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DNA structural features responsible for sequence‐dependent binding geometries of Hoechst 33258
Author(s) -
Moon JinHee,
Kim Seog K.,
Sehlstedt Ulrica,
Rodger Alison,
Nordén Bengt
Publication year - 1996
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/(sici)1097-0282(199605)38:5<593::aid-bip5>3.0.co;2-n
Subject(s) - chemistry , sequence (biology) , dna , computational biology , biophysics , stereochemistry , microbiology and biotechnology , biochemistry , biology
The complexes of Hoechst 33258 with poly[d(A‐T) 2 ], poly[d(I‐C) 2 ], poly[d(G‐C) 2 ], and poly[d(G‐m 5 C) 2 ] were studied using linear dichroism, CD, and fluorescence spectroscopies. The Hoechst‐poly[d(I‐C) 2 ] complex, in which there is no guanine amino group protruding in the minor groove, exhibits spectroscopic properties that are very similar to those of the Hoechst‐poly[d(A‐T) 2 ] complex. When bound to both of these polynucleotides, Hoechst exhibits an average orientation angle of near 45° relative to the DNA helix axis for the long‐axis polarized low‐energy transition, a relatively strong positive induced CD, and a strong increase in fluorescence intensity—leading us to conclude that this molecule also binds in the minor groove of poly[d(I‐C) 2 ]. By contrast, when bound to poly[d(G‐C) 2 ] and poly[d(G‐m 5 C) 2 ], Hoechst shows a distinctively different behavior. The strongly negative reduced linear dichroism in the ligand absorption region is consistent with a model in which part of the Hoechst chromophore is intercalculated between DNA bases. From the low drug:base ratio onset of excitonic effects in the CD and fluorescence emission spectra, it is inferred that another part of the Hoechst molecule may sit in the major groove of poly[d(G‐C) 2 ] and poly[d(G‐m 5 C) 2 ] and preferentially stacks into dimers, though this tendency is strongly reduced for the latter polynucleotide. Based on these results, the importance of the interactions of Hoechst with the exocyclic amino group of guanine and the methyl group of cytosine in determining the binding modes are discussed. © 1996 John Wiley & Sons, Inc.