Thermal stability of G-rich anti-parallel DNA triplexes upon insertion of LNA and α-l-LNAElectronic supplementary information (ESI) available. See DOI: 10.1039/c5ob00535c

• Main Authors: Kosbar, Tamer R, Sofan, Mamdouh A, Abou-Zeid, Laila, Pedersen, Erik B
• Format: Article
• Language: English
• ISSN: 1477-0520; 1477-0539
• DOI: 10.1039/c5ob00535c

G-rich anti-parallel DNA triplexes were modified with LNA or α- l -LNA in their Watson-Crick and TFO strands. The triplexes were formed by targeting a pyrimidine strand to a putative hairpin formed by Hoogsteen base pairing in order to use the UV melting method to evaluate the stability of the triplexes. Their thermal stability was reduced when the TFO strand was modified with LNA or α- l -LNA. The same trend was observed when the TFO strand and the purine Watson-Crick strand both were modified with LNA. When all triad components were modified with α- l -LNA and LNA in the middle of the triplex, the thermal melting was increased. When the pyrimidine sequence was modified with a single insertion of LNA or α- l -LNA the Δ T m increased. Moreover, increasing the number of α- l -LNA in the pyrimidine target sequence to six insertions, leads to a high increase in the thermal stability. The conformational S-type structure of α- l -LNA in anti-parallel triplexes is preferable for triplex stability. G-rich anti-parallel DNA triplexes were modified with LNA or α- l -LNA in their Watson-Crick and TFO strands.