2022
Development of lectin arrays for mapping the glycosylation changes in proteins and cells
KOMÁREK, Jan, Marek KORSÁK, Lukáš FALTINEK a Michaela WIMMEROVÁZákladní údaje
Originální název
Development of lectin arrays for mapping the glycosylation changes in proteins and cells
Autoři
KOMÁREK, Jan (203 Česká republika, domácí), Marek KORSÁK (703 Slovensko, domácí), Lukáš FALTINEK (203 Česká republika, domácí) a Michaela WIMMEROVÁ (203 Česká republika, garant, domácí)
Vydání
XXIst Meeting of Biochemists and Molecular Biologists, 2022
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
10608 Biochemistry and molecular biology
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14310/22:00129422
Organizační jednotka
Přírodovědecká fakulta
ISBN
978-80-280-0136-0
Klíčová slova česky
lektiny, glykosylace, lektinové čipy
Klíčová slova anglicky
lectins; glycosylation; lectin arrays
Změněno: 6. 3. 2023 14:13, Mgr. Jan Komárek, Ph.D.
Anotace
V originále
Saccharides are essential for life, and in addition to their traditional roles as structural and energy storage components, they play crucial roles in many recognition events, signaling, and communication processes. The glycosylation of cells reflects the biological species, tissue, and physiological state of the organism. Importantly, changes in glycosylation patterns were observed in various tumors, and the aberrant glycosylation is often associated with malignancy potential, tumor immune surveillance, and patients´ prognosis. Lectin arrays are widely used tools for analyzing glycosylation in proteins and cells. They utilize a panel of lectins (saccharide-binding proteins with distinct sugar specificities) immobilized onto a solid surface. Lectin arrays allow for rapid and high-throughput glycomic analysis with minimal sample consumption. They can be used for glycan profiling of various samples, including purified glycoproteins, cell/tissue lysates, membrane vesicles, complex biological samples, or entire cells. This talk will present the development of customized lectin arrays in two different formats. The classical array in the microscope slide format was prepared by non-contact piezo dispensing of lectins onto a functionalized glass slide and their immobilization using various surface chemistries (immobilization on epoxy groups, NHS/EDC coupling). In the slide format, binding of glycosylated samples was detected by fluorescence measurement. To allow label-free detection of attached glyco-samples, lectin microarray prepared on bio-layer interferometry (BLI) sensor tips is currently being optimized. The fabricated lectin arrays will be used to map the glycosylation changes at different stages of cell differentiation and under different physiopathological conditions.
Návaznosti
GA21-29622S, projekt VaV |
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