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梭曼抑制的胆碱酯酶及其突变体中脱烷基作用的pH依赖性:推拉机制的进一步证据。

The pH dependence of dealkylation in soman-inhibited cholinesterases and their mutants: further evidence for a push-pull mechanism.

作者信息

Saxena A, Viragh C, Frazier D S, Kovach I M, Maxwell D M, Lockridge O, Doctor B P

机构信息

Division of Biochemistry, Walter Reed Army Institute of Research, Washington, D.C. 20307, USA.

出版信息

Biochemistry. 1998 Oct 27;37(43):15086-96. doi: 10.1021/bi980917z.

Abstract

Bimolecular rate constants for the inactivation of recombinant (r) human (Hu) butyrylcholinesterase (BChE) with P(S)C(S)- and P(S)C(R)-2-(3,3-dimethylbutyl) methylphosphonofluoridate (soman) are (92 +/- 7) x 10(6) M-1 min-1 and (13.7 +/- 0.8) x 10(6) M-1 min-1 at pH 7.4, mu = 0.1 M and 25 degreesC. Mutations of E197(199) to D or Q and W82(84) to A result in reductions in the rate constants for inactivation with P(S)C(S)-soman 4.3-, 11.8-, and 263-fold and with P(S)C(R)-soman by 6.5-, 47.3-, and 685-fold, respectively. The pH dependence of dealkylation (aging) in r mouse (Mo) acetylcholinesterase (AChE) and rHu BChE and their mutants inactivated with P(S)C(S)- and P(S)C(R)-soman was compared. Best-fit parameters for the asymmetric bell curves for the adducts of wild-type Mo AChE are pK1 = pK2 = 4.0-4.9 and pK3 = 5.2-6.6. These pKs are consistent with the involvement of two carboxylic acids, possibly E202(199) and either E334(327) or E450(443), and H447(440)H+ in the dealkylation of AChE. E202Q MoAChE inactivated with the soman diastereomers yielded pK3 = 5.5-5.8. Nearly symmetric pH curves for soman-inhibited wild-type and E197D Hu BChE gave pK2 = 3.7-4.6 and pK3 = 7.3-8.0, but much lower, pK3 approximately 5, for the corresponding adduct of the E197Q mutant. Dealkylation in soman-inhibited BChE is consistent with the participation of one carboxylic acid side chain and H438(440)H+. Maximal rate constants for dealkylation (kmax) are 1-6 min-1 for AChE and 2 min-1 for BChE at 25 degreesC. The W82 to A mutation in BChE results in the largest reduction, 2500-6000-fold, in the rate constant for dealkylation. The reduction in the rate constants for dealkylation in the E197 mutants is highly pH dependent. The solvent isotope effects at the pH maxima are 1.3-1.4, indicating unlikely preprotonation or proton in "flight" at the enzymic transition states. The new results support the push-pull mechanism of dealkylation in soman-inhibited cholinesterases proposed previously.

摘要

在pH 7.4、离子强度μ = 0.1 M及25℃条件下,重组(r)人(Hu)丁酰胆碱酯酶(BChE)与P(S)C(S)-和P(S)C(R)-2-(3,3-二甲基丁基)甲基膦酰氟(梭曼)失活反应的双分子速率常数分别为(92 ± 7)×10⁶ M⁻¹ min⁻¹和(13.7 ± 0.8)×10⁶ M⁻¹ min⁻¹。E197(199)突变为D或Q以及W82(84)突变为A,会使P(S)C(S)-梭曼失活反应的速率常数分别降低4.3倍、11.8倍和263倍,使P(S)C(R)-梭曼失活反应的速率常数分别降低6.5倍、47.3倍和685倍。比较了r小鼠(Mo)乙酰胆碱酯酶(AChE)和rHu BChE及其用P(S)C(S)-和P(S)C(R)-梭曼失活的突变体中脱烷基化(老化)的pH依赖性。野生型Mo AChE加合物的不对称钟形曲线的最佳拟合参数为pK1 = pK2 = 4.0 - 4.9,pK3 = 5.2 - 6.6。这些pK值与两种羧酸(可能是E202(199)和E334(327)或E450(443))以及H447(440)H⁺参与AChE脱烷基化反应一致。用梭曼非对映体失活的E202Q MoAChE得到pK3 = 5.5 - 5.8。梭曼抑制的野生型和E197D Hu BChE的几乎对称的pH曲线给出pK2 = 3.7 - 4.6,pK3 = 7.3 - 8.0,但E197Q突变体的相应加合物的pK3约为5,低得多。梭曼抑制的BChE中的脱烷基化与一个羧酸侧链和H438(440)H⁺的参与一致。在25℃时,AChE脱烷基化的最大速率常数(kmax)为1 - 6 min⁻¹,BChE为2 min⁻¹。BChE中W82突变为A导致脱烷基化速率常数最大降低2500 - 6000倍。E197突变体中脱烷基化速率常数的降低高度依赖于pH。在pH最大值处的溶剂同位素效应为1.3 - 1.4,表明在酶促过渡态不太可能存在预质子化或“飞行”中的质子。新结果支持先前提出的梭曼抑制的胆碱酯酶中脱烷基化的推拉机制。

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