Intramolecularly stapled amphipathic peptides: Via a boron-sugar interaction

Monika Kijewska; Angelika Czerwińska; Samah Al-Harthi; Grzegorz Wołczański; Mateusz Waliczek; Abdul Hamid Emwas; Mariusz Jaremko; Łukasz Jaremko; Piotr Stefanowicz; Zbigniew Szewczuk

doi:10.1039/d0cc02603d

Intramolecularly stapled amphipathic peptides: Via a boron-sugar interaction

Monika Kijewska
, Angelika Czerwińska
, Samah Al-Harthi
, Grzegorz Wołczański
, Mateusz Waliczek
, Abdul Hamid Emwas
, Mariusz Jaremko
, Łukasz Jaremko
, Piotr Stefanowicz
, Zbigniew Szewczuk

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

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

Original language	English (US)
Pages (from-to)	8814-8817
Number of pages	4
Journal	Chemical Communications
Volume	56
Issue number	62
DOIs	https://doi.org/10.1039/d0cc02603d
State	Published - Aug 11 2020
Externally published	Yes

ASJC Scopus subject areas

Electronic, Optical and Magnetic Materials
Catalysis
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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10.1039/d0cc02603d

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title = "Intramolecularly stapled amphipathic peptides: Via a 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 into various positions of the peptide chain were investigated using high-resolution mass spectrometry (HR-MS), circular dichroism (CD), and nuclear magnetic resonance (NMR).",

author = "Monika Kijewska and Angelika Czerwi{\'n}ska and Samah Al-Harthi and Grzegorz Wo{\l}cza{\'n}ski and Mateusz Waliczek and Emwas, \{Abdul Hamid\} and Mariusz Jaremko and {\L}ukasz Jaremko and Piotr Stefanowicz and Zbigniew Szewczuk",

note = "Publisher Copyright: {\textcopyright} The Royal Society of Chemistry.",

year = "2020",

month = aug,

day = "11",

doi = "10.1039/d0cc02603d",

language = "English (US)",

volume = "56",

pages = "8814--8817",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "62",

}

TY - JOUR

T1 - Intramolecularly stapled amphipathic peptides

T2 - Via a boron-sugar interaction

AU - Kijewska, Monika

AU - Czerwińska, Angelika

AU - Al-Harthi, Samah

AU - Wołczański, Grzegorz

AU - Waliczek, Mateusz

AU - Emwas, Abdul Hamid

AU - Jaremko, Mariusz

AU - Jaremko, Łukasz

AU - Stefanowicz, Piotr

AU - Szewczuk, Zbigniew

PY - 2020/8/11

Y1 - 2020/8/11

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

UR - https://www.scopus.com/pages/publications/85089162004

UR - https://www.scopus.com/pages/publications/85089162004#tab=citedBy

U2 - 10.1039/d0cc02603d

DO - 10.1039/d0cc02603d

M3 - Article

C2 - 32627786

AN - SCOPUS:85089162004

SN - 1359-7345

VL - 56

SP - 8814

EP - 8817

JO - Chemical Communications

JF - Chemical Communications

IS - 62

ER -

Intramolecularly stapled amphipathic peptides: Via a boron-sugar interaction

Abstract

ASJC Scopus subject areas

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