DNA TRIPLEX STABILIZATION USING A TETHERED MINOR-GROOVE BINDING HOECHST-33258 ANALOG

Citation
J. Robles et Lw. Mclaughlin, DNA TRIPLEX STABILIZATION USING A TETHERED MINOR-GROOVE BINDING HOECHST-33258 ANALOG, Journal of the American Chemical Society, 119(26), 1997, pp. 6014-6021
Citations number
44
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
119
Issue
26
Year of publication
1997
Pages
6014 - 6021
Database
ISI
SICI code
0002-7863(1997)119:26<6014:DTSUAT>2.0.ZU;2-5
Abstract
Tethering the Hoechst 33258 fluorophore to the 5'-terminus of the poly pyrimidine third strand of parallel-stranded DNA triplexes results in complexes with increased T-m, values that vary with both the pH of the solution and the sequence of the target DNA. These pH/sequence effect s are Likely related to the presence of M+-G-C base triplets, which ca n result in either charge-charge effects involving the base triplet an d the charged piperazine ring of the ligand or changes in the nature o f the minor groove binding site resulting from the introduction of the N-2-exocyclic amino group(s). As with DNA duplexes, sequence targets rich in A-T base pairs are most effective in taking advantage of such ligand-induced stability. A duplex sequence rich in A-T base pairs adj acent to the triple helix also appears to permit adjacent ligand bindi ng; that is, the tripler is stabilized by the binding of the tethered minor groove ligand in an A-T rich duplex adjacent to the site of the tripler. The Hoechst ligand can be very effective in stabilizing G-T-A base triplets which are generally less effective in tripler formation , presumably as the result of a single interstrand G-T hydrogen bond. Stabilization may occur in part because the (AATT)(2) minor groove may offer the ligand a preferred binding site as has been documented for this sequence in DNA duplexes. Binding to the tripler results in an en hanced quantum yield for the fluorophore, the magnitude of which is de pendent upon sequence effects. Stopped flow experiments have provided some insight into the nature of the process; rapid ligand binding to t he duplex target is followed by a slower process, one interpreted to r eflect the third strand binding to generate the conjugated DNA tripler . Although not conclusive, the experiments suggest that the Hoechst co njugated polypyrimidine strands bind to the target duplex by two simul taneous sets of interactions: (i) third strand binding in the major gr oove and (ii) tethered Hoechst 33258 ligand binding in the minor groov e.