AMP-α-F

(ApF)

Adenosine-5′-(α-fluoro)-monophosphate, Sodium salt

Adenosine-5′-(1-fluoro)-monophosphate, Sodium salt

For in vitro use only!

Shipping: shipped on gel packs

Storage Conditions: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible.

Shelf Life: 12 months after date of delivery

Molecular Formula: C₁₀H₁₃FN₅O₆P (free acid)

Molecular Weight: 349.21 g/mol (free acid)

Exact Mass: 349.06 g/mol (free acid)

CAS#: 19375-33-8 (free acid), 15503-75-0 (sodium salt)

Purity: ≥ 95 % (HPLC)

Form: solid

Color: white to off-white

Spectroscopic Properties: λ_max 259 nm, ε 15.4 L mmol^-1 cm^-1 (Tris-HCl pH 7.5)

Applications:
Substrate for snake venom phosphodiesterase ^[1,2]
Substrate for Fhit proteins ^[3]
Inhibitor of adenlyate kinase ^[4]

Selected References:
[1] Baranowski et al. (2016) A fluorescent HTS assay for phosphohydrolases based on nucleoside 5′-fluorophosphates: its application in screening for inhibitors of mRNA decapping scavenger and PDE-I. Org. Biomol. Chem. 14 (20):4595.
[2] Baranowski et al. (2015) Synthesis of fluorophosphate nucleotide analogues and their characterization as tools for ¹⁹F NMR studies. J. Org. Chem. 80 (8):3982.
[3] Guranowski et al. (2008) Fhit proteins can also recognize substrates other than dinucleoside polyphosphates. FEBS Lett. 582 (20):3152.
[4] Scoblov et al. (1996) Modified nucleotides as substrates and inhibitors of adenylate kinase from different sources. FEBS Lett. 395 (2-3):283.

Structural formula of AMP-α-F

m⁷GMP-α-F

(m⁷GpF)

7-Methyl-guanosine-5′-(α-fluoro)-monophosphate

7-Methyl-guanosine-5′-(1-fluoro)-monophosphate

For in vitro use only!

Shipping: shipped on gel packs

Storage Conditions: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible.

Shelf Life: 12 months after date of delivery

Molecular Formula: C₁₁H₁₅FN₅O₇P

Molecular Weight: 379.24 g/mol

Exact Mass: 379.07 g/mol

CAS#: 1698011-01-6 (inner salt)

Purity: ≥ 95 % (HPLC)

Form: solid

Color: white to off-white

Spectroscopic Properties: λ_max 258/280 nm, ε 9.8/8.0 L mmol^-1 cm^-1 (Tris-HCl pH 7.5)

Applications:
Substrate for human mRNA decapping scavenger enzyme ^[1,2]

Selected References:
[1] Baranowski et al. (2016) A fluorescent HTS assay for phosphohydrolases based on nucleoside 5′-fluorophosphates: its application in screening for inhibitors of mRNA decapping scavenger and PDE-I. Org. Biomol. Chem. 14 (20):4595.
[2] Baranowski et al. (2015) Synthesis of fluorophosphate nucleotide analogues and their characterization as tools for ¹⁹F NMR studies. J. Org. Chem. 80 (8):3982.

Structural formula of m⁷GMP-α-F

2-Fluoro-ATP

(2F-ATP)

2-Fluoro-adenosine-5′-triphosphate, Sodium salt

For research use only!

Shipping: shipped on gel packs

Storage Conditions: store at -20 °C
Short term exposure (up to 1 week cumulative) to ambient temperature possible.

Shelf Life: 12 months after date of delivery

Molecular Formula: C₁₀H₁₅N₅O₁₃P₃F (free acid)

Molecular Weight: 525.17 g/mol (free acid)

Exact Mass: 524.99 g/mol (free acid)

CAS#: 1492-62-2 (free acid)

Purity: ≥ 95 % (HPLC)

Form: solution in water

Color: colorless to slightly yellow

Concentration: 100 mM – 110 mM

pH: 7.5 ±0.5

Spectroscopic Properties: λ_abs 261 nm, ε 14.3 L mmol^-1 cm^-1 (Tris-HCl pH 7.5)

Description:
Figure 1A: Schematic representation of the secondary structure of the Gsw^apt. The stems are named in blue and the loops are named in green. All fluorinated bases are labeled in red.
Figure 1B: 10% PAA-Gel of the transcription samples containing from left to right: low range ssRNA-marker, transcription with unlabeled dNTPs, ¹⁵N-UTP, ¹⁵N-GTP, 2F-ATP, ¹⁵N-UTP-GTP + 2F-ATP.
Figure 1C: CD-melting curve of the Gsw^apt in the ligand bound state. The black curve represents the unlabeled RNA and the green curve represents the ¹⁹F-labeled RNA. The melting curves were recorded in the absence (left) and presence (right) of the ligand.
Figure 1D: ¹H-¹⁵N-HSQC of the Gsw^apt. The spectrum of the unlabeled RNA is shown on the top and the spectrum of the ¹⁹F-labeled RNA is shown at the bottom.

RNA Structure Determination by NMR with 2F-ATP

Application Note

By courtesy of

Florian Sochor, sochor@nmr.uni-frankfurt.de
and
Harald Schwalbe, schwalbe@nmr.uni-frankfurt.de

Goethe-Universität Frankfurt am Main,
Max-von-Laue-Straße 7, D-60438 Frankfurt am Main

Multidimensional NMR studies of RNAs are based on the correlation between magnetic properties of protons and of other NMR-active atoms. In nucleic acids these atoms are usually ¹³C, ¹⁵N and ³¹P. Whereas ³¹P is at 100% natural abundance, the other NMR-active, non-radioactive isotopes have low natural abundance. The methodic challenges are to artificially enrich or introduce NMR active isotopes of ¹³C and ¹⁵N into the molecules without affecting their overall structural integrity. Besides the atoms present in RNA, also introduction of different NMR reporter signals is of considerable interest in NMR studies of large RNAs.
In this application note we substituted the hydrogen at positions 2 in the base of adenosine (Ade-2H) with ¹⁹F, which has a comparable gyromagnetic ratio as ¹H but exhibits larger chemical shift dispersion. The Ade-2H position was chosen as the attached nucleus is spatially close enough to the base pairing but does not show J-coupling to other protons.

We introduce ¹⁹F labelling for the 73 nucleotides comprising RNA aptamer region of the guanine sensing riboswitch from Bacillus subtilis (Gsw^apt, shown in Fig 1A). Due to the inherent low sensitivity, samples of RNA for NMR spectroscopic studies require high concentration of the solute, in this case of the ¹⁹F labeled RNA. Therefore it was synthesized in large scale (0.15 mg) by in vitro transcription with 2F-ATP complementing ATP. The composition of the transcription mix is shown in Table 1. The concentrations of Mg(OAc)₂, DNA-template, nucleotides and YIPP were optimized for highest transcription efficiency. Several in vitro transcriptions with different nucleotide composition were performed overnight at 37 °C (Figure 1B). The yield of ¹⁹F labeled Gsw^apt synthesized within a transcription reaction containing also ¹⁵N-GTP and ¹⁵N-UTP was compared with the yield in a transcription reaction containing solely ¹⁵N-GTP and ¹⁵N-UTP as isotope labeled compounds. All NTP compositions led to a single 73 nt RNA product. The transcription efficiency, measured by HPLC, is 1.9% (±0.4%) for all transcriptions including 2F-ATP compared to 2.1% (±0.5%) for the transcriptions with unlabeled or ¹⁵N-labeled nucleotides only.