Subtle Recognition of 14-Base Pair DNA Sequences via Threading Polyintercalation
Author(s) -
Amy Smith,
Brian A. Ikkanda,
Garen G. Holman,
Brent L. Iverson
Publication year - 2012
Publication title -
biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.43
H-Index - 253
eISSN - 1520-4995
pISSN - 0006-2960
DOI - 10.1021/bi300317n
Subject(s) - threading (protein sequence) , dna , minor groove , base pair , dna footprinting , directionality , stereochemistry , binding site , molecule , antiparallel (mathematics) , chemistry , dissociation (chemistry) , dna binding site , deoxyribonuclease i , biophysics , crystallography , gene , dna binding protein , biology , genetics , biochemistry , base sequence , protein structure , gene expression , transcription factor , promoter , physics , organic chemistry , quantum mechanics , magnetic field
Small molecules that bind DNA in a sequence-specific manner could act as antibiotic, antiviral, or anticancer agents because of their potential ability to manipulate gene expression. Our laboratory has developed threading polyintercalators based on 1,4,5,8-naphthalene diimide (NDI) units connected in a head-to-tail fashion by flexible peptide linkers. Previously, a threading tetraintercalator composed of alternating minor-major-minor groove-binding modules was shown to bind specifically to a 14 bp DNA sequence with a dissociation half-life of 16 days [Holman, G. G., et al. (2011) Nat. Chem. 3, 875-881]. Herein are described new NDI-based tetraintercalators with a different major groove-binding module and a reversed N to C directionality of one of the minor groove-binding modules. DNase I footprinting and kinetic analyses revealed that these new tetraintercalators are able to discriminate, by as much as 30-fold, 14 bp DNA binding sites that differ by 1 or 2 bp. Relative affinities were found to correlate strongly with dissociation rates, while overall C(2) symmetry in the DNA-binding molecule appeared to contribute to enhanced association rates.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom