| Literature DB >> 2823885 |
K Kissinger1, K Krowicki, J C Dabrowiak, J W Lown.
Abstract
A series of monocationic lexitropsins, or information-reading oligopeptides, were synthesized to minimize and offset the AT bias for doubly cationic ligands bound in the minor groove of DNA. The compounds possess an N-formyl group in place of the guanidinium moiety normally present in netropsin. By systematic replacement of the N-methylpyrrole groups of the dipeptide with N-methylimidazole, a remarkably high degree of sequence specificity was obtained. One of the compounds having two N-methylimidazole residues was found to exhibit dramatically altered specificity when compared with netropsin and preferred to bind to the sequence 5'-CCGT-3' 3'-GGCA-5'. The structural elements underlying sequence recognition in terms of the model for the netropsin-DNA interaction are presented and discussed.Entities:
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Year: 1987 PMID: 2823885 DOI: 10.1021/bi00392a002
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162