A series of oligomers containing alternate l-Ala and pGlu (pyroglutamic acid) both in the L and D form have been prepared and conformationally investigated by X-ray, NMR, UV/ECD, IR/VCD and molecular modelling. X-ray diffraction analysis was possible for the shortest oligomers LL-1 and LD-1. Molecular dynamics simulations of the oligomers demonstrated that the energy landscapes of the LL-series are broad. In contrast, the energy landscapes of the LD-series are characterized by well-defined minima corresponding to specific conformational structures. A single well-defined minimum exists in the energy landscape of the largest oligomer LD-8, corresponding to a precise conformation, characterized by i + 5 → i N-H⋯OC hydrogen bonds, typical of a π-helix. ECD and VCD spectra were measured to identify the chiroptical profiles of the oligomers. The most striking element in the ECD spectra of the LD-series is their exceptionally strong intensity, which confirms that these polypeptides attain a high degree of helical order. VCD spectra for the LD-series are well reproduced by frequency calculations when π-helix folds are employed as input structures, suggesting that a symmetrical VCD couplet around 1720 cm-1 can be taken as the VCD signature of π-helices.

Di Silvio S., Bologna F., Milli L., Giuri D., Zanna N., Castellucci N., et al. (2020). Elusive π-helical peptide foldamers spotted by chiroptical studies. ORGANIC & BIOMOLECULAR CHEMISTRY, 18(5), 865-877 [10.1039/c9ob02313e].

Elusive π-helical peptide foldamers spotted by chiroptical studies

Bologna F.;Milli L.;Giuri D.;Zanna N.;Castellucci N.;Monari M.;Calvaresi M.;Tomasini C.;
2020

Abstract

A series of oligomers containing alternate l-Ala and pGlu (pyroglutamic acid) both in the L and D form have been prepared and conformationally investigated by X-ray, NMR, UV/ECD, IR/VCD and molecular modelling. X-ray diffraction analysis was possible for the shortest oligomers LL-1 and LD-1. Molecular dynamics simulations of the oligomers demonstrated that the energy landscapes of the LL-series are broad. In contrast, the energy landscapes of the LD-series are characterized by well-defined minima corresponding to specific conformational structures. A single well-defined minimum exists in the energy landscape of the largest oligomer LD-8, corresponding to a precise conformation, characterized by i + 5 → i N-H⋯OC hydrogen bonds, typical of a π-helix. ECD and VCD spectra were measured to identify the chiroptical profiles of the oligomers. The most striking element in the ECD spectra of the LD-series is their exceptionally strong intensity, which confirms that these polypeptides attain a high degree of helical order. VCD spectra for the LD-series are well reproduced by frequency calculations when π-helix folds are employed as input structures, suggesting that a symmetrical VCD couplet around 1720 cm-1 can be taken as the VCD signature of π-helices.
2020
Di Silvio S., Bologna F., Milli L., Giuri D., Zanna N., Castellucci N., et al. (2020). Elusive π-helical peptide foldamers spotted by chiroptical studies. ORGANIC & BIOMOLECULAR CHEMISTRY, 18(5), 865-877 [10.1039/c9ob02313e].
Di Silvio S.; Bologna F.; Milli L.; Giuri D.; Zanna N.; Castellucci N.; Monari M.; Calvaresi M.; Gorecki M.; Angelici G.; Tomasini C.; Pescitelli G....espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/784618
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