Pregled bibliografske jedinice broj: 309242
Quantitative Protein Biomarker Analysis using Monolithic ImmunoDisks
Quantitative Protein Biomarker Analysis using Monolithic ImmunoDisks // Summer School on Monolith Technology for Biochromatography, Bioconversion, and Solid Phase Synthesis
Portorož, Slovenija, 2006. (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 309242 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Quantitative Protein Biomarker Analysis using Monolithic ImmunoDisks
Autori
Y.P. Lim, M. Ručević.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
Summer School on Monolith Technology for Biochromatography, Bioconversion, and Solid Phase Synthesis
Mjesto i datum
Portorož, Slovenija, 28.05.2006. - 31.05.2006
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
Inter-alpha inhibitor; Granzym K; Protein biomarker; Sepsis; Monolithic ImmunoDisks
Sažetak
Immunoassays are analytical methods based on signal responses generated as a consequence of an antibody-antigen reaction. Since they were first reported, immunoassays have witnessed phenomenal growth in the range and scope of their applications. A vast array of different labels and assay strategies has been developed to meet requirements of sensitivity, accuracy and convenience in analysis of biomolecules. They are widely used in such important areas as diagnostic biomarkers for various disease states and for assessment of progression or regression during therapy intervention as well as in drug development to provide important information about the safety and efficacy of candidate drugs. While conventional immunoassay such as enzyme-linked immunosorbant assays (ELISA) needs multiple reagents or labels, we attempt to develop a simple and rapid chromatographic based assay using monolithic CIM disks. We are currently investigating the roles of Inter-alpha inhibitor (IaI) and its physiological substrate, Granzyme K (GrK) in the pathogenesis of systemic inflammation/sepsis. The levels of these molecules in plasma of patients with sepsis were significantly altered compared to healthy individuals. Moreover, the plasma levels of IaI and GrK seem to correlate with the severity of the disease, suggesting the potential clinical utilization as useful predictive markers. Specific antibody reagents generated against IaI and GrK are immobilized on Epoxy-activated CIM minidisks to capture these molecules directly from plasma. Standard curves are developed by using known amounts of affinity purified IaI and GrK. Analysis of both biomarkers is performed separately or in tandem for simultaneous measurement of multiple circulating plasma biomarkers as a model for multiplex immunoassay. CIM ImmunoDisks provide a rapid and simple analysis of biomarkers in clinical arena as well as in clinical drug development.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti, Biotehnologija
POVEZANOST RADA
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb
Profili:
Marijana Ručević
(autor)