Activation pathway of Src kinase reveals intermediate states as targets for drug design

Diwakar Shukla, Yilin Meng, Benoît Roux and Vijay S. Pande ()
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Diwakar Shukla: Stanford University
Yilin Meng: Gordon Center for Integrative Science, The University of Chicago
Benoît Roux: Gordon Center for Integrative Science, The University of Chicago
Vijay S. Pande: Stanford University

Nature Communications, 2014, vol. 5, issue 1, 1-11

Abstract: Abstract Unregulated activation of Src kinases leads to aberrant signalling, uncontrolled growth and differentiation of cancerous cells. Reaching a complete mechanistic understanding of large-scale conformational transformations underlying the activation of kinases could greatly help in the development of therapeutic drugs for the treatment of these pathologies. In principle, the nature of conformational transition could be modelled in silico via atomistic molecular dynamics simulations, although this is very challenging because of the long activation timescales. Here we employ a computational paradigm that couples transition pathway techniques and Markov state model-based massively distributed simulations for mapping the conformational landscape of c-src tyrosine kinase. The computations provide the thermodynamics and kinetics of kinase activation for the first time, and help identify key structural intermediates. Furthermore, the presence of a novel allosteric site in an intermediate state of c-src that could be potentially used for drug design is predicted.

Date: 2014
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4397

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DOI: 10.1038/ncomms4397

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