Determination of DNA minor groove width in distamycin-DNA complexes by solid-state NMR

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Abstract

We have performed solid-state 31P-19F REDOR nuclear magnetic resonance (NMR) experiments to monitor changes in minor groove width of the oligo-nucleotide d(CGCAAA2′FUTGGC ·d(GCCAAT(pS)TTGCG) (A3T2) upon binding of the drug distamycin A at different stoichiometries. In the hydrated solid-state sample, the minor groove width for the unbound DNA, measured as the 2′FU7-pS19 inter-label distance, was 9.4 ± 0.7 Å, comparable to that found for similar A:T-rich DNAs. Binding of a single drug molecule is observed to cause a 2.4 Å decrease in groove width. Subsequent addition of a second drug molecule results in a larger conformational change, expanding this minor groove width to 13.6 Å, consistent with the results of a previous solution NMR study of the 2:1 complex. These 31P-19F REDOR results demonstrate the ability of solid-state NMR to measure distances of 7-14 Å in DNA-drug complexes and provide the first example of a direct spectroscopic measurement of minor groove width in nucleic acids.

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Olsen, G. L., Louie, E. A., Drobny, G. P., & Sigurdsson, S. T. (2003). Determination of DNA minor groove width in distamycin-DNA complexes by solid-state NMR. Nucleic Acids Research, 31(17), 5084–5089. https://doi.org/10.1093/nar/gkg720

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