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Distinguishing the glycan isomers 2,3-sialyllactose and 2,6-sialyllactose by voltammetry after modification with osmium(VI) complexes
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SYSNO ASEP 0507731 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Distinguishing the glycan isomers 2,3-sialyllactose and 2,6-sialyllactose by voltammetry after modification with osmium(VI) complexes Author(s) Trefulka, Mojmír (BFU-R) RID, ORCID
Černocká, Hana (BFU-R) RID, ORCID
Fojt, Lukáš (BFU-R) RID, ORCID
Paleček, Emil (BFU-R) RID, ORCID
Ostatná, Veronika (BFU-R) RID, ORCIDNumber of authors 5 Source Title Analytica Chimica Acta. - : Elsevier - ISSN 0003-2670
Roč. 1067, AUG 27 2019 (2019), s. 56-62Number of pages 7 s. Publication form Print - P Language eng - English Country NL - Netherlands Keywords glycosylation ; strategies ; proteins ; oligosaccharides ; polysaccharides Subject RIV CB - Analytical Chemistry, Separation OECD category Analytical chemistry R&D Projects GA18-18154S GA ČR - Czech Science Foundation (CSF) Method of publishing Limited access Institutional support BFU-R - RVO:68081707 UT WOS 000466150300005 DOI 10.1016/j.aca.2019.03.060 Annotation Altered glycosylation is a universal feature of cancer cells and certain glycans are well-known markers of tumor progression. In this work we studied two glycan isomers, 2,3-sialyllactose (3-SL) and 2,6-sialyllactose (6-SL), frequently appearing in glycoproteins connected with cancer. A combination of square wave voltammetry and glycan modification with osmium(VI) N, N, N', N'-tetramethylethylenedi-amine (Os(VI) tem) allowed to distinguish between these regioisomers, since the 6-SL molecule can bind three Os(VI), while the 3-SL only two Os(VI) moieties, as experiments using capillary electrophoresis, inductively coupled plasma mass spectrometry and thin layer chromatography showed. A similar pattern of Os(VI)-modification was found for isomers of sialyl-N-acetyllactosamine and sialylgalactose. Covalent adducts of Os(VI) tem with glycans yielded three reduction voltammetric peaks. The ratio of peak I/peak II heights depends on the content of individual regioisomer in the sample. Our proposed approach allows the determination of isomer percentage representation in the mixture after one voltammogram recording. These results show a new appropriate method for the discrimination of glycan isomers containing terminal sialic acid important for distinguishing between cancerous and non-cancerous origin of biomarkers. (C) 2019 Elsevier B.V. All rights reserved. Workplace Institute of Biophysics Contact Jana Poláková, polakova@ibp.cz, Tel.: 541 517 244 Year of Publishing 2020 Electronic address https://www.sciencedirect.com/science/article/pii/S0003267019303782?via%3Dihub
Number of the records: 1