Surface plasmon resonance biosensor for direct detection of antibody against Epstein-Barr virus
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
16797175
DOI
10.1016/j.bios.2006.04.021
PII: S0956-5663(06)00226-0
Knihovny.cz E-zdroje
- MeSH
- analýza selhání vybavení MeSH
- biosenzitivní techniky přístrojové vybavení metody MeSH
- design vybavení MeSH
- imunoanalýza přístrojové vybavení metody MeSH
- protilátky analýza imunologie MeSH
- virus Epsteinův-Barrové - jaderné antigeny analýza imunologie MeSH
- virus Epsteinův-Barrové imunologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- EBV-encoded nuclear antigen 1 MeSH Prohlížeč
- protilátky MeSH
- virus Epsteinův-Barrové - jaderné antigeny MeSH
This paper describes the direct label-free detection of antibodies against the Epstein-Barr virus (anti-EBNA) using a surface plasmon resonance (SPR) biosensor. The antibody detection was performed using the immunoreaction between anti-EBNA and a respective synthetic peptide (EBNA-1), which was conjugated with bovine serum albumin (BSA-EBNA) and immobilized on the sensor surface. Three immobilization chemistries for the attachment of BSA-EBNA were investigated to optimize ligand density and minimize loss of EBNA-1 immunoreactivity. The developed SPR biosensor functionalized with the optimal immobilization method was calibrated and characterized in terms of detection limit, reproducibility, regenerability and storability. It was demonstrated that the sensor is capable of detecting concentrations of anti-EBNA as low as 0.2 ng/ml (approximately 1 pM) both in buffer and 1% human serum and can be stored and regenerated for repeated use.
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