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可卡因水解酶对毒性最强的可卡因代谢物去甲可卡因的催化活性。

Catalytic activities of cocaine hydrolases against the most toxic cocaine metabolite norcocaethylene.

机构信息

Molecular Modeling and Biopharmaceutical Center and Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 789 South Limestone Street, Lexington, KY 40536, USA.

出版信息

Org Biomol Chem. 2020 Mar 11;18(10):1968-1977. doi: 10.1039/c9ob02762a.

DOI:10.1039/c9ob02762a
PMID:32101217
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7362898/
Abstract

A majority of cocaine users also consume alcohol. The concurrent use of cocaine and alcohol produces the pharmacologically active metabolites cocaethylene and norcocaethylene, in addition to norcocaine. Both cocaethylene and norcocaethylene are more toxic than cocaine itself. Hence, a truly valuable cocaine-metabolizing enzyme for cocaine abuse/overdose treatment should be effective for the hydrolysis of not only cocaine, but also its metabolites norcocaine, cocaethylene, and norcocaethylene. However, there has been no report on enzymes capable of hydrolyzing norcocaethylene (the most toxic metabolite of cocaine). The catalytic efficiency parameters (kcat and KM) of human butyrylcholinesterase (BChE) and two mutants (known as cocaine hydrolases E14-3 and E12-7) against norcocaethylene have been characterized in the present study for the first time, and they are compared with those against cocaine. According to the obtained kinetic data, wild-type human BChE showed a similar catalytic efficiency against norcocaethylene (kcat = 9.5 min-1, KM = 11.7 μM, and kcat/KM = 8.12 × 105 M-1 min-1) to that against (-)-cocaine (kcat = 4.1 min-1, KM = 4.5 μM, and kcat/KM = 9.1 × 105 M-1 min-1). E14-3 and E12-7 showed an improved catalytic activity against norcocaethylene compared to wild-type BChE. E12-7 showed a 39-fold improved catalytic efficiency against norcocaethylene (kcat = 210 min-1, KM = 6.6 μM, and kcat/KM = 3.18 × 107 M-1 min-1). It has been demonstrated that E12-7 as an exogenous enzyme can efficiently metabolize norcocaethylene in rats.

摘要

大多数可卡因使用者也会饮酒。可卡因和酒精的同时使用会产生具有药理活性的代谢物可乐因和去甲可乐因,此外还有去甲可卡因。可乐因和去甲可乐因都比可卡因本身更具毒性。因此,对于可卡因滥用/过量治疗真正有价值的可卡因代谢酶应该不仅对可卡因本身,而且对其代谢物去甲可卡因、可乐因和去甲可乐因的水解都有效。然而,目前还没有关于能够水解去甲可乐因(可卡因最有毒的代谢物)的酶的报道。本研究首次对人丁酰胆碱酯酶(BChE)及其两种突变体(称为可卡因水解酶 E14-3 和 E12-7)对去甲可乐因的催化效率参数(kcat 和 KM)进行了表征,并与对可卡因的进行了比较。根据获得的动力学数据,野生型人 BChE 对去甲可乐因(kcat = 9.5 min-1,KM = 11.7 μM,kcat/KM = 8.12×105 M-1 min-1)的催化效率与(-)-可卡因(kcat = 4.1 min-1,KM = 4.5 μM,kcat/KM = 9.1×105 M-1 min-1)相似。E14-3 和 E12-7 对去甲可乐因的催化活性比野生型 BChE 有所提高。E12-7 对去甲可乐因的催化效率提高了 39 倍(kcat = 210 min-1,KM = 6.6 μM,kcat/KM = 3.18×107 M-1 min-1)。研究表明,作为外源性酶的 E12-7 可以有效地在大鼠体内代谢去甲可乐因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/98f6fe20f887/nihms-1572182-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/b1effc648faf/nihms-1572182-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/98f6fe20f887/nihms-1572182-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/b1effc648faf/nihms-1572182-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/f1148c236dd3/nihms-1572182-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/9f3fc1439e16/nihms-1572182-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/78e18c4fa30e/nihms-1572182-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/8db521971b99/nihms-1572182-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9332/7362898/98f6fe20f887/nihms-1572182-f0006.jpg

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