Bhattacharya, Santanu and Thomas, Mini (2000) Facile synthesis of oligopeptide distamycin analogs devoid of hydrogen bond donors or acceptors at the N-terminus: sequence-specific duplex DNA binding as a function of peptide chain length. In: Tetrahedron Letters, 41 (29). pp. 5571-5575.
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The first examples of distamycin analogs, which lack hydrogen bond interactor groups at the N-terminus, have been synthesized. The bispyrrole peptide did not exhibit any detectable binding with double-stranded (ds) DNA. However, all other homologues did bind to ds-DNA strongly, with the binding affinities increasing as a function of the number of repeating pyrrole carboxamide units, implying that a hydrogen bond donor or acceptor atom per se at the N-terminus is not essential for their DNA binding. Studies with poly d(GC) showed that the N-terminal formamide is not a prerequisite for GC binding, contrary to earlier postulations.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to Elsevier Science Ltd|
|Keywords:||Molecular Genetics;Biochemistry and Molecular Biophysics;Methods and Techniques;Pharmacology|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||17 Oct 2007|
|Last Modified:||19 Sep 2010 04:40|
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