High-throughput quantitation of Fc-containing recombinant proteins in cell culture supernatant by fluorescence polarization spectroscopy

التفاصيل البيبلوغرافية
العنوان: High-throughput quantitation of Fc-containing recombinant proteins in cell culture supernatant by fluorescence polarization spectroscopy
المؤلفون: David C. James, Ben Thompson, Kalpana Nayyar, Mike Jenns, Ray Field, Jerry Clifford, Andrew Smith
المصدر: Analytical Biochemistry
سنة النشر: 2017
مصطلحات موضوعية: 0301 basic medicine, Biophysics, Cell Culture Techniques, Fluorescence Polarization, CHO Cells, 01 natural sciences, Biochemistry, law.invention, 03 medical and health sciences, Cricetulus, law, High-Throughput Screening Assays, Animals, Molecular Biology, Chromatography, biology, Chinese hamster ovary cell, 010401 analytical chemistry, Immunoglobulin Fc Fragments, Cell Biology, Recombinant Proteins, 0104 chemical sciences, Culture Media, Titer, 030104 developmental biology, Spectrometry, Fluorescence, Cell culture, biology.protein, Recombinant DNA, Antibody, human activities, Fluorescence anisotropy
الوصف: Measurement of recombinant protein product titer critically underpins all biopharmaceutical manufacturing process development, as well as diverse research and discovery activity. Here, we describe a simple rapid (2 min per 96 samples) 96-well microplate-based assay that enables high-throughput quantitation of recombinant immunoglobulin G and Fc-containing IgG derivatives in mammalian cell culture supernatant over a wide dynamic range of 2.5-80 mg/L, using microplate fluorescence polarization (FP) spectroscopy. The solution-phase FP assay is based on the detection of immunoglobulin Fc domain containing analyte binding to FITC-conjugated recombinant Protein G ligand to measure analyte concentration dependent changes in emitted FP. For ease of use and maximal shelf life, we showed that air-dried assay microplates containing pre-formulated ligand that is re-solubilized on addition of analyte containing solution did not affect assay performance, typically yielding an across plate coefficient of variation of1%, and a between-plate standard deviation below 1%. Comparative assays of the same samples by FP and other commonly used IgG assay formats operating over a similar dynamic range (Protein A HPLC and bio-interferometry) yielded a coefficient of determination0.99 in each case.
تدمد: 1096-0309
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef2d214240577d007d18fc3a72051de2
https://pubmed.ncbi.nlm.nih.gov/28716374
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....ef2d214240577d007d18fc3a72051de2
قاعدة البيانات: OpenAIRE