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Exploring the Conformational Preferences of 20-residue Peptides in Isolation: Ac-Ala19-Lys + H+ vs. Ac-Lys-Ala19 + H+ and the Current Reach of DFT

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Schubert, F.*; Rossi, M.; Baldauf, C.*; Pagel, K.; Warnke, S.; von Helden, G.; Filsinger, F.; Kupser, P.; Meijer, G.; Salwiczek, M.; Koksch, B.; Scheffler, M.; Blum, V.* – 2015

Reliable, quantitative predictions of the structure of peptides based on their amino-acid sequence information are an ongoing challenge. We here explore the energy landscapes of two unsolvated 20-residue peptides that result from a shift of the position of one amino acid in otherwise the same sequence. Our main goal is to assess the performance of current state-of-the-art density-functional theory for predicting the structure of such large and complex systems, where weak interactions such as dispersion or hydrogen bonds play a crucial role. For validation of the theoretical results, we employ experimental gas-phase ion mobility-mass spectrometry and IR spectroscopy. While unsolvated Ac-Ala19-Lys + H+ will be shown to be a clear helix seeker, the structure space of Ac-Lys-Ala19 + H+ is more complicated. Our first-principles structure-screening strategy using the dispersion-corrected PBE functional (PBE + vdWTS) identifies six distinctly different structure types competing in the low-energy regime (≈16 kJ mol−1). For these structure types, we analyze the influence of the PBE and the hybrid PBE0 functional coupled with either a pairwise dispersion correction (PBE + vdWTS, PBE0 + vdWTS) or a many-body dispersion correction (PBE + MBD*, PBE0 + MBD*). We also take harmonic vibrational and rotational free energy into account. Including this, the PBE0 + MBD* functional predicts only one unique conformer to be present at 300 K. We show that this scenario is consistent with both experiments.

Title
Exploring the conformational preferences of 20-residue peptides in isolation: Ac-Ala19-Lys + H+ vs. Ac-Lys-Ala19 + H+ and the current reach of DFT
Author
Schubert, F.*; Rossi, M.; Baldauf, C.*; Pagel, K.; Warnke, S.; von Helden, G.; Filsinger, F.; Kupser, P.; Meijer, G.; Salwiczek, M.; Koksch, B.; Scheffler, M.; Blum, V.*
Date
2015
Identifier
10.1039/C4CP05541A
Source(s)
Citation
Phys. Chem. Chem. Phys. 2015, 17, 7373-7385
Type
Text
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