sFIDA automation yields sub-femtomolar limit of detection for Aβ aggregates in body fluids

Publication date: March 2017
Source:Clinical Biochemistry, Volume 50, Issues 4–5
Author(s): Yvonne Herrmann, Andreas Kulawik, Katja Kühbach, Maren Hülsemann, Luriano Peters, Tuyen Bujnicki, Kateryna Kravchenko, Christina Linnartz, Johannes Willbold, Christian Zafiu, Oliver Bannach, Dieter Willbold
ObjectivesAlzheimer's disease (AD) is a neurodegenerative disorder with yet non-existent therapeutic and limited diagnostic options. Reliable biomarker-based AD diagnostics are of utmost importance for the development and application of therapeutic substances. We have previously introduced a platform technology designated ‘sFIDA’ for the quantitation of amyloid β peptide (Aβ) aggregates as AD biomarker. In this study we implemented the sFIDA assay on an automated platform to enhance robustness and performance of the assay.Design and methodsIn sFIDA (surface-based fluorescence intensity distribution analysis) Aβ species are immobilized by a capture antibody to a glass surface. Aβ aggregates are then multiply loaded with fluorescent antibodies and quantitated by high resolution fluorescence microscopy. As a model system for Aβ aggregates, we used Aβ-conjugated silica nanoparticles (Aβ-SiNaPs) diluted in PBS buffer and cerebrospinal fluid, respectively. Automation of the assay was realized on a liquid handling system in combination with a microplate washer.ResultsThe automation of the sFIDA assay results in improved intra-assay precision, linearity and sensitivity in comparison to the manual application, and achieved a limit of detection in the sub-femtomolar range.ConclusionsAutomation improves the precision and sensitivity of the sFIDA assay, which is a prerequisite for high-throughput measurements and future application of the technology in routine AD diagnostics.

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