Skip to main content
. Author manuscript; available in PMC: 2011 Jul 18.
Published in final edited form as: Chem Res Toxicol. 2007 Oct 4;20(12):1972–1979. doi: 10.1021/tx7002867

Table 2.

Thermal Melting Temperatures (Tm) of Oligonucleotide Duplexes Containing the N2-IQ Adduct

Oligonucleotides a TmTm)b,c
dGuo-N2-IQd dGuo-C8-IQe
a 5′-CTC GGC GCC ATC-3′ (12) 38° (−27°) 58° (−7°)
3′-GAG CCG CGG TAG-5′
b 5′-CTC GGC GCC ATC-3′ (13) 40° (−25°) 60° (−5°)
3′-GAG CCG CGG TAG-5′
c 5′-CTC GGC GCC ATC-3′ (14) 44° (−21°) 61° (−4°)
3′-GAG CCG CGG TAG-5′
d 5′-CTC GGC GCC ATC-3′ (14) 54° (+16°) 48° (+10°)
3′-GAG CCG --G TAG-5′
e 5′-G GCA GGT GGT G-3′ (15) 48° (−12°) 51° (−9°)
3′-C CGT CCA CCA C-5′
a

G is the modified dGuo.

b

ΔTm = Tm (modified) − Tm (unmodified). The Tm for the unmodified NarI duplex is 65 °C. The Tm for the unmodified NarI oligonucleotide opposite a two-base deletion (entry d) is 38 °C.

c

Conditions: 10 mM phosphate buffer (pH 7.0) containing 100 mM NaCl, 0.05 mM EDTA, and 0.5 A260/mL of each oligonucleotide. The temperature was raised 1 °C min−1.

d

This work.

e

Refs 30 and 31.