Literature DB >> 32929962

Co(III)-NTA Mediated Antigen Immobilization on a Fiber Optic-SPR Biosensor for Detection of Autoantibodies in Autoimmune Diseases: Application in Immune-Mediated Thrombotic Thrombocytopenic Purpura.

Sara Horta1,2, Jia-Huan Qu2, Charlotte Dekimpe1, Quintijn Bonnez1, Aline Vandenbulcke1, Edwige Tellier3, Gilles Kaplanski3,4, Filip Delport5, Nick Geukens6, Jeroen Lammertyn2, Karen Vanhoorelbeke1,6.   

Abstract

Autoantibodies are key biomarkers in clinical diagnosis of autoimmune diseases routinely detected by enzyme-linked immunosorbent assays (ELISAs). However, the complexity of these assays is limiting their use in routine diagnostics. Fiber optic-surface plasmon resonance (FO-SPR) can overcome these limitations, but improved surface chemistries are still needed to guarantee detection of autoantibodies in complex matrices. In this paper, we describe the development of an FO-SPR immunoassay for the detection of autoantibodies in plasma samples from immune-mediated thrombotic thrombocytopenic purpura (iTTP) patients. Hereto, hexahistidine-tagged recombinant ADAMTS13 (rADAMTS13-His6) was immobilized on nitrilotriacetic acid (NTA)-coated FO probes chelated by cobalt (Co(III)) and exposed to anti-ADAMTS13 autoantibodies. Initial studies were performed to optimize rADAMTS13-His6 immobilization and to confirm the specificity of the immunoassay for detection of anti-ADAMTS13 autoantibodies with FO-SPR. The performance of the immunoassay was then evaluated by comparing Co(III)- and nickel (Ni(II))-NTA stabilized surfaces, confirming the stable immobilization of the antigen in Co(III)-NTA-functionalized FO probes. A calibration curve was prepared with a dilution series of a cloned human anti-ADAMTS13 autoantibody in ADAMTS13-depleted plasma resulting in an average interassay coefficient of variation of 7.1% and a limit of detection of 0.24 ng/mL. Finally, the FO-SPR immunoassay was validated using seven iTTP patient plasma samples, resulting in an excellent correlation with an in-house-developed ELISA (r = 0.973). In summary, the specificity and high sensitivity in combination with a short time-to-result (2.5 h compared to 4-5 h for a regular ELISA) make the FO-SPR immunoassay a powerful assay for routine diagnosis of iTTP and with extension for any other autoimmune disease.

Entities:  

Year:  2020        PMID: 32929962     DOI: 10.1021/acs.analchem.0c02586

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  3 in total

1.  A Fiber-Based SPR Aptasensor for the In Vitro Detection of Inflammation Biomarkers.

Authors:  Yu Hua; Ridong Wang; Dachao Li
Journal:  Micromachines (Basel)       Date:  2022-06-29       Impact factor: 3.523

Review 2.  Recent Advancements in Receptor Layer Engineering for Applications in SPR-Based Immunodiagnostics.

Authors:  Marcin Drozd; Sylwia Karoń; Elżbieta Malinowska
Journal:  Sensors (Basel)       Date:  2021-05-29       Impact factor: 3.576

3.  PfHRP2 detection using plasmonic optrodes: performance analysis.

Authors:  Médéric Loyez; Mathilde Wells; Stéphanie Hambÿe; François Hubinon; Bertrand Blankert; Ruddy Wattiez; Christophe Caucheteur
Journal:  Malar J       Date:  2021-07-28       Impact factor: 2.979

  3 in total

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