Pregled bibliografske jedinice broj: 1273049
Potential Clinically Relevant Effects of Sialylation on Human Serum AAG-Drug Interactions Assessed by Isothermal Titration Calorimetry: Insight into Pharmacoglycomics?
Potential Clinically Relevant Effects of Sialylation on Human Serum AAG-Drug Interactions Assessed by Isothermal Titration Calorimetry: Insight into Pharmacoglycomics? // International Journal of Molecular Sciences, 24 (2023), 10; 8472, 13 doi:10.3390/ijms24108472 (međunarodna recenzija, članak, znanstveni)
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Naslov
Potential Clinically Relevant Effects of
Sialylation on Human Serum AAG-Drug Interactions
Assessed by Isothermal Titration Calorimetry:
Insight into Pharmacoglycomics?
Autori
Kerep, Robert ; Šeba, Tino ; Borko, Valentina ; Weitner, Tin ; Keser, Toma ; Lauc, Gordan ; Gabričević, Mario
Izvornik
International Journal of Molecular Sciences (1422-0067) 24
(2023), 10;
8472, 13
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
alpha-1 acid glycoprotein ; drugs ; plasma protein binding ; sialic acid ; binding affinity ; isothermal titration calorimetry
Sažetak
Human serum alpha-1 acid glycoprotein is an acute- phase plasma protein involved in the binding and transport of many drugs, especially basic and lipophilic substances. It has been reported that the sialic acid groups that terminate the N–glycan chains of alpha-1 acid glycoprotein change in response to certain health conditions and may have a major impact on drug binding to alpha-1 acid glycoprotein. The interaction between native or desialylated alpha-1 acid glycoprotein and four representative drugs—clindamycin, diltiazem, lidocaine, and warfarin—was quantitatively evaluated using isothermal titration calorimetry. The calorimetry assay used here is a convenient and widely used approach to directly measure the amount of heat released or absorbed during the association processes of biomolecules in solution and to quantitatively estimate the thermodynamics of the interaction. The results showed that the binding of drugs with alpha-1 acid glycoprotein were enthalpy-driven exothermic interactions, and the binding affinity was in the range of 10−5–10−6 M. Desialylated alpha-1 acid glycoprotein showed significantly different binding with diltiazem, lidocaine, and warfarin compared with native alpha-1 acid glycoprotein, whereas clindamycin showed no significant difference. Therefore, a different degree of sialylation may result in different binding affinities, and the clinical significance of changes in sialylation or glycosylation of alpha-1 acid glycoprotein in general should not be neglected.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
GENOS d.o.o.
Profili:
Valentina Borko
(autor)
Mario Gabričević
(autor)
Tino Šeba
(autor)
Robert Kerep
(autor)
Gordan Lauc
(autor)
Tin Weitner
(autor)
Toma Keser
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE