Ab initio calculations on Pro-Ala and Pro-Gly dipeptides

Abstract

The geometries of the dipeptides l-Pro- l-Ala, l-Pro- d-Ala and l-Pro-Gly were investigated by a grid scan ab initio calculation. The 6-31G basis set was used to estimate the effect of the alanyl side-chain on the conformation of the peptide backbone and to provide a computational basis for the interpretation of known physical-chemical properties of larger peptides that contain these dipeptides. These calculations furnish a direct quantum mechanical assessment of the energetic consequences of a methyl side-chain in the i + 2 position of a turn. The results of the calculation support the current view that the presence of a d-Ala residue in the i + 2 position favors a type II β-turn over a type I β-turn conformation, while l-Ala has the opposite effect. Total and relative energies for all the optimized conformations identified by the grid search are given and geometric parameters (bond lengths, bond angles and dihedral angles) and net atomic charges have been calculated.