Local and cooperative structural transitions of double-stranded DNA in choline-based deep eutectic solvents

Int J Biol Macromol. 2024 Jan;256(Pt 2):128443. doi: 10.1016/j.ijbiomac.2023.128443. Epub 2023 Nov 28.

Abstract

The possibility of using deep eutectic solvents (DESs) as co-solvents for stabilizing and preserving the native structure of DNA provides an attractive opportunity in the field of DNA biotechnology. The rationale of this work is a systematic investigation of the effect of hydrated choline-based DES on the structural stability of a 30-base-pair double-stranded DNA model via a combination of spectroscopic experiments and MD simulations. UV absorption and CD experiments provide evidence of a significant contribution of DESs to the stabilization of the double-stranded canonical (B-form) DNA structure. Multi-wavelength synchrotron UV Resonance Raman (UVRR) measurements indicate that the hydration shell of adenine-thymine pairs is strongly perturbed in the presence of DESs and that the preferential interaction between H-bond sites of guanine residues and DESs is significantly involved in the stabilization of the dsDNA. Finally, MD calculations show that the minor groove of DNA is significantly selective for the choline part of the investigated DESs compared to the major groove. This finding is likely to have a significant impact not only in terms of thermal stability but also in the modulation of ligand-DNA interactions.

Keywords: Circular Dichroism; Deep eutectic solvents; Molecular dynamics simulation; Nucleic acids; Synchrotron UV Resonance Raman.

MeSH terms

  • Base Pairing
  • Choline* / chemistry
  • DNA
  • Deep Eutectic Solvents*
  • Solvents / chemistry

Substances

  • Deep Eutectic Solvents
  • Choline
  • Solvents
  • DNA