Aldehyde oxidase assay by capillary electrophoresis: From off-line, online up to immobilized enzyme reactor
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
China Scholarship Council
GA19-08358S
Czech Science Foundation
PubMed
32627385
DOI
10.1002/jssc.202000412
Knihovny.cz E-zdroje
- Klíčová slova
- aldehyde oxidase, capillary electrophoresis, enzyme immobilization, magnetic nanoparticles, micellar electrokinetic chromatography,
- MeSH
- aldehydoxidasa analýza metabolismus MeSH
- elektroforéza kapilární MeSH
- enzymatické testy * MeSH
- enzymy imobilizované analýza metabolismus MeSH
- teplota MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- aldehydoxidasa MeSH
- enzymy imobilizované MeSH
Capillary electrophoresis is a modern separation technique characterized by many benefits, which qualify it also for enzyme assays and the study of enzyme kinetics during drug development. Homogeneous or heterogeneous approaches can be followed for the enzymatic incubation. In this study, an immobilization procedure of aldehyde oxidase on magnetic particles was developed considering their integration with capillary electrophoresis. A number of magnetic nano/microparticle types were tested for this purpose, showing that aldehyde oxidase was most active when immobilized on bare silica magnetic nanoparticles. Primarily, the reusability of the enzyme immobilized on bare silica nanoparticles was tested. Three consecutive incubations with substrate could be performed, but the activity considerably dropped after the first incubation. One reason could be an enzyme detachment from the nanoparticles, but no release was detected neither at 4°C nor at 37°C during 5 h. The drop in enzymatic activity observed in consecutive incubations, could also be due to inactivation of the enzyme over time at given temperature. For the immobilized enzyme stored at 4°C, the activity decreased to 83% after 5 h, in contrast with a steep decrease at 37°C to 37%.
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