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3'-脱氧-3',4'-二脱氢胞苷三磷酸(ddhCTP)的化学酶法合成

Chemoenzymatic Synthesis of 3'-Deoxy-3',4'-didehydro-cytidine triphosphate (ddhCTP).

作者信息

Lee James H, Wood James M, Almo Steven C, Evans Gary B, Harris Lawrence D, Grove Tyler L

机构信息

Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461, United States.

Ferrier Research Institute, Victoria University of Wellington, Wellington 6012, New Zealand.

出版信息

ACS Bio Med Chem Au. 2023 Jul 25;3(4):322-326. doi: 10.1021/acsbiomedchemau.3c00014. eCollection 2023 Aug 16.

Abstract

3'-Deoxy-3',4'-didehydro-cytidine triphosphate (ddhCTP) is a novel antiviral molecule produced by the enzyme viperin during the early stages of the innate immune response. ddhCTP has been shown to act as a chain terminator of flavivirus RNA-dependent RNA polymerases. To date, synthesis of ddhCTP requires complicated synthetic protocols or isolation of the enzyme viperin to catalyze the production of ddhCTP from CTP. Recombinant viperin approaches preclude the production of highly pure ddhCTP (free of contaminants such as CTP), whereas the chemical synthesis involves techniques or equipment not readily available to most laboratories. Herein, we describe the chemoenzymatic synthesis of ddhCTP, starting from commercially available ddhC. We utilize these methods to produce milligram quantities of ddhCTP, ddhCDP, and ddhCMP. Using purified semisynthetic ddhCTP and fully synthetic ddhCTP, we also show ddhCTP does not inhibit NAD-dependent enzymes such as glyceraldehyde 3-phosphate dehydrogenase, malate dehydrogenase, or lactate dehydrogenase, contrary to a recent report.

摘要

3'-脱氧-3',4'-二脱氢胞苷三磷酸(ddhCTP)是一种新型抗病毒分子,由蝰蛇毒蛋白在先天免疫反应早期产生。已证明ddhCTP可作为黄病毒RNA依赖性RNA聚合酶的链终止剂。迄今为止,ddhCTP的合成需要复杂的合成方案或分离蝰蛇毒蛋白以催化从CTP生成ddhCTP。重组蝰蛇毒蛋白方法无法生产高纯度的ddhCTP(不含CTP等污染物),而化学合成涉及大多数实验室不易获得的技术或设备。在此,我们描述了从市售的ddhC开始的ddhCTP的化学酶促合成。我们利用这些方法生产毫克量的ddhCTP、ddhCDP和ddhCMP。使用纯化的半合成ddhCTP和全合成ddhCTP,我们还表明,与最近的一份报告相反,ddhCTP不会抑制NAD依赖性酶,如甘油醛-3-磷酸脱氢酶、苹果酸脱氢酶或乳酸脱氢酶。

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