Water regulates the residence time of Benzamidine in Trypsin

Narjes Ansari, Valerio Rizzi and Michele Parrinello ()
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Narjes Ansari: Italian Institute of Technology
Valerio Rizzi: Italian Institute of Technology
Michele Parrinello: Italian Institute of Technology

Nature Communications, 2022, vol. 13, issue 1, 1-9

Abstract: Abstract The process of ligand-protein unbinding is crucial in biophysics. Water is an essential part of any biological system and yet, many aspects of its role remain elusive. Here, we simulate with state-of-the-art enhanced sampling techniques the binding of Benzamidine to Trypsin which is a much studied and paradigmatic ligand-protein system. We use machine learning methods to determine efficient collective coordinates for the complex non-local network of water. These coordinates are used to perform On-the-fly Probability Enhanced Sampling simulations, which we adapt to calculate also the ligand residence time. Our results, both static and dynamic, are in good agreement with experiments. We find that the presence of a water molecule located at the bottom of the binding pocket allows via a network of hydrogen bonds the ligand to be released into the solution. On a finer scale, even when unbinding is allowed, another water molecule further modulates the exit time.

Date: 2022
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DOI: 10.1038/s41467-022-33104-3

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