Abstract
Human butyrylcholinesterase (hBChE) is currently being developed as a detoxication enzyme for stoichiometric binding and/or catalytic hydrolysis of organophosphates. Herein, we describe the use of a molecular evolution method to develop novel hBChE variants with increased resistance to stereochemically defined nerve agent model compounds of soman, sarin, and cyclosarin. Novel hBChE variants (Y332S, D340H, and Y332S/D340H) were identified with an increased resistance to nerve agent model compounds that retained robust intrinsic catalytic efficiency. Molecular dynamics simulations of these variants revealed insights into the mechanism by which these structural changes conferred nerve agent model compound resistance.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Butyrylcholinesterase / chemistry*
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Butyrylcholinesterase / genetics
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Butyrylthiocholine / chemistry
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Chemical Warfare Agents / chemistry*
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Chemical Warfare Agents / toxicity
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Cholinesterase Inhibitors / chemistry
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Directed Molecular Evolution
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Humans
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Hydrolysis
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Kinetics
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Molecular Dynamics Simulation
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Organophosphorus Compounds / chemistry*
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Organophosphorus Compounds / toxicity
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Recombinant Proteins / chemistry
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Recombinant Proteins / genetics
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Sarin / chemistry*
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Sarin / toxicity
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Soman / chemistry*
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Soman / toxicity
Substances
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Chemical Warfare Agents
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Cholinesterase Inhibitors
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Organophosphorus Compounds
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Recombinant Proteins
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Butyrylthiocholine
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Soman
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Sarin
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Butyrylcholinesterase
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cyclohexyl methylphosphonofluoridate