Antiparallel Side-by-Side Dimeric Motif for Sequence-Specific Recognition in the Minor Groove of DNA by the Designed Peptide 1-Methylimidazole-2 Carboxamide Netropsin

The designed peptide 1-methylimidazole-2-carboxamide netropsin (2-ImN) binds specifically to the sequence 5'-TGACT-3'. Direct evidence from NMR spectroscopy is presented that this synthetic ligand binds DNA as a 2:1 complex, which reveals that the structure is an antiparallel dimer in the...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1992-08, Vol.89 (16), p.7586-7590
Hauptverfasser: Mrksich, Milan, Wade, Warren S., Dwyer, Tammy J., Geierstanger, Bernhard H., Wemmer, David E., Dervan, Peter B.
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Sprache:eng
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Zusammenfassung:The designed peptide 1-methylimidazole-2-carboxamide netropsin (2-ImN) binds specifically to the sequence 5'-TGACT-3'. Direct evidence from NMR spectroscopy is presented that this synthetic ligand binds DNA as a 2:1 complex, which reveals that the structure is an antiparallel dimer in the minor groove of DNA. This is in contrast to the 1:1 complexes usually seen with most crescent-shaped minor groove binding molecules targeted toward A+T-rich tracts but reminiscent of a dimeric motif found for distamycin at high concentrations. These results suggest that sequence-dependent groove width may play an important role in allowing an expanded set of DNA binding motifs for synthetic peptides.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.89.16.7586