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High‐capacity protein A affinity chromatography for the fast quantification of antibodies: Two‐wavelength detection expands linear range
The high‐throughput analysis of antibodies from processes can be enhanced when the linear range is expanded and sample preparation is kept to a minimum. We developed a fast chromatography method based on a hexameric variant of staphylococcal protein A immobilized on Toyopearl matrix, TSK 5 PW using...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947708/ https://www.ncbi.nlm.nih.gov/pubmed/29330912 http://dx.doi.org/10.1002/jssc.201701481 |
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author | Satzer, Peter Jungbauer, Alois |
author_facet | Satzer, Peter Jungbauer, Alois |
author_sort | Satzer, Peter |
collection | PubMed |
description | The high‐throughput analysis of antibodies from processes can be enhanced when the linear range is expanded and sample preparation is kept to a minimum. We developed a fast chromatography method based on a hexameric variant of staphylococcal protein A immobilized on Toyopearl matrix, TSK 5 PW using two wavelengths. A protocol with 5 min runtime and a single‐wavelength detection at 280 nm yielded an upper limit of quantification of 2.10 mg/mL and a lower limit of quantification of 0.06 mg/mL. The optimized method with a runtime of 2 min and two‐wavelength detection at 280 and 300 nm allowed us to span a valid concentration range of 0.01–5.20 mg/mL using two calibration curves. Sample selectivity was tested using mock supernatant mixed with antibody concentrations of 0.1–2.1 mg/mL, sample stability in the autosampler was shown for at least 24 h. We also tested the capabilities of the method to determine purity of an antibody sample by calculating the ratio of peak area of elution to peak area of flow‐through, which correlated well with the expected purity. The method will be very useful for process development and in‐process control, spanning concentrations from seed fermentation to harvest and purification. |
format | Online Article Text |
id | pubmed-5947708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59477082018-05-17 High‐capacity protein A affinity chromatography for the fast quantification of antibodies: Two‐wavelength detection expands linear range Satzer, Peter Jungbauer, Alois J Sep Sci Liquid Chromatography The high‐throughput analysis of antibodies from processes can be enhanced when the linear range is expanded and sample preparation is kept to a minimum. We developed a fast chromatography method based on a hexameric variant of staphylococcal protein A immobilized on Toyopearl matrix, TSK 5 PW using two wavelengths. A protocol with 5 min runtime and a single‐wavelength detection at 280 nm yielded an upper limit of quantification of 2.10 mg/mL and a lower limit of quantification of 0.06 mg/mL. The optimized method with a runtime of 2 min and two‐wavelength detection at 280 and 300 nm allowed us to span a valid concentration range of 0.01–5.20 mg/mL using two calibration curves. Sample selectivity was tested using mock supernatant mixed with antibody concentrations of 0.1–2.1 mg/mL, sample stability in the autosampler was shown for at least 24 h. We also tested the capabilities of the method to determine purity of an antibody sample by calculating the ratio of peak area of elution to peak area of flow‐through, which correlated well with the expected purity. The method will be very useful for process development and in‐process control, spanning concentrations from seed fermentation to harvest and purification. John Wiley and Sons Inc. 2018-02-07 2018-04 /pmc/articles/PMC5947708/ /pubmed/29330912 http://dx.doi.org/10.1002/jssc.201701481 Text en © 2018 The Authors. Journal of Separation Science Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Liquid Chromatography Satzer, Peter Jungbauer, Alois High‐capacity protein A affinity chromatography for the fast quantification of antibodies: Two‐wavelength detection expands linear range |
title | High‐capacity protein A affinity chromatography for the fast quantification of antibodies: Two‐wavelength detection expands linear range |
title_full | High‐capacity protein A affinity chromatography for the fast quantification of antibodies: Two‐wavelength detection expands linear range |
title_fullStr | High‐capacity protein A affinity chromatography for the fast quantification of antibodies: Two‐wavelength detection expands linear range |
title_full_unstemmed | High‐capacity protein A affinity chromatography for the fast quantification of antibodies: Two‐wavelength detection expands linear range |
title_short | High‐capacity protein A affinity chromatography for the fast quantification of antibodies: Two‐wavelength detection expands linear range |
title_sort | high‐capacity protein a affinity chromatography for the fast quantification of antibodies: two‐wavelength detection expands linear range |
topic | Liquid Chromatography |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947708/ https://www.ncbi.nlm.nih.gov/pubmed/29330912 http://dx.doi.org/10.1002/jssc.201701481 |
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