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Binding geometries of triple helix selective benzopyrido (4,3‐b)indole ligands complexed with double‐ and triple‐helical polynucleotides

Binding geometries of triple helix selective benzopyrido (4,3‐b)indole ligands complexed with... 10.1002/(SICI)1097-0282(199707)42:1<101::AID-BIP9>3.3.CO;2-T The binding modes of three benzopyrido (4,3‐b)indole derivatives (and one benzo(‐f)pyrido (4‐3b) quinoxaline derivative) with respect to double helical poly(dA) · poly(dT) and poly(d(A‐T))2 and triple‐helical poly(dA) · 2poly(dT) have been investigated using linear dichroism (LD) and CD: (I) 3‐methoxy‐11‐amino‐BePI where BePI = (7H‐8‐methyl‐benzo(e)pyrido (4,3‐b)indole), (II) 3‐methoxy‐11‐((3′‐amino) propylamino)‐BePI, (III) 3‐methoxy‐7‐((3′‐diethylamino)propylamino) BgPI where BgPI = (benzo(g)pyrido(4,3‐b)indole), and (IV) 3‐methoxy‐11‐((3′‐amino)propylamino) B f P Q where B f P Q = {benzo(‐f)pyrido(4‐3b)quinoxaline}. The magnitudes of the reduced LD of the electronic transitions of the polynucleotide bases and of the bound ligands are generally very similar, suggesting an orientation of the plane of the ligands' fused‐ring systems preferentially perpendicular to the helix axis. The LD results suggest that all of the ligands are intercalated for all three polynucleotides. The induced CD spectrum of the BePI chromophore in the (II‐BePI)‐poly(d(A‐T))2 complex is almost a mirror image of that for the (I‐BePI)‐poly(dA) · poly(dT) and (I‐BePI)‐poly(dA) · 2poly(dT) complexes, suggesting an antisymmetric orientation of the BePI moiety upon intercalation in poly(d(A‐T))2 compared to the other polynucleotides. The induced CD of I‐BePI bound to poly(dA) · 2poly(dT) suggests a geometry that is intermediate between that of its other two complexes. The concluded intercalative binding as well as the conformational variations between the different BePI complexes are of interest in relation to the fact that BePI derivatives are triplex stabilizers. © 1997 John Wiley & Sons, Inc. Biopoly 42: 101–111, 1997 http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Biopolymers Wiley

Binding geometries of triple helix selective benzopyrido (4,3‐b)indole ligands complexed with double‐ and triple‐helical polynucleotides

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References (35)

Publisher
Wiley
Copyright
Copyright © 1997 John Wiley & Sons, Inc.
ISSN
0006-3525
eISSN
1097-0282
DOI
10.1002/(SICI)1097-0282(199707)42:1<101::AID-BIP9>3.0.CO;2-S
Publisher site
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Abstract

10.1002/(SICI)1097-0282(199707)42:1<101::AID-BIP9>3.3.CO;2-T The binding modes of three benzopyrido (4,3‐b)indole derivatives (and one benzo(‐f)pyrido (4‐3b) quinoxaline derivative) with respect to double helical poly(dA) · poly(dT) and poly(d(A‐T))2 and triple‐helical poly(dA) · 2poly(dT) have been investigated using linear dichroism (LD) and CD: (I) 3‐methoxy‐11‐amino‐BePI where BePI = (7H‐8‐methyl‐benzo(e)pyrido (4,3‐b)indole), (II) 3‐methoxy‐11‐((3′‐amino) propylamino)‐BePI, (III) 3‐methoxy‐7‐((3′‐diethylamino)propylamino) BgPI where BgPI = (benzo(g)pyrido(4,3‐b)indole), and (IV) 3‐methoxy‐11‐((3′‐amino)propylamino) B f P Q where B f P Q = {benzo(‐f)pyrido(4‐3b)quinoxaline}. The magnitudes of the reduced LD of the electronic transitions of the polynucleotide bases and of the bound ligands are generally very similar, suggesting an orientation of the plane of the ligands' fused‐ring systems preferentially perpendicular to the helix axis. The LD results suggest that all of the ligands are intercalated for all three polynucleotides. The induced CD spectrum of the BePI chromophore in the (II‐BePI)‐poly(d(A‐T))2 complex is almost a mirror image of that for the (I‐BePI)‐poly(dA) · poly(dT) and (I‐BePI)‐poly(dA) · 2poly(dT) complexes, suggesting an antisymmetric orientation of the BePI moiety upon intercalation in poly(d(A‐T))2 compared to the other polynucleotides. The induced CD of I‐BePI bound to poly(dA) · 2poly(dT) suggests a geometry that is intermediate between that of its other two complexes. The concluded intercalative binding as well as the conformational variations between the different BePI complexes are of interest in relation to the fact that BePI derivatives are triplex stabilizers. © 1997 John Wiley & Sons, Inc. Biopoly 42: 101–111, 1997

Journal

Biopolymers – Wiley

Published: Jul 1, 1997

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