8bna

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(New page: 200px<br /><applet load="8bna" size="350" color="white" frame="true" align="right" spinBox="true" caption="8bna, resolution 2.200&Aring;" /> '''BINDING OF HOECHST ...)
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==Overview==
==Overview==
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An X-ray crystallographic structure analysis has been carried out on the, complex between the antibiotic and DNA fluorochrome Hoechst 33258 and a, synthetic B-DNA dodecamer of sequence C-G-C-G-A-A-T-T-C-G-C-G. The drug, molecule, which can be schematized as:, phenol-benzimidazole-benzimidazole-piperazine, sits within the minor, groove in the A-T-T-C region of the DNA double helix, displacing the spine, of hydration that is found in drug-free DNA. The NH groups of the, benzimidazoles make bridging three-center hydrogen bonds between adenine, N-3 and thymine O-2 atoms on the edges of base-pairs, in a manner both, mimicking the spine of hydration and calling to mind the binding of the, auti-tumor drug netropsin. Two conformers of Hoechst are seen in roughly, equal populations, related by 180 degrees rotation about the central, benzimidazole-benzimidazole bond: one form in which the piperazine ring, extends out from the surface of the double helix, and another in which it, is buried deep within the minor groove. Steric clash between the drug and, DNA dictates that the phenol-benzimidazole-benzimidazole portion of, Hoechst 33258 binds only to A.T regions of DNA, whereas the piperazine, ring demands the wider groove characteristic of G.C regions. Hence, the, piperazine ring suggests a possible G.C-reading element for synthetic DNA, sequence-reading drug analogs.
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An X-ray crystallographic structure analysis has been carried out on the complex between the antibiotic and DNA fluorochrome Hoechst 33258 and a synthetic B-DNA dodecamer of sequence C-G-C-G-A-A-T-T-C-G-C-G. The drug molecule, which can be schematized as: phenol-benzimidazole-benzimidazole-piperazine, sits within the minor groove in the A-T-T-C region of the DNA double helix, displacing the spine of hydration that is found in drug-free DNA. The NH groups of the benzimidazoles make bridging three-center hydrogen bonds between adenine N-3 and thymine O-2 atoms on the edges of base-pairs, in a manner both mimicking the spine of hydration and calling to mind the binding of the auti-tumor drug netropsin. Two conformers of Hoechst are seen in roughly equal populations, related by 180 degrees rotation about the central benzimidazole-benzimidazole bond: one form in which the piperazine ring extends out from the surface of the double helix, and another in which it is buried deep within the minor groove. Steric clash between the drug and DNA dictates that the phenol-benzimidazole-benzimidazole portion of Hoechst 33258 binds only to A.T regions of DNA, whereas the piperazine ring demands the wider groove characteristic of G.C regions. Hence, the piperazine ring suggests a possible G.C-reading element for synthetic DNA sequence-reading drug analogs.
==About this Structure==
==About this Structure==
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Binding of Hoechst 33258 to the minor groove of B-DNA., Pjura PE, Grzeskowiak K, Dickerson RE, J Mol Biol. 1987 Sep 20;197(2):257-71. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=2445998 2445998]
Binding of Hoechst 33258 to the minor groove of B-DNA., Pjura PE, Grzeskowiak K, Dickerson RE, J Mol Biol. 1987 Sep 20;197(2):257-71. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=2445998 2445998]
[[Category: Protein complex]]
[[Category: Protein complex]]
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[[Category: Dickerson, R.E.]]
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[[Category: Dickerson, R E.]]
[[Category: Grzeskowiak, K.]]
[[Category: Grzeskowiak, K.]]
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[[Category: Pjura, P.E.]]
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[[Category: Pjura, P E.]]
[[Category: HT]]
[[Category: HT]]
[[Category: MG]]
[[Category: MG]]
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[[Category: double helix]]
[[Category: double helix]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jan 29 21:52:15 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 19:17:45 2008''

Revision as of 17:17, 21 February 2008


8bna, resolution 2.200Å

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BINDING OF HOECHST 33258 TO THE MINOR GROOVE OF B-DNA

Overview

An X-ray crystallographic structure analysis has been carried out on the complex between the antibiotic and DNA fluorochrome Hoechst 33258 and a synthetic B-DNA dodecamer of sequence C-G-C-G-A-A-T-T-C-G-C-G. The drug molecule, which can be schematized as: phenol-benzimidazole-benzimidazole-piperazine, sits within the minor groove in the A-T-T-C region of the DNA double helix, displacing the spine of hydration that is found in drug-free DNA. The NH groups of the benzimidazoles make bridging three-center hydrogen bonds between adenine N-3 and thymine O-2 atoms on the edges of base-pairs, in a manner both mimicking the spine of hydration and calling to mind the binding of the auti-tumor drug netropsin. Two conformers of Hoechst are seen in roughly equal populations, related by 180 degrees rotation about the central benzimidazole-benzimidazole bond: one form in which the piperazine ring extends out from the surface of the double helix, and another in which it is buried deep within the minor groove. Steric clash between the drug and DNA dictates that the phenol-benzimidazole-benzimidazole portion of Hoechst 33258 binds only to A.T regions of DNA, whereas the piperazine ring demands the wider groove characteristic of G.C regions. Hence, the piperazine ring suggests a possible G.C-reading element for synthetic DNA sequence-reading drug analogs.

About this Structure

8BNA is a Protein complex structure of sequences from [1] with and as ligands. Full crystallographic information is available from OCA.

Reference

Binding of Hoechst 33258 to the minor groove of B-DNA., Pjura PE, Grzeskowiak K, Dickerson RE, J Mol Biol. 1987 Sep 20;197(2):257-71. PMID:2445998

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