2′-Fluoronucleotides as substrates of viral replicative polymerases
Marina K. Kukhanova, А. Н. Коровина, Yu. A. Sharkin, Alex Azhayev, Sergey N. Kochetkov
Abstract
Marina K. Kukhanova, А. Н. Коровина, Yu. A. Sharkin, Alex Azhayev, Sergey N. Kochetkov
Abstract
Substrate specificities of three viral replicative polymerases of different origins (HIV reverse transcriptase, hepatitis C virus RNA polymerase, and herpes virus DNA polymerase) towards 2′F-NTP were studied. Activated DNA, polyA-oligoU 6 , and (2′F-A) 20 -oligoU 6 complexes were used as templates. It was shown that all DNA polymerases studied incorporate 2′F-NMP into the 3′-end of primer-template complexes. HIV reverse transcriptase and herpes virus DNA polymerase can elongate synthesis with both dNTP and 2′F-NTP. Homopolymer (2′F-A) 20 can serve as a template for the polymerization of UTP as well as 2′F-UTP catalyzed by hepatitis C virus polymerase although with the efficacy about five-to tenfold lower compared to the natural primer-template complex. The pyrophosphorolysis reaction of 2′F-CMP residue on the 3′-end of the primer catalyzed with HIV reverse transcriptase proceeds with an efficiency that is two orders of magnitude less compared to the natural dNMP residues in the same system.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Substrate specificities of three viral replicative polymerases of different origins (HIV reverse transcriptase, hepatitis C virus RNA polymerase, and herpes virus DNA polymerase) towards 2′F-NTP were studied. Activated DNA, polyA-oligoU 6 , and (2′F-A) 20 -oligoU 6 complexes were used as templates. It was shown that all DNA polymerases studied incorporate 2′F-NMP into the 3′-end of primer-template complexes. HIV reverse transcriptase and herpes virus DNA polymerase can elongate synthesis with both dNTP and 2′F-NTP. Homopolymer (2′F-A) 20 can serve as a template for the polymerization of UTP as well as 2′F-UTP catalyzed by hepatitis C virus polymerase although with the efficacy about five-to tenfold lower compared to the natural primer-template complex. The pyrophosphorolysis reaction of 2′F-CMP residue on the 3′-end of the primer catalyzed with HIV reverse transcriptase proceeds with an efficiency that is two orders of magnitude less compared to the natural dNMP residues in the same system.
Key concepts: Reverse transcriptase, Polymerase, Primer (cosmetics), DNA polymerase, Biology, DNA, Hepatitis B virus DNA polymerase, Molecular biology