Noncovalent interactions of amino acids with fullerene C60: A dispersion-corrected DFT study

By using the general gradient approximation functional PBE with Grimme's empirical dispersion correction in conjunction with the double numerical basis set DNP, we studied the noncovalent interaction of twenty proteinogenic l-amino acids (AAs) with fullerene C-60. The calculations were performed both under vacuum conditions and in aqueous medium. We analyzed the calculated geometries and binding energies for AA+C-60 complexes, the shape of HOMO and LUMO orbitals and the corresponding gap energies. Generally, we found a poor correlation between binding energies calculated for AA+C-60 complexes in aqueous medium and hydrophobicity scales proposed by other other authors. Despite of C-60 cage can be envisioned as a typical hydrophobic surface, the AA adsorption apparently takes place according to a mechanism different from classical hydrophobic interactions, or due to a combination of several types of interactions with a limited contribution of hydrophobic mechanism.