Ganesh N.
Nawale
a,
Saeed
Bahadorikhalili
a,
Pallabi
Sengupta
b,
Sandeep
Kadekar
a,
Subhrangsu
Chatterjee
b and
Oommen P.
Varghese
*a
aTranslational Chemical Biology Laboratory, Division of Polymer Chemistry, Department of Chemistry-Ångström, Uppsala University, Uppsala, Sweden. E-mail: oommen.varghese@kemi.uu.se
bBiomolecular NMR and Drug Design Laboratory, Department of Biophysics, Bose Institute, P-1/12 CIT Scheme VII M, Kolkata, India
First published on 7th August 2019
Correction for ‘4′-Guanidinium-modified siRNA: a molecular tool to control RNAi activity through RISC priming and selective antisense strand loading’ by Ganesh N. Nawale et al., Chem. Commun., 2019, 55, 9112–9115.
Name | Passenger (5′–3′, above) and guide strand (3′–5′, below) | T m | ΔTmb/mod. |
---|---|---|---|
a T m represents melting temperatures for unmodified and GMU modified siRNA duplexes (bold text indicates modification) in °C. b ΔTm represents the [Tm (RNA mod.) − Tm (RNA unmod.)]. The Tm values were determined using 1 μM of siRNA in buffer containing 50 mM NaCl, 10 mM Na2PO4, pH 7.4. All experiments were triplicated, and the Tm values have reported an average of 3 measurements with the estimated standard deviation. | |||
siRNA1 | GGAAGCUGCAGAAAGAUACTT | 66.9 ± 0.1 | |
TTCCUUCGACGUCUUUCUAUG | |||
siRNA2 | GGAAGCUGCAGAAAGAUACTT | 67.8 ± 0.3 | +0.9 |
TTCCUUCGACGUCUUUCUAUG | |||
siRNA3 | GGAAGCUGCAGAAAGAUACTT | 69.8 ± 0.1 | +2.9 |
TTCCUUCGACGUCUUUCUAUG | |||
siRNA4 | GGAAGCUGCAGAAAGAUACTT | 69.5 ± 0.2 | +2.6 |
TTCCUUCGACGUCUUUCUAUG | |||
siRNA5 | GGAAGCUGCAGAAAGAUACTT | 69.7 ± 0.3 | +2.8 |
TTCCUUCGACGUCUUUCUAUG | |||
siRNA6 | GGAAGCUGCAGAAAGAUACTT | 70.3 ± 0.2 | +3.4 |
TTCCUUCGACGUCUUUCUAUG |
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
This journal is © The Royal Society of Chemistry 2019 |