Intramolecularly stapled amphipathic peptides: Via a boron-sugar interaction

Article abstract of DOI:10.1039/d0cc02603d

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 into various positions of the peptide chain were investigated using high-resolution mass spectrometry (HR-MS), circular dichroism (CD), and nuclear magnetic resonance (NMR). This journal is

Full text of DOI:10.1039/d0cc02603d

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Czerwinska, S. Harthi, G. Woczaski, M. Waliczek, A. Emwas, M. Jaremko, L. Jaremko, P. Stefanowicz and
Z. Szewczuk, Chem. Commun., 2020, DOI: 10.1039/D0CC02603D.
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ISSN 1359-7345
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S. J. Connon, M. O. Senge et al.
Conformational control of nonplanar free base porphyrins:
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