DFG-flip" in the insulin receptor kinase is facilitated by a helical intermediate state of the activation loop.

Harish Vashisth, Luca Maragliano, Cameron F Abrams

Biophysical journal 2012 Apr 18

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We have characterized a large-scale inactive-to-active conformational change in the activation-loop of the insulin receptor kinase domain at the atomistic level via untargeted temperature-accelerated molecular dynamics (TAMD) and free-energy calculations using the string method. TAMD simulations consistently show folding of the A-loop into a helical conformation followed by unfolding to an active conformation, causing the highly conserved DFG-motif (Asp(1150), Phe(1151), and Gly(1152)) to switch from the inactive "D-out/F-in" to the nucleotide-binding-competent "D-in/F-out" conformation. The minimum free-energy path computed from the string method preserves these helical intermediates along the inactive-to-active path, and the thermodynamic free-energy differences are consistent with previous work on various other kinases. The mechanisms revealed by TAMD also suggest that the regulatory spine can be dynamically assembled/disassembled either by DFG-flip or by movement of the αC-helix. Together, these findings both broaden our understanding of kinase activation and point to intermediates as specific therapeutic targets. Copyright © 2012 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Citation

Harish Vashisth, Luca Maragliano, Cameron F Abrams. DFG-flip" in the insulin receptor kinase is facilitated by a helical intermediate state of the activation loop. Biophysical journal. 2012 Apr 18;102(8):1979-87