Spontaneous Reactivation of OPC-Inhibited BChE Mutants: Modeling of Mechanisms

The mechanism of the reactivation reaction of the double mutant butyrylcholinesterase (BChE) double mutantAsn322Glu/Glu325Gly, inhibited by the organophosphorus compound (OPC) echothiophat is studied by molecular modeling methods. The ability of this mutant to spontaneously reactivate itself was pre...

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Veröffentlicht in:Russian journal of physical chemistry. B 2022-02, Vol.16 (1), p.103-108
Hauptverfasser: Lushchekina, S. V., Nemukhin, A. V., Polyakov, I. V., Masson, P., Varfolomeev, S. D., Grigorenko, B. L.
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Sprache:eng
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Zusammenfassung:The mechanism of the reactivation reaction of the double mutant butyrylcholinesterase (BChE) double mutantAsn322Glu/Glu325Gly, inhibited by the organophosphorus compound (OPC) echothiophat is studied by molecular modeling methods. The ability of this mutant to spontaneously reactivate itself was previously shown experimentally. The energy profile of the reaction path calculated by the method of quantum mechanics/molecular mechanics (QM/MM) confirms that such a mechanism is possible. Molecular dynamics calculations with QM/MM potentials are used to investigate the proton transfer pathways and determine the protonated state of the glutamic acids in the active site of the double mutant. Possible ways of increasing its conformational stability are investigated by the methods of classical molecular dynamics.
ISSN:1990-7931
1990-7923
DOI:10.1134/S1990793122010237