Synthesis of Tetravalent Thio- and Selenogalactoside-Presenting Galactoclusters and Their Interactions with Bacterial Lectin PA-IL from Pseudomonas aeruginosa

• Autoři: ILLYÉS Tünde Zita; MALINOVSKÁ Lenka; RŐTH Erzsébet; TÓTH Boglárka; FARKAS Bence; KORSÁK Marek; WIMMEROVÁ Michaela; KÖVÉR Katalin E.; CSÁVÁS Magdolna
• Rok publikování: 2021
• Druh: Článek v odborném periodiku
• Časopis / Zdroj: Molecules
• Fakulta / Pracoviště MU: Přírodovědecká fakulta
• www: https://doi.org/10.3390/molecules26030542
• Doi: http://dx.doi.org/10.3390/molecules26030542
• Klíčová slova: selenoglycosides; galactoclusters; Pseudomonas aeruginosa; PA-IL lectin; multivalency
• Popis: Synthesis of tetravalent thio- and selenogalactopyranoside-containing glycoclusters using azide-alkyne click strategy is presented. Prepared compounds are potential ligands of Pseudomonas aeruginosa lectin PA-IL. P. aeruginosa is an opportunistic human pathogen associated with cystic fibrosis, and PA-IL is one of its virulence factors. The interactions of PA-IL and tetravalent glycoconjugates were investigated using hemagglutination inhibition assay and compared with mono- and divalent galactosides (propargyl 1-thio- and 1-seleno-beta-d-galactopyranoside, digalactosyl diselenide and digalactosyl disulfide). The lectin-carbohydrate interactions were also studied by saturation transfer difference NMR technique. Both thio- and seleno-tetravalent glycoconjugates were able to inhibit PA-IL significantly better than simple d-galactose or their intermediate compounds from the synthesis.

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