Abstract
The design, synthesis, and DNA binding properties of azaHx-PI or p-anisyl-4-aza-benzimidazole-pyrrole-imidazole (5) are described. AzaHx, 2-(p-anisyl)-4-aza-benzimidazole-5-carboxamide, is a novel, fluorescent DNA recognition element, derived from Hoechst 33258 to recognize G·C base pairs. Supported by theoretical data, the results from DNase I footprinting, CD, ΔT(M), and SPR studies provided evidence that an azaHx/IP pairing, formed from antiparallel stacking of two azaHx-PI molecules in a side-by-side manner in the minor groove, selectively recognized a C-G doublet. AzaHx-PI was found to target 5'-ACGCGT-3', the Mlu1 Cell Cycle Box (MCB) promoter sequence with specificity and significant affinity (K(eq) 4.0±0.2×10(7) M(-1)).
Keywords:
AzaHx; DNA; Distamycin; Hoechst 33258; Hx-amides; Minor groove; Polyamides; Sequence recognition.
Copyright © 2015 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Antigens, Neoplasm / genetics
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Antigens, Neoplasm / metabolism
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Base Pairing
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Benzimidazoles / chemical synthesis
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Benzimidazoles / chemistry*
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Benzimidazoles / metabolism
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Binding Sites
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Chemistry Techniques, Synthetic
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Circular Dichroism
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DNA / chemistry
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DNA / metabolism*
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DNA Topoisomerases, Type II / genetics
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DNA Topoisomerases, Type II / metabolism
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DNA-Binding Proteins / genetics
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DNA-Binding Proteins / metabolism
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Deoxyribonuclease I / chemistry
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Drug Design
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Fluorescent Dyes / chemistry*
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Fluorescent Dyes / metabolism
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Nylons / chemical synthesis
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Nylons / chemistry*
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Promoter Regions, Genetic
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Pyrroles / chemical synthesis
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Pyrroles / chemistry*
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Pyrroles / metabolism
Substances
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Antigens, Neoplasm
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Benzimidazoles
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DNA-Binding Proteins
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Fluorescent Dyes
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Nylons
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Pyrroles
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p-anisyl-4-aza-benzimidazole-pyrrole-imidazole
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DNA
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Deoxyribonuclease I
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DNA Topoisomerases, Type II