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6 protocols using ara atp

1

RNA Primer and Nucleotide Synthesis Protocol

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All RNA primers and templates used for in this study were 5′-phosphorylated and purchased from Dharmacon (Lafayette, CO). 2′-CMe-ATP, RDV-TP, and SOF-TP were provided by Gilead Sciences (Foster City, CA). Ara-ATP, 2′deoxy-2′fluoro-CTP was purchased from TriLink (San Diego, CA). Ribavirin-TP was purchased from Jena Bioscience (Jena, Germany). Favipiravir-TP was purchased from Toronto Research Chemicals (North York, Ontario, Canada). NTPs and dATP were purchased from GE Healthcare. [α-32P]GTP was purchased from PerkinElmer Life Sciences.
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2

Synthesis and Purification of Modified Nucleotides

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ATP, UTP, CTP, GTP, 3′-dUTP, 3′-dATP, 3′-dGTP, 3′-dCTP, 2′-dATP, 2′-dCTP, 2′-dGTP, 2′-dTTP, 2′-F-CTP, 2′-F-GTP, 2′-NH2-GTP, 2′-NH2-CTP, 2′-F-ATP, 2′-F-UTP, ara-GTP, ara-ATP, 7-deaza-ATP, ara-CTP, ara-UTP, 2′-azido-GTP, and 2′-azido-CTP were purchased as 100 mM solutions from TriLink Biotechnologies (San Diego, CA). 2′-C-ethynyl-7-deaza-ATP was purchased from Carbosynth (San Diego, CA). Urea, taurine, dithiothreitol (DTT), imidazole, MgCl2, and IPTG (isopropyl-β-d-thiogalactopyranoside) were purchased from Sigma (St. Louis, MO). LB medium, bovine serum albumin (BSA), NaCl, Triton X-100, glycerol, protease inhibitor cocktail, Tris-HCl (pH 7.5), and HisPur Ni-NTA agarose resin were purchased from Thermo Fisher Scientific (Waltham, MA). An In-Fusion HD cloning kit and Stellar competent cells were purchased from Clontech (Mountain View, CA). The pMal-c5X vector was purchased from New England Bioscience (NEB; Ipswich, MA). Fluorescently labeled RNA (Cy5.5-RNA) and unlabeled DNA oligonucleotides were chemically synthesized and purified by high-performance liquid chromatography by Integrated DNA Technologies (Coralville, IA). 2′-C-Me-ATP, 2′-C-Me-GTP, 2′-F-2′-C-Me-GTP, 4′-azido-GTP, 2′-F-2′-C-Me-CTP, 2′-C-Me-CTP, 4′-azido-CTP, 2′-F-2′-C-Me-UTP, 2′-C-Me-UTP, 2′-C-ethynyl-UTP, and 4′-azido-UTP were custom synthesized in-house.
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3

Modified Nucleotides for RNA Synthesis

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The following nucleotides were purchased from Jena Bioscience: 5-ethynyl-UTP, 2-aminopurine-ribonucleotide-5′-triphosphate, 2′-O-methyl-CTP, 2′-O-methyl-ATP, ara-CTP, ara-ATP, ϵ-ATP, 2′-fluoro-ATP, 2′-fluoro-CTP, 2′-fluoro-UTP and 2′-fluoro-GTP.
The following ones were purchased from Trilink Biotechnologies: 5-methyl-UTP, ATP, CTP, UTP, GTP.
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4

RNA Primer and Reagent Sourcing

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All RNA primers and templates used in this study were purchased from Dharmacon (Lafayette, CO, USA). 2′C-methyl-ATP and remdesivir-TP were chemically synthesized by Gilead Sciences (Foster City, CA, USA). Ara-ATP was purchased from TriLink (San Diego, CA, USA). NTPs were purchased from GE Healthcare (Cranbury, NJ, USA).
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5

Evaluating Modified Nucleotide Incorporation

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Modified nucleotides, 3′-dATP (Cordycepin), 2′-amino-ATP, 2′-azido-ATP, araATP and 2′-O-methyl-ATP were from Trilink Biotechnologies, TNP–ATP was from Invitrogen, and LNA–ATP was from Jena Biosciences. The 50mer DNA primer/ 67mer DNA template was created as described above. For each modified nucleotide incorporation reaction, a 100  μL reaction mix was prepared containing 1× ThermoPol Buffer, 10 nM primer-template, 25 nM wild-type WT PolD or PolD H931A and 1  μM modified nucleotide. Reactions were incubated for 0, 1 or 15 min at 65°C and 10  μl aliquots were removed and mixed with 50 mM EDTA to quench the reaction. Reaction products were analyzed by capillary electrophoresis as described above. The concentration of product (51 nt DNA with a FAM label) was graphed for each nucleotide. All assays were performed in triplicate to ensure experiment reproducibility.
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6

RNA Primer and Nucleotide Synthesis

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All RNA primers and templates used in this study were 5′-phosphorylated and
purchased from Dharmacon (Lafayette, CO). 2′C-methyl-ATP (2′CM-ATP) and
RDV-TP were from Gilead Sciences (Foster City, CA). Ara-ATP was purchased from TriLink
(San Diego, CA). NTPs were purchased from GE Healthcare. [α-32P]-GTP was
purchased from PerkinElmer.
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