Add time:08/16/2019         Source:sciencedirect.com

The examination of a key series of chromophore analogues of sandramycin (cas 100940-65-6) (1) is detailed employing surface plasmon resonance to establish binding constants within a single high affinity bis-intercalation binding site 5′-d(GCATGC)2, and to establish the preference for sandramycin binding to 5′-d(GCXXGC)2 where XX=AT, TA, GC, and CG. From the latter studies, sandramycin was found to exhibit a preference that follows the order: 5′-d(GCATGC)2>5′-d(GCGCGC)2, ΔΔG°=0.4 kcal/mol>5′-d(GCTAGC)2, ΔΔG°=0.9 kcal/mol≥5′-d(GCCGGC)2, ΔΔG°=1.0 kcal/mol although it binds with high affinity to all four deoxyoligonucleotides. The two highest affinity sequences constitute repeating 5′-PuPy motifs with each intercalation event occurring at a 5′-PyPu step. The most effective sequence constitutes the least stable duplex, contains the sterically most accessible minor groove central to the bis-intercalation site, and the ability to accept two gly-NH/T C2 carbonyl H-bonds identified in prior NMR studies. Similarly, the contribution of the individual structural features of the chromophore were assessed with the high affinity duplex sequence 5′-d(GCATGC)2. In addition to the modest affinity differences, one of the most distinguishing features of the high affinity versus lower affinity bis-intercalation or mono-intercalation directly observable by surface plasmon resonance was the temporal stability of the complexes characterized by the exceptionally slow off-rates. ©

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