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Precise determination of protein extinction coefficients under native and denaturing conditions using SV-AUC
The accurate determination of protein concentration is an important though non-trivial task during the development of a biopharmaceutical. The fundamental prerequisite for this is the availability of an accurate extinction coefficient. Common approaches for the determination of an extinction coeffic...
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Published in: | European biophysics journal 2018-10, Vol.47 (7), p.761-768 |
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description | The accurate determination of protein concentration is an important though non-trivial task during the development of a biopharmaceutical. The fundamental prerequisite for this is the availability of an accurate extinction coefficient. Common approaches for the determination of an extinction coefficient for a given protein are either based on the theoretical prediction utilizing the amino acid sequence or the photometric determination combined with a measurement of absolute protein concentration. Here, we report on an improved SV-AUC based method utilizing an analytical ultracentrifuge equipped with absorbance and Rayleigh interference optics. Global fitting of datasets helped to overcome some of the obstacles encountered with the traditional method employing synthetic boundary cells. Careful calculation of
dn/dc
values taking glycosylation and solvent composition into account allowed the determination of the extinction coefficients of monoclonal antibodies and an Fc-fusion protein under native as well as under denaturing conditions. An intra-assay precision of 0.9% and an accuracy of 1.8% compared to the theoretical value was achieved for monoclonal antibodies. Due to the large number of data points of a single dataset, no meaningful difference between the ProteomeLab XL-I and the new Optima AUC platform could be observed. Thus, the AUC-based approach offers a precise, convenient and versatile alternative to conventional methods like total amino acid analysis (AAA). |
doi_str_mv | 10.1007/s00249-018-1299-x |
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dn/dc
values taking glycosylation and solvent composition into account allowed the determination of the extinction coefficients of monoclonal antibodies and an Fc-fusion protein under native as well as under denaturing conditions. An intra-assay precision of 0.9% and an accuracy of 1.8% compared to the theoretical value was achieved for monoclonal antibodies. Due to the large number of data points of a single dataset, no meaningful difference between the ProteomeLab XL-I and the new Optima AUC platform could be observed. Thus, the AUC-based approach offers a precise, convenient and versatile alternative to conventional methods like total amino acid analysis (AAA).</description><identifier>ISSN: 0175-7571</identifier><identifier>EISSN: 1432-1017</identifier><identifier>DOI: 10.1007/s00249-018-1299-x</identifier><identifier>PMID: 29666888</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Amino acid sequence ; Amino acids ; Biochemistry ; Biological and Medical Physics ; Biomedical and Life Sciences ; Biopharmaceuticals ; Biophysics ; Cell Biology ; Coefficients ; Data points ; Fc receptors ; Fusion protein ; Glycosylation ; Life Sciences ; Membrane Biology ; Monoclonal antibodies ; Nanotechnology ; Neurobiology ; Optics ; Original Article ; Photometry ; Proteins</subject><ispartof>European biophysics journal, 2018-10, Vol.47 (7), p.761-768</ispartof><rights>European Biophysical Societies' Association 2018</rights><rights>European Biophysics Journal is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-4dd3cc97ec870acb8b35d1e10046cc0d497ad2e902fe2eaace51a5bee8f926b43</citedby><cites>FETCH-LOGICAL-c372t-4dd3cc97ec870acb8b35d1e10046cc0d497ad2e902fe2eaace51a5bee8f926b43</cites><orcidid>0000-0001-9392-0700</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29666888$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoffmann, Andreas</creatorcontrib><creatorcontrib>Grassl, Kerstin</creatorcontrib><creatorcontrib>Gommert, Janine</creatorcontrib><creatorcontrib>Schlesak, Christian</creatorcontrib><creatorcontrib>Bepperling, Alexander</creatorcontrib><title>Precise determination of protein extinction coefficients under native and denaturing conditions using SV-AUC</title><title>European biophysics journal</title><addtitle>Eur Biophys J</addtitle><addtitle>Eur Biophys J</addtitle><description>The accurate determination of protein concentration is an important though non-trivial task during the development of a biopharmaceutical. The fundamental prerequisite for this is the availability of an accurate extinction coefficient. Common approaches for the determination of an extinction coefficient for a given protein are either based on the theoretical prediction utilizing the amino acid sequence or the photometric determination combined with a measurement of absolute protein concentration. Here, we report on an improved SV-AUC based method utilizing an analytical ultracentrifuge equipped with absorbance and Rayleigh interference optics. Global fitting of datasets helped to overcome some of the obstacles encountered with the traditional method employing synthetic boundary cells. Careful calculation of
dn/dc
values taking glycosylation and solvent composition into account allowed the determination of the extinction coefficients of monoclonal antibodies and an Fc-fusion protein under native as well as under denaturing conditions. An intra-assay precision of 0.9% and an accuracy of 1.8% compared to the theoretical value was achieved for monoclonal antibodies. Due to the large number of data points of a single dataset, no meaningful difference between the ProteomeLab XL-I and the new Optima AUC platform could be observed. 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dn/dc
values taking glycosylation and solvent composition into account allowed the determination of the extinction coefficients of monoclonal antibodies and an Fc-fusion protein under native as well as under denaturing conditions. An intra-assay precision of 0.9% and an accuracy of 1.8% compared to the theoretical value was achieved for monoclonal antibodies. Due to the large number of data points of a single dataset, no meaningful difference between the ProteomeLab XL-I and the new Optima AUC platform could be observed. Thus, the AUC-based approach offers a precise, convenient and versatile alternative to conventional methods like total amino acid analysis (AAA).</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>29666888</pmid><doi>10.1007/s00249-018-1299-x</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-9392-0700</orcidid></addata></record> |
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subjects | Amino acid sequence Amino acids Biochemistry Biological and Medical Physics Biomedical and Life Sciences Biopharmaceuticals Biophysics Cell Biology Coefficients Data points Fc receptors Fusion protein Glycosylation Life Sciences Membrane Biology Monoclonal antibodies Nanotechnology Neurobiology Optics Original Article Photometry Proteins |
title | Precise determination of protein extinction coefficients under native and denaturing conditions using SV-AUC |
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