structural re-organization of the juxta-membrane region (JMR) followed by a weakening of the interaction network with the kinase domain. A thorough normal mode analysis of several MD conformations led to a plausible molecular rationale to propose that JMR is able to depart its auto-inhibitory position more easily in the mutant than in wild-type KIT and is thus able to promote kinase mutant dimerization without the need for extra-cellular ligand binding. Pocket detection at the surface of NMA-displaced conformations finally revealed that detachment of JMR from the kinase domain in the mutant was sufficient to open an access to the catalytic and substrate binding sites.