Effects of N-terminus substitution on the structure and spectroscopy of gas-phase helices

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Abstract

Because of the importance of helices in the secondary structure of proteins, we have undertaken a study of their spectroscopy, fragmentation patterns and conformations in the gas phase. In this work, we describe the effects of substitution at the N-terminus of polyalanine helices capped with a lysine at the C-terminus, namely Ac-Phe-(Ala)10-Lys-H+, Phe-(Ala)10-Lys-H+, and H+-Phe-(Ala) 10-Lys-H+. Acetylation of the N-terminus has very little effect on the spectroscopy and structure, but protonation of the N-terminus changes the infrared spectrum in such a way that we believe it may also change the structure of the peptide. The ultraviolet spectroscopy and fragmentation, on the other hand, are insensitive to either acetylation or protonation. © Schweizerische Chemische Gesellschaft.

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Stearns, J. A., Boyarkin, O. V., & Rizzo, T. R. (2008). Effects of N-terminus substitution on the structure and spectroscopy of gas-phase helices. In Chimia (Vol. 62, pp. 240–243). Swiss Chemical Society. https://doi.org/10.2533/chimia.2008.240

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