Assessment of Energy Effects Determining cis-trans Proline Isomerization in Dipeptides
Abstract
Herein, we present the results of molecular dynamics, potential of mean force (PMF) and quantum mechanical (QM) calculations aimed to investigate the cis-trans equilibria of short peptides: capped Ac-Z-NHMe, Ac-X-Z-NHMe, and zwitterionic Leu-Z with X = Gln, Leu, Tyr and Z = Pro, Ala. Both PMF free energies and average QM energies in aqueous solution consistently predict that the Ala → Pro substitution stabilizes the Ac/X-Z cis isomer in all the model compounds. Using the interacting quantum atoms method, we decomposed the average QM energies into physical components and performed a comparative analysis between the Pro-containing peptides and their Ala-substituted counterparts. The results point out that cis-trans isomerization is not controlled by a single steric or electronic contribution and unveil a mixture of electrostatic, steric and hyperconjugative effects that is modulated by the dipeptide sequence. It is also shown that solute-solvent interactions stabilize systematically the trans and cis isomer of the Ala- and Pro-containing capped peptides, respectively, suggesting thus that solvation plays a key role in the Pro cis effect observed in these systems in agreement with former proposals.
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