Abstract

Combined experimental-theoretical investigation of ultrafast hydration dynamics of an A-form RNA double helix in water reveals an ordered arrangement of water molecules and provides boundary conditions for the ion atmosphere around the polyanionic RNA.

Highlights

  • We report the first ultrafast pump-probe and 2D-IR study of an Ribonucleic acid (RNA) double helix in a water environment augmented by in depth theoretical modelling of the RNA vibrational response

  • The presence of an OH group attached to the 2’ position of the ribose units has a strong impact on the vibrational spectrum and the hydration pattern in which the phosphate and sugar groups serve as distinct interaction sites for water molecules

  • The action of the fluctuating electric force generated by low-frequency, e.g., librational motion of solvating water molecules is directly manifested in the vibrational lineshape of the backbone modes that report on local field fluctuations in the 2-3 neighboring water layers [1,2]

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Summary

Introduction

We report the first ultrafast pump-probe and 2D-IR study of an RNA double helix in a water environment augmented by in depth theoretical modelling of the RNA vibrational response. RNA backbone vibrational modes of phosphate and sugar groups in the frequency range 900-1300 cm-1 are utilized to monitor solvation dynamics and molecular couplings (Fig. 1).

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