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The molecular structure of the complex of Hoechst 33258 and the DNA dodecamer d(CGCGAATTCGCG)

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TLDR
The crystal structure of the complex between the dodecamer d(CGCGAATTCGCG) and a synthetic dye molecule Hoechst 33258 was solved by X-ray diffraction analysis and refined to an R-factor of 15.7% at 2.25 A resolution.
Abstract
The crystal structure of the complex between the dodecamer d(CGCGAATTCGCG) and a synthetic dye molecule Hoechst 33258 was solved by X-ray diffraction analysis and refined to an R-factor of 15.7% at 2.25 A resolution. The crescent-shaped Hoechst compound is found to bind to the central four AATT base pairs in the narrow minor groove of the B-DNA double helix. The piperazine ring of the drug has its flat face almost parallel to the aromatic bisbenzimidazole ring and lies sideways in the minor groove. No evidence of disordered structure of the drug is seen in the complex. The binding of Hoechst to DNA is stabilized by a combination of hydrogen bonding, van der Waals interaction and electrostatic interactions. The binding preference for AT base pairs by the drug is the result of the close contact between the Hoechst molecule and the C2 hydrogen atoms of adenine. The nature of these contacts precludes the binding of the drug to G-C base pairs due to the presence of N2 amino groups of guanines. The present crystal structural information agrees well with the data obtained from chemical footprinting experiments.

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Investigations on DNA intercalation and surface binding by SYBR Green I, its structure determination and methodological implications

TL;DR: Biophysical studies at defined dye/base pair ratios revealed the occurrence of intercalation, followed by surface binding at dbprs above approximately 0.15, and the structure-property relationships help in the design of methods that use SG, in particular dsDNA quantification in solution and real-time PCR.
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Dynamics of water in biological recognition.

TL;DR: Almost all biological macromoleculess proteins and DNAs are inactive in the absence of water, and the role of hydration in enzyme catalysis is well known and has recently been reviewed in a number of publications.
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A Simple, High-Resolution Method for Establishing DNA Binding Affinity and Sequence Selectivity

TL;DR: Techniques for establishing binding constants from quantitative titrations are compared, and recommendations are made for use of a Scatchard or curve fitting analysis of the titration binding curves as a reliable means to quantitate the binding affinity.
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Criteria for the mode of binding of DNA binding agents.

TL;DR: Comparative fluorescence and hydrodynamic studies using the proven intercalator ethidium and the groove binder Hoechst 33258 demonstrate reliable criteria that may be used to distinguish intercalation from groove binding in the absence of high resolution structural data.
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