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

被引:3
作者
Lee, James H. H. [1 ]
Wood, James M. M. [2 ,3 ]
Almo, Steven C. C. [1 ]
Evans, Gary B. B. [2 ,3 ]
Harris, Lawrence D. D. [2 ,3 ]
Grove, Tyler L. L. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10461 USA
[2] Victoria Univ Wellington, Ferrier Res Inst, Wellington 6012, New Zealand
[3] Univ Auckland, Maurice Wilkins Ctr Mol Biodiscovery, Auckland 1010, New Zealand
来源
ACS BIO & MED CHEM AU | 2023年 / 3卷 / 04期
关键词
Viperin; ddhCTP; GAPDH; chemoenzymaticsynthesis; anion exchange chromatography; C VIRUS-REPLICATION; VIPERIN; PROTEIN; MECHANISM;
D O I
10.1021/acsbiomedchemau.3c00014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
3 & PRIME;-Deoxy-3 & PRIME;,4 & PRIME;-didehydro-cytidinetriphosphate(ddhCTP) is a novel antiviral molecule produced by the enzyme viperinduring the early stages of the innate immune response. ddhCTP hasbeen shown to act as a chain terminator of flavivirus RNA-dependentRNA polymerases. To date, synthesis of ddhCTP requires complicatedsynthetic protocols or isolation of the enzyme viperin to catalyzethe production of ddhCTP from CTP. Recombinant viperin approachespreclude the production of highly pure ddhCTP (free of contaminantssuch as CTP), whereas the chemical synthesis involves techniques orequipment not readily available to most laboratories. Herein, we describethe chemoenzymatic synthesis of ddhCTP, starting from commerciallyavailable ddhC. We utilize these methods to produce milligram quantitiesof ddhCTP, ddhCDP, and ddhCMP. Using purified semisynthetic ddhCTPand 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 recentreport.
引用
收藏
页码:322 / 326
页数:5
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