Effects of the biological backbone on stacking interactions at DNA-protein interfaces: the interplay between the backbone•••π and π•••π components

The (gas-phase) MP2/6-31G*(0.25) pi center dot center dot center dot pi stacking interactions between the five natural bases and the aromatic amino acids calculated using (truncated) monomers composed of conjugated rings and/or (extended) monomers containing the biological backbone (either the protein backbone or deoxyribose sugar) were previously compared. Although preliminary energetic results indicated that the protein backbone strengthens, while the deoxyribose sugar either strengthens or weakens, the interaction calculated using truncated models, the reasons for these effects were unknown. The present work explains these observations by dissecting the interaction energy of the extended complexes into individual backbone center dot center dot center dot pi and pi center dot center dot center dot pi components. Our calculations reveal that the total interaction energy of the extended complex can be predicted as a sum of the backbone center dot center dot center dot pi and pi center dot center dot center dot pi components, which indicates that the biological backbone does not significantly affect the ring system through pi-polarization. Instead, we find that the backbone can indirectly affect the magnitude of the pi center dot center dot center dot pi contribution by changing the relative ring orientations in extended dimers compared with truncated dimers. Furthermore, the strengths of the individual backbone center dot center dot center dot pi contributions are determined to be significant (up to 18 kJ mol(-1)). Therefore, the origin of the energetic change upon model extension is found to result from a balance between an additional (attractive) backbone center dot center dot center dot pi component and differences in the strength of the pi center dot center dot center dot pi interaction. In addition, to understand the effects of the biological backbone on the stacking interactions at DNA-protein interfaces in nature, we analyzed the stacking interactions found in select DNA-protein crystal structures, and verified that an additive approach can be used to examine the strength of these interactions in biological complexes. Interestingly, although the presence of attractive backbone center dot center dot center dot pi contacts is qualitatively confirmed using the quantum theory of atoms in molecules (QTAIM), QTAIM electron density analysis is unable to quantitatively predict the additive relationship of these interactions. Most importantly, this work reveals that both the backbone center dot center dot center dot pi and pi center dot center dot center dot pi components must be carefully considered to accurately determine the overall stability of DNA-protein assemblies.