Two-Dimensional SEC-SEC-UV-MALS-dRI Workflow for Streamlined Analysis and Characterization of Biopharmaceuticals
The emergence of complex biological modalities in the biopharmaceutical industry entails a significant expansion of the current analytical toolbox to address the need to deploy meaningful and reliable assays at an unprecedented pace. Size exclusion chromatography (SEC) is an industry standard techni...
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creator | Barrientos, Rodell C. Singh, Andrew N. Ukaegbu, Ophelia Hemida, Mohamed Wang, Heather Haidar Ahmad, Imad Hu, Hang Dunn, Zachary D. Appiah-Amponsah, Emmanuel Regalado, Erik L. |
description | The emergence of complex biological modalities in the biopharmaceutical industry entails a significant expansion of the current analytical toolbox to address the need to deploy meaningful and reliable assays at an unprecedented pace. Size exclusion chromatography (SEC) is an industry standard technique for protein separation and analysis. Some constraints of traditional SEC stem from its restricted ability to resolve complex mixtures and notoriously long run times while also requiring multiple offline separation conditions on different pore size columns to cover a wider molecular size distribution. Two-dimensional liquid chromatography (2D-LC) is becoming an important tool not only to increase peak capacity but also to tune selectivity in a single online method. Herein, an online 2D-LC framework in which both dimensions utilize SEC columns with different pore sizes is introduced with a goal to increase throughput for biomolecule separation and characterization. In addition to improving the separation of closely related species, this online 2D SEC-SEC approach also facilitated the rapid analysis of protein-based mixtures of a wide molecular size range in a single online experimental run bypassing time-consuming deployment of different offline SEC methods. By coupling the second dimension with multiangle light scattering (MALS) and differential refractive index (dRI) detectors, absolute molecular weights of the separated species were obtained without the use of calibration curves. As illustrated in this report for protein mixtures and vaccine processes, this workflow can be used in scenarios where rapid development and deployment of SEC assays are warranted, enabling bioprocess monitoring, purity assessment, and characterization. |
doi_str_mv | 10.1021/acs.analchem.3c05969 |
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Size exclusion chromatography (SEC) is an industry standard technique for protein separation and analysis. Some constraints of traditional SEC stem from its restricted ability to resolve complex mixtures and notoriously long run times while also requiring multiple offline separation conditions on different pore size columns to cover a wider molecular size distribution. Two-dimensional liquid chromatography (2D-LC) is becoming an important tool not only to increase peak capacity but also to tune selectivity in a single online method. Herein, an online 2D-LC framework in which both dimensions utilize SEC columns with different pore sizes is introduced with a goal to increase throughput for biomolecule separation and characterization. In addition to improving the separation of closely related species, this online 2D SEC-SEC approach also facilitated the rapid analysis of protein-based mixtures of a wide molecular size range in a single online experimental run bypassing time-consuming deployment of different offline SEC methods. By coupling the second dimension with multiangle light scattering (MALS) and differential refractive index (dRI) detectors, absolute molecular weights of the separated species were obtained without the use of calibration curves. As illustrated in this report for protein mixtures and vaccine processes, this workflow can be used in scenarios where rapid development and deployment of SEC assays are warranted, enabling bioprocess monitoring, purity assessment, and characterization.</description><identifier>ISSN: 0003-2700</identifier><identifier>ISSN: 1520-6882</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/acs.analchem.3c05969</identifier><identifier>PMID: 38436624</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>analytical chemistry ; Biological Products ; Biomolecules ; biopharmaceutical industry ; Biopharmaceuticals ; bioprocessing ; Chromatography ; Chromatography, Gel ; gel chromatography ; Light scattering ; Liquid chromatography ; Mixtures ; molecular weight ; Pore size ; porosity ; Protein purification ; Proteins ; Proteins - analysis ; rapid methods ; refractive index ; Refractivity ; Refractometry ; Separation ; Size distribution ; Size exclusion chromatography ; Two dimensional analysis ; Vaccines ; Workflow</subject><ispartof>Analytical chemistry (Washington), 2024-03, Vol.96 (12), p.4960-4968</ispartof><rights>2024 Merck & Co., Inc., Rahway, NJ, USA and its affiliates. 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Herein, an online 2D-LC framework in which both dimensions utilize SEC columns with different pore sizes is introduced with a goal to increase throughput for biomolecule separation and characterization. In addition to improving the separation of closely related species, this online 2D SEC-SEC approach also facilitated the rapid analysis of protein-based mixtures of a wide molecular size range in a single online experimental run bypassing time-consuming deployment of different offline SEC methods. By coupling the second dimension with multiangle light scattering (MALS) and differential refractive index (dRI) detectors, absolute molecular weights of the separated species were obtained without the use of calibration curves. As illustrated in this report for protein mixtures and vaccine processes, this workflow can be used in scenarios where rapid development and deployment of SEC assays are warranted, enabling bioprocess monitoring, purity assessment, and characterization.</description><subject>analytical chemistry</subject><subject>Biological Products</subject><subject>Biomolecules</subject><subject>biopharmaceutical industry</subject><subject>Biopharmaceuticals</subject><subject>bioprocessing</subject><subject>Chromatography</subject><subject>Chromatography, Gel</subject><subject>gel chromatography</subject><subject>Light scattering</subject><subject>Liquid chromatography</subject><subject>Mixtures</subject><subject>molecular weight</subject><subject>Pore size</subject><subject>porosity</subject><subject>Protein purification</subject><subject>Proteins</subject><subject>Proteins - analysis</subject><subject>rapid methods</subject><subject>refractive index</subject><subject>Refractivity</subject><subject>Refractometry</subject><subject>Separation</subject><subject>Size distribution</subject><subject>Size exclusion chromatography</subject><subject>Two dimensional analysis</subject><subject>Vaccines</subject><subject>Workflow</subject><issn>0003-2700</issn><issn>1520-6882</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EotvCP0DIEhcuXsYfcZzjshSotAiJbeEYOc5EdUnirZ2oKr--Xu22Bw5wsEaynvcZaV5C3nBYchD8g3VpaUfbu2scltJBUenqGVnwQgDTxojnZAEAkokS4IScpnQDwDlw_ZKcSKOk1kItyO7yLrBPfsAx-ZBtdHu-Zvt39ZN9W222rP1xQX-F-Lvrwx3tQqTbKaIdej9iS1c5cZ98onZs6fraRusmjP6PnbKMho5-9GGXvwfrcJ68s316RV50eeDr4zwjV5_PL9df2eb7l4v1asOsgmpiBWipXGsQDZRdU1RONqbkArAVDoXQ1irUha6c0BqaljelFZVFcE45DSjPyPuDdxfD7YxpqgefHPa9HTHMqZagQAlhlPkvKipZSml0JTP67i_0JswxX2EvlFzqUhVlptSBcjGkFLGrd9EPNt7XHOp9eXUur34srz6Wl2Nvj_K5GbB9Cj22lQE4APv40-J_Oh8A3feoEg</recordid><startdate>20240326</startdate><enddate>20240326</enddate><creator>Barrientos, Rodell C.</creator><creator>Singh, Andrew N.</creator><creator>Ukaegbu, Ophelia</creator><creator>Hemida, Mohamed</creator><creator>Wang, Heather</creator><creator>Haidar Ahmad, Imad</creator><creator>Hu, Hang</creator><creator>Dunn, Zachary D.</creator><creator>Appiah-Amponsah, Emmanuel</creator><creator>Regalado, Erik L.</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-7352-6391</orcidid><orcidid>https://orcid.org/0000-0002-6006-5047</orcidid><orcidid>https://orcid.org/0009-0003-4723-1527</orcidid><orcidid>https://orcid.org/0000-0002-3075-049X</orcidid><orcidid>https://orcid.org/0000-0002-8590-9787</orcidid></search><sort><creationdate>20240326</creationdate><title>Two-Dimensional SEC-SEC-UV-MALS-dRI Workflow for Streamlined Analysis and Characterization of Biopharmaceuticals</title><author>Barrientos, Rodell C. ; 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Chem</addtitle><date>2024-03-26</date><risdate>2024</risdate><volume>96</volume><issue>12</issue><spage>4960</spage><epage>4968</epage><pages>4960-4968</pages><issn>0003-2700</issn><issn>1520-6882</issn><eissn>1520-6882</eissn><abstract>The emergence of complex biological modalities in the biopharmaceutical industry entails a significant expansion of the current analytical toolbox to address the need to deploy meaningful and reliable assays at an unprecedented pace. Size exclusion chromatography (SEC) is an industry standard technique for protein separation and analysis. Some constraints of traditional SEC stem from its restricted ability to resolve complex mixtures and notoriously long run times while also requiring multiple offline separation conditions on different pore size columns to cover a wider molecular size distribution. Two-dimensional liquid chromatography (2D-LC) is becoming an important tool not only to increase peak capacity but also to tune selectivity in a single online method. Herein, an online 2D-LC framework in which both dimensions utilize SEC columns with different pore sizes is introduced with a goal to increase throughput for biomolecule separation and characterization. In addition to improving the separation of closely related species, this online 2D SEC-SEC approach also facilitated the rapid analysis of protein-based mixtures of a wide molecular size range in a single online experimental run bypassing time-consuming deployment of different offline SEC methods. By coupling the second dimension with multiangle light scattering (MALS) and differential refractive index (dRI) detectors, absolute molecular weights of the separated species were obtained without the use of calibration curves. As illustrated in this report for protein mixtures and vaccine processes, this workflow can be used in scenarios where rapid development and deployment of SEC assays are warranted, enabling bioprocess monitoring, purity assessment, and characterization.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>38436624</pmid><doi>10.1021/acs.analchem.3c05969</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7352-6391</orcidid><orcidid>https://orcid.org/0000-0002-6006-5047</orcidid><orcidid>https://orcid.org/0009-0003-4723-1527</orcidid><orcidid>https://orcid.org/0000-0002-3075-049X</orcidid><orcidid>https://orcid.org/0000-0002-8590-9787</orcidid></addata></record> |
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subjects | analytical chemistry Biological Products Biomolecules biopharmaceutical industry Biopharmaceuticals bioprocessing Chromatography Chromatography, Gel gel chromatography Light scattering Liquid chromatography Mixtures molecular weight Pore size porosity Protein purification Proteins Proteins - analysis rapid methods refractive index Refractivity Refractometry Separation Size distribution Size exclusion chromatography Two dimensional analysis Vaccines Workflow |
title | Two-Dimensional SEC-SEC-UV-MALS-dRI Workflow for Streamlined Analysis and Characterization of Biopharmaceuticals |
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