Journal of Chemical Information and ModelingBioinformaticsPeer-reviewed journal article
Water will find its way: transport through narrow tunnels in hydrolases
Carlos Eduardo Sequeiros-BorjaiD, Bartłomiej SurpetaiD, Aravind Selvaram ThirunavukarasuiD, Cedrix J. Dongmo FoumthuimiD, Igor MarchlewskiiD, Jan BrezovskýiD
Abstract
An aqueous environment is vital for life as we know it, and water is essential for nearly all biochemical processes at a molecular level. Proteins utilize water molecules in various ways. Consequently, proteins must transport water molecules across their internal network of tunnels to reach the desired action sites, either within them or functioning as molecular pipes to control cellular osmotic pressure. Despite water playing a crucial role in enzymatic activity and stability, its transport has been largely overlooked, with studies primarily focusing on water transport across membrane proteins. The transport of molecules through a proteins tunnel network is challenging to study experimentally, making molecular dynamics simulations the most popular approach for investigating such events. In this study, we focused on the transport of water molecules across three different /{beta}-hydrolases: haloalkane dehalogenase, epoxide hydrolase, and lipase. Using a 5 s adaptive simulation per system, we observed that only a few tunnels were responsible for the majority of water transport in dehalogenase, in contrast to a higher diversity of tunnels in other enzymes. Interestingly, water molecules could traverse narrow tunnels with sub-angstrom bottlenecks, which is surprising given the commonly accepted water molecule radius of 1.4 [A]. Our analysis of the transport events in such narrow tunnels revealed a markedly increased number of hydrogen bonds formed between the water molecules and the protein, likely compensating for the steric penalty of the process. Overall, these commonly disregarded narrow tunnels accounted for [~]20% of the total water transport observed, emphasizing the need to surpass the standard geometrical limits on the functional tunnels to properly account for relevant transport processes. Finally, we demonstrated how the obtained insights could be applied to explain the differences in a mutant of the human soluble epoxide hydrolase associated with a higher incidence of ischemic stroke.
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