Literature DB >> 10873664

Enantiospecific recognition of DNA sequences by a proflavine Tröger base.

C Bailly1, W Laine, M Demeunynck, J Lhomme.   

Abstract

The DNA interaction of a chiral Tröger base derived from proflavine was investigated by DNA melting temperature measurements and complementary biochemical assays. DNase I footprinting experiments demonstrate that the binding of the proflavine-based Tröger base is both enantio- and sequence-specific. The (+)-isomer poorly interacts with DNA in a non-sequence-selective fashion. In sharp contrast, the corresponding (-)-isomer recognizes preferentially certain DNA sequences containing both A. T and G. C base pairs, such as the motifs 5'-GTT. AAC and 5'-ATGA. TCAT. This is the first experimental demonstration that acridine-type Tröger bases can be used for enantiospecific recognition of DNA sequences. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10873664     DOI: 10.1006/bbrc.2000.2997

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  1 in total

1.  Glycoconjugates Based on Supramolecular Tröger's Base Scaffold: Synthesis, Photophysics, Docking, and BSA Association Study.

Authors:  Débora Muller Pimentel Aroche; Jaqueline Pinto Vargas; Pablo Andrei Nogara; Fabiano da Silveira Santos; João Batista Teixeira da Rocha; Diogo Seibert Lüdtke; Fabiano Severo Rodembusch
Journal:  ACS Omega       Date:  2019-08-01
  1 in total

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