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. Author manuscript; available in PMC: 2010 Apr 13.
Published in final edited form as: J Org Chem. 2009 Feb 6;74(3):1070–1081. doi: 10.1021/jo802037v

Table 4.

Energetics derived from thermal denaturation curves of duplexes between 2'-amino-α-L-LNA functionalized with non-aromatic moieties and DNA/RNA.a

Complementary DNA
Complementary RNA
ON Sequence ΔG298 [ΔΔG298] (kJ/mol) ΔH [ΔΔH] (kJ/mol) T298ΔS [Δ(T298ΔS)] (kJ/mol) ΔG298 [ΔΔG298] (kJ/mol) ΔH [ΔΔH] (kJ/mol) T298ΔS [Δ(T298ΔS)] (kJ/mol)
D1 5′-GTG ATA TGC –41 –327 –286 –38 –275 –237
O2 5′-GTG AOA TGC –46 [–5] –354 [–27] –308 [–22] –46 [–8] –361 [–86] –315 [–78]
Q2 5′-GTG AQA TGC –41 [0] –312 [+15] –271 [+15] –40 [–2] –302 [–27] –261 [–24]
S2 5′-GTG ASA TGC –33 [+8] –349 [–22] –316 [–30] –31 [+7] –352 [–77] –321 [–84]
V2 5′-GTG AVA TGC –29 [+12] –295 [+32] –266 [+20] –30 [+8] –303 [–28] –273 [–36]
a

Thermal denaturation curves were obtained as described in Tables 1 and 2. ΔΔG298, ΔΔH and Δ(T298ΔS) change in ΔG298, ΔH and Δ(T298ΔS) values, respectively, calculated relative to D1:D2 and D1:R2 reference duplexes). Values in italics indicate deviation from (or lack of) monomer trend. ND = not determined. See Table S6 for data from B1-B5 series.