Intramolecularly stapled amphiphatic peptides via boron-sugar interaction

Abstract
Amadori products (deoxyfructosyllysine derivatives) that can selectively interact with phenylboronic acids and borate ions were synthesized. The intramolecular interactions between the fructosyl moiety and phenylboronic acid incorporated in various positions of peptide chain was investigated using high-resolution mass spectrometry (HR-MS), circular dichroism (CD), and nuclear magnetic resonance (NMR).

Citation
Kijewska, M., Czerwinska, A., Al-Harthi, S., Wołczański, G., Waliczek, M., Emwas, A.-H., … Szewczuk, Z. (2020). Intramolecularly stapled amphiphatic peptides via boron-sugar interaction. Chemical Communications. doi:10.1039/d0cc02603d

Acknowledgements
This work was supported by Grant No.UMO2015/19/B/ST5/00659 from the National Science Centre, Poland. The authors would like to thank Andrzej Reszka (ShimPol, Poland) for providing the Shimadzu LCMS-IT-TOF. LJ, MJ, SMA, and A-HE would like to thank the King Abdullah University of Science and Technology (KAUST) for financial support.

Publisher
Royal Society of Chemistry (RSC)

Journal
Chemical Communications

DOI
10.1039/d0cc02603d

Additional Links
http://pubs.rsc.org/en/Content/ArticleLanding/2020/CC/D0CC02603D

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