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bioRxiv · 10.1101/198341

Allosteric Modulation of Conformational Dynamics in Human Hsp90?: A Computational Study

Penkler, D. L.·Atilgan, C.·Tastan Bishop, O.
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Abstract

Central to Hsp90s biological function is its ability to interconvert between various conformational states. Drug targeting of Hsp90s regulatory mechanisms, including its modulation by co-chaperone association, presents as an attractive therapeutic strategy for Hsp90 associated pathologies. Here, we utilize homology modeling techniques to calculate full-length structures of human Hsp90 in closed and partially-open conformations. Atomistic simulations of these structures demonstrated that bound ATP stabilizes the dimer by tensing each protomer, while ADP and apo configurations relax the complex by increasing global flexibility. Dynamic residue network analysis revealed regions of the protein involved in intra-protein communication, and identified several overlapping key communication hubs that correlate with known functional sites. Perturbation response scanning analysis identified several potential residue sites capable of modulating conformational change in favour of interstate conversion. For the ATP-bound open conformation, these sites were found to overlap with known Aha1 and client binding sites, demonstrating how naturally occurring forces associated with co-factor binding could allosterically modulate conformational dynamics.

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Penkler, D. L., Atilgan, C., Tastan Bishop, O.. 2017-10-04. Allosteric Modulation of Conformational Dynamics in Human Hsp90?: A Computational Study. https://doi.org/10.1101/198341

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