Non-covalent interactions play an important role in chemistry, physics and especially in biodisciplines. They determine the structure of biomacromolecules such as DNA and proteins and are responsible for the molecular recognition process. Theoretical evaluation of interaction energies is difficult; however, perturbation as well as variation (supermolecular) methods are briefly described. Accurate interaction energies can be obtained by complete basis set limit calculations providing a large portion of correlation energy is covered (e.g. by performing CCSD(T) calculations). The role of H-bonding and stacking interactions in the stabilisation of DNA, oligopeptides and proteins is described, and the importance of London dispersion energy is shown.

Institute of Organic Chemistry and Biochemistry Academy of Sciences of the Czech Republic

References provided by Crossref.org

On the similar spectral manifestations of protonic and hydridic hydrogen bonds despite their different origin

Stacking interactions between carbohydrate and protein quantified by combination of theoretical and experimental methods