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5 protocols using adenosine triphosphate (atp)

1

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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2

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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3

In Vitro Transcription of mRNA from pT7TS Plasmid

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The pT7TS plasmid was linearized for 4 h with the restriction enzyme SmaI (Fermentas) as a DNA template for mRNA in vitro transcription. The linearized pT7TS DNA in 200 μL was recovered by precipitating it with 40 μL 5 M NaOAc (Invitrogen) and 480 μL 100% EtOH, followed by 30 min of chilling at −20°C. The linearized pT7TS DNA was washed twice with 1 mL 75% EtOH after being centrifuged at 15,000 rpm for 20 min at 4°C. Following air drying, pT7TS DNA was resuspended to 1 μg/μL in H2O (Sigma). A single in vitro transcription reaction of TS mRNA in 40 μL contained 1 μg pT7TS DNA as a template, 5 mM guanosine triphosphate, ATP, cytidine triphosphate, and N1-methyl-pseudoUTP (TriLink, San Diego), 4 mM CleanCap AG 3′Ome, 0.002 U/μL pyrophosphatase (Thermo Fisher Scientific), 1 U RNase inhibitor, and 10 U/μL T7 polymerase; the reaction was incubated for 90 min at 37°C. The TS mRNA was isolated from the in vitro transcription reaction by using a MegaClear RNA purification kit (Thermo Fisher Scientific) and resuspended in H2O for LNP preparation.
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4

In vitro Methylated RNA Synthesis

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Double-stranded DNA templates carrying T7 promoter were prepared by primer extension with two single-stranded DNA oligos (Supplementary Tables 5 and 6). Unmethylated and methylated E. coli tRNA (Arg2, CGT), RNA#1, and RNA#2 were synthesized by in vitro transcription using T7 RNA polymerase. ATP and N6-methyl-ATP (TriLink, N-1013) were supplied in the presence of UTP, CTP, and GTP to synthesize unmethylated and methylated RNA, respectively. RNA was purified by E.Z.N.A Micro RNA kits (Omega Bio-Tek, R7034) and quantified by NanoDrop One (Thermo Fisher Scientific).
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5

Synthesis of mRNA and miR-switches

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mRNAs and miR-switches were synthesized as previously described (Miki et al., 2015 (link); Warren et al., 2010 (link)). Briefly, they were generated with a MEGAscript T7 Transcription Kit (Ambion, cat. no. AMB13345) and a modified protocol. Template DNAs, T7 enzyme, ATP, guanosine triphosphate, pseudo-UTP (Tri-Link Bio Technologies, cat. no. N-1019-10), 5-methyl-CTP (Tri-Link Bio Technologies, cat. no. N-1014-10) and Anti Reverse Cap Analog (Tri-Link Bio Technologies, cat. no. N-7003-10) were reacted at 37 °C for 4 h. Adding TURBO DNase, the reacted products were further incubated at 37 °C for 30 min. The resulting mRNAs and miR-switches were incubated with Antarctic Phosphatase (New England Biolabs, cat. no. M0289S) at 37 °C for 30 min. The RNeasy MinElute Cleanup Kit (QIAGEN, cat. no. 74204) was used to purify the mRNAs and miR-switches.
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