An in silico study of the molecular basis of B-RAF activation and conformational stability

Abstract

Background. B-RAF kinase plays an important role both in tumour induction and maintenance in several cancers and it is an attractive new drug target. However, the structural basis of the B-RAF activation is still not well understood. Results. In this study we suggest a novel molecular basis of B-RAF activation based on molecular dynamics (MD) simulations of B-RAFWTand the B-RAFV600E, B-RAFK601Eand B-RAF D594Vmutants. A strong hydrogen bond network was identified in B-RAFWTin which the interactions between Lys601 and the well known catalytic residues Lys483, Glu501 and Asp594 play an important role. It was found that several mutations, which directly or indirectly destabilized the interactions between these residues within this network, contributed to the changes in B-RAF activity. Conclusion. Our results showed that the above mechanisms lead to the disruption of the electrostatic interactions between the A-loop and the C-helix in the activating mutants, which presumably contribute to the flipping of the activation segment to an active form. Conversely, in the B-RAFD594Vmutant that has impaired kinase activity, and in B-RAF WTthese interactions were strong and stabilized the kinase inactive form. © 2009 Fratev and Jnsdttir; licensee BioMed Central Ltd.