Table 1.
Tm [ΔTm/mod] (°C) |
|||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
ON | Duplex | B = | T | O | Q | S | V | W | X | Y | Z |
B1 | 5′-GBG ATA TGC | 28.5 | 31.0 | 26.5 | 20.0 | 17.5 | 35.5 | 38.5 | 39.0 | 29.0 | |
D2
|
3′-CAC TAT ACG |
|
|
[+2.5] |
[–2.0] |
[–8.5] |
[–11.0] |
[+7.0] |
[+10.0] |
[+10.5] |
[+0.5] |
B2 | 5′-GTG ABA TGC | 28.5 | 34.5 | 29.0 | 20.0 | 16.5 | 42.5 | 47.5 | 44.0 | 34.5 | |
D2
|
3′-CAC TAT ACG |
|
|
[+6.0] |
[+0.5] |
[–8.5] |
[–12.0] |
[+14.0] |
[+19.0] |
[+15.5] |
[+6.0] |
B3 | 5′-GTG ATA BGC | 28.5 | 31.5 | 27.5 | 16.5 | 14.5 | 39.0 | 42.5 | 40.0 | ND | |
D2
|
3′-CAC TAT ACG |
|
|
[+3.0] |
[–1.0] |
[–12.0] |
[–14.0] |
[+10.5] |
[+14.0] |
[+11.5] |
|
D1 | 5′-GTG ATA TGC | 28.5 | 32.0 | 28.0 | 17.0 | 12.0 | 35.0 | 39.0 | 38.5 | 29.0 | |
B4
|
3′-CAC BAT ACG |
|
|
[+3.5] |
[–0.5] |
[–11.5] |
[–16.5] |
[+6.5] |
[+10.5] |
[+10.0] |
[+0.5] |
D1 | 5′-GTG ATA TGC | 28.5 | 36.5 | 31.0 | 22.5 | 19.0 | 44.0 | 48.0 | 45.0 | 35.0 | |
B5
|
3′-CAC TAB ACG |
|
|
[+8.0] |
[+2.5] |
[–6.0] |
[–9.5] |
[+15.5] |
[+19.5] |
[+16.5] |
[+6.5] |
D1 | 5′-GTG ATA TGC | 28.5 | 36.0 | 27.5 | <10 | <10 | ND | 53.5 | 55.5 | ND | |
B6
|
3′-CAC BAB ACG |
|
|
[+3.8] |
[–0.5] |
|
|
|
[+12.5] |
[+13.5] |
|
B7 | 5′-GBG ABA BGC | 28.5 | 36.0 | 27.0 | <10 | <10 | ND | ND | 69.0 | ND | |
D2 | 3′-CAC TAT ACG | [+2.5] | [–0.5] | [+13.5] |
Thermal denaturation temperatures [Tm values/°C (ΔTm = change in Tm value calculated relative to D1:D2, D1:R2 and R1:D2 reference duplexes)] measured as the maximum of the first derivative of the melting curve (A260 vs temperature) recorded in medium salt buffer ([Na+] = 110 mM, [Cl–] = 100 mM, pH 7.0 (NaH2PO4/Na2HPO4)), using 1.0 μM concentrations of the two complementary strands. Tm values are averages of at least two measurements; A = adenin-9-yl DNA monomer, C = cytosin-1-yl DNA monomer, G = guanin-9-yl DNA monomer, T = thymin-1-yl DNA monomer, O = α-L-LNA thymin-1-yl monomer (Fig. 1). For structures of monomers Q-Z see Figure 1. ND = not determined.