TY - JOUR
T1 - Intramolecularly stapled amphiphatic peptides via boron-sugar interaction
AU - Kijewska, Monika
AU - Czerwinska, Angelika
AU - Al-Harthi, Samah
AU - Wołczański, Grzegorz
AU - Waliczek, Mateusz
AU - Emwas, Abdul-Hamid M.
AU - Jaremko, Mariusz
AU - Jaremko, Lukasz
AU - Stefanowicz, Piotr
AU - Szewczuk, Zbigniew
N1 - KAUST Repository Item: Exported on 2020-10-01
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.
PY - 2020/6/23
Y1 - 2020/6/23
N2 - 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).
AB - 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).
UR - http://hdl.handle.net/10754/663873
UR - http://pubs.rsc.org/en/Content/ArticleLanding/2020/CC/D0CC02603D
U2 - 10.1039/d0cc02603d
DO - 10.1039/d0cc02603d
M3 - Article
C2 - 32627786
SN - 1359-7345
JO - Chemical Communications
JF - Chemical Communications
ER -