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Crystal structures of acetylcholinesterase in complex with organophosphorus compounds suggest that the acyl pocket modulates the aging reaction by precluding the formation of the trigonal bipyramidal transition state.乙酰胆碱酯酶与有机磷化合物复合物的晶体结构表明,酰基口袋通过阻止三角双锥过渡态的形成来调节老化反应。
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Probing the acetylcholinesterase inhibition of sarin: a comparative interaction study of the inhibitor and acetylcholine with a model enzyme cavity.探究沙林对乙酰胆碱酯酶的抑制作用:抑制剂与乙酰胆碱在模型酶腔中的相互作用比较研究
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Ab initio molecular orbital and density functional studies on the solvolysis of sarin and O,S-dimethyl methylphosphonothiolate, a VX-like compound.关于沙林和一种类VX化合物O,S-二甲基甲基硫代磷酸酯溶剂解的从头算分子轨道和密度泛函研究。
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沙林与乙酰胆碱酯酶相互作用的反应轮廓和 S203C 突变体:模型亲核试剂和 QM/MM 势能面。

Reaction profiles of the interaction between sarin and acetylcholinesterase and the S203C mutant: model nucleophiles and QM/MM potential energy surfaces.

机构信息

Department of Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus, OH 43210, USA.

出版信息

Chem Biol Interact. 2010 Sep 6;187(1-3):220-4. doi: 10.1016/j.cbi.2010.02.012. Epub 2010 Feb 13.

DOI:10.1016/j.cbi.2010.02.012
PMID:20156428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2894988/
Abstract

The phosphonylation mechanism of AChE and the S203C mutation by sarin (GB) is evaluated using two reaction schemes: a small model nucleophile (ethoxide, CH(3)CH(2)O(-)) and quantum mechanical/molecular mechanical (QM/MM) simulations. Calculations utilizing small model nucleophiles indicate that the reaction barrier for addition to GB is the rate-limiting step for both ethoxide and ethyl thiolate (CH(3)CH(2)S(-)); moreover, the activation barrier for addition to the phosphorus center of GB by ethyl thiolate is significantly larger (13.2 kcal/mol) than for ethoxide (8.3 kcal/mol). The decomposition transition state for both nucleophiles was determined to be approximately 1 kcal/mol. QM/MM simulations for AChE suggest a similar reaction mechanism for phosphonylation of the catalytic S203; however, the relative energetics are altered significantly compared to the isolated system. QM/MM results indicate that formation of the penta-coordinate intermediate is the rate-limiting step in the enzymatic system, with an activation barrier of 3.6 kcal/mol. Hydrogen-bonding interactions between the fluoride leaving group of GB with Y124 in AChE are observed throughout the reaction profile. The S203C mutation alters the relative energetics of the reaction, increasing the energy barrier for formation of the penta-coordinate intermediate to a value of 4.5 kcal/mol; moreover, the penta-coordinate intermediate (as product) is stabilized by an additional 6 kcal/mol when compared to wild-type AChE.

摘要

使用两种反应方案评估了 AChE 的膦酰化机制和沙林(GB)的 S203C 突变:一个小的模型亲核试剂(乙氧基,CH(3)CH(2)O(-))和量子力学/分子力学(QM/MM)模拟。利用小模型亲核试剂的计算表明,对于 GB 的加成反应,对于乙氧基和乙基硫醇盐(CH(3)CH(2)S(-))来说都是限速步骤;此外,乙基硫醇盐加到 GB 的磷中心的活化能垒明显更大(13.2 kcal/mol)比乙氧基(8.3 kcal/mol)。对于两种亲核试剂,分解过渡态被确定为大约 1 kcal/mol。对于 AChE 的 QM/MM 模拟表明,对于催化 S203 的膦酰化,存在类似的反应机制;然而,与孤立体系相比,相对能量发生了很大的变化。QM/MM 结果表明,五配位中间体的形成是酶系统中磷酰化的限速步骤,其活化能垒为 3.6 kcal/mol。在整个反应过程中,观察到 GB 的离去氟与 AChE 中的 Y124 之间的氢键相互作用。S203C 突变改变了反应的相对能量,使五配位中间体的形成能垒增加到 4.5 kcal/mol;此外,与野生型 AChE 相比,五配位中间体(作为产物)的稳定性增加了 6 kcal/mol。