Improvement of protein binding capacity of acrylic-acid-grafted fibers by polymer root-to-brush shift
A weak acid cation exchange fiber used for large-scale antibody purification was prepared by radiation-induced graft polymerization of acrylic acid (AA) onto a commercially available nylon-6 fiber. The AA-grafted fiber was post-treated by conditioning in NaOH aqueous solution at 298 K followed by im...
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Veröffentlicht in: | Radiation physics and chemistry (Oxford, England : 1993) England : 1993), 2019-05, Vol.158, p.131-136 |
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creator | Matsuzaki, Yuka Itabashi, Takeshi Kawai-Noma, Shigeko Umeno, Daisuke Saito, Kyoichi |
description | A weak acid cation exchange fiber used for large-scale antibody purification was prepared by radiation-induced graft polymerization of acrylic acid (AA) onto a commercially available nylon-6 fiber. The AA-grafted fiber was post-treated by conditioning in NaOH aqueous solution at 298 K followed by immersion in water at 353 K to increase the protein binding capacity of the cation exchange fiber. A 2 g/L lysozyme solution buffered at pH 6.0 flowed through a column charged with a treated or untreated AA-grafted fiber at a space velocity of 20 h−1. The 10% dynamic binding capacity of the column charged with the former fiber of 200 mg/mL-column was 5.9-fold that of the column charged with the latter fiber, and 2.3-fold that (88 mg/mL-column) of a column charged with CM Sepharose™ Fast Flow (GE Healthcare).
•Acrylic-acid-grafted fibers were post-treated by immersion in water at 353 K.•Binding capacities of the fibers for lysozyme were evaluated in a flow-through mode.•Dynamic binding capacity (DBC) of the fiber for lysozyme reached 200 mg/mL-bed.•The DBC of the post-treated fiber was 5.9-fold that of the untreated fiber. |
doi_str_mv | 10.1016/j.radphyschem.2018.12.022 |
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•Acrylic-acid-grafted fibers were post-treated by immersion in water at 353 K.•Binding capacities of the fibers for lysozyme were evaluated in a flow-through mode.•Dynamic binding capacity (DBC) of the fiber for lysozyme reached 200 mg/mL-bed.•The DBC of the post-treated fiber was 5.9-fold that of the untreated fiber.</description><identifier>ISSN: 0969-806X</identifier><identifier>EISSN: 1879-0895</identifier><identifier>DOI: 10.1016/j.radphyschem.2018.12.022</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Acrylic acid ; Acrylic-acid-grafted fiber ; Antibodies ; Aqueous solutions ; Binding ; Cation exchanging ; Cationic polymerization ; Conditioning with alkaline solution ; Grafting ; Immersion in hot water ; Ions ; Lysozyme ; Protein-binding capacity ; Proteins ; Radiation effects ; Radiation-induced graft polymerization ; Sodium hydroxide ; Submerging</subject><ispartof>Radiation physics and chemistry (Oxford, England : 1993), 2019-05, Vol.158, p.131-136</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright Elsevier BV May 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-499aa6dd475050b3c95a061180250b9e93a5d5067750fdde84b35a8890572dff3</citedby><cites>FETCH-LOGICAL-c415t-499aa6dd475050b3c95a061180250b9e93a5d5067750fdde84b35a8890572dff3</cites><orcidid>0000-0001-8107-552X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0969806X18301889$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Matsuzaki, Yuka</creatorcontrib><creatorcontrib>Itabashi, Takeshi</creatorcontrib><creatorcontrib>Kawai-Noma, Shigeko</creatorcontrib><creatorcontrib>Umeno, Daisuke</creatorcontrib><creatorcontrib>Saito, Kyoichi</creatorcontrib><title>Improvement of protein binding capacity of acrylic-acid-grafted fibers by polymer root-to-brush shift</title><title>Radiation physics and chemistry (Oxford, England : 1993)</title><description>A weak acid cation exchange fiber used for large-scale antibody purification was prepared by radiation-induced graft polymerization of acrylic acid (AA) onto a commercially available nylon-6 fiber. The AA-grafted fiber was post-treated by conditioning in NaOH aqueous solution at 298 K followed by immersion in water at 353 K to increase the protein binding capacity of the cation exchange fiber. A 2 g/L lysozyme solution buffered at pH 6.0 flowed through a column charged with a treated or untreated AA-grafted fiber at a space velocity of 20 h−1. The 10% dynamic binding capacity of the column charged with the former fiber of 200 mg/mL-column was 5.9-fold that of the column charged with the latter fiber, and 2.3-fold that (88 mg/mL-column) of a column charged with CM Sepharose™ Fast Flow (GE Healthcare).
•Acrylic-acid-grafted fibers were post-treated by immersion in water at 353 K.•Binding capacities of the fibers for lysozyme were evaluated in a flow-through mode.•Dynamic binding capacity (DBC) of the fiber for lysozyme reached 200 mg/mL-bed.•The DBC of the post-treated fiber was 5.9-fold that of the untreated fiber.</description><subject>Acrylic acid</subject><subject>Acrylic-acid-grafted fiber</subject><subject>Antibodies</subject><subject>Aqueous solutions</subject><subject>Binding</subject><subject>Cation exchanging</subject><subject>Cationic polymerization</subject><subject>Conditioning with alkaline solution</subject><subject>Grafting</subject><subject>Immersion in hot water</subject><subject>Ions</subject><subject>Lysozyme</subject><subject>Protein-binding capacity</subject><subject>Proteins</subject><subject>Radiation effects</subject><subject>Radiation-induced graft polymerization</subject><subject>Sodium hydroxide</subject><subject>Submerging</subject><issn>0969-806X</issn><issn>1879-0895</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqNUE2LHCEQlZBAJpv8B0POdkp77NZjGPKxsJBLFvYmtpY7DtNtR52F_vdxmBxyzKl49T6KeoR85NBx4MPnU5etX49bcUecOwFcdVx0IMQrsuNq1AyUlq_JDvSgmYLh6S15V8oJAEYl-x3B-3nN6QVnXCpNgTZQMS50iouPyzN1drUu1u3KWZe3c3SsLTx7zjZU9DTECXOh00bXdN5mzDSnVFlNbMqXcqTlGEN9T94Eey744e-8I4_fvv46_GAPP7_fH748MLfnsrK91tYO3u9HCRKm3mlpYeBcgWhQo-6t9BKGsfHBe1T7qZdWKQ1yFD6E_o58uuW2N35fsFRzSpe8tJNGCCFFD0qqptI3lcuplIzBrDnONm-Gg7m2ak7mn1bNtVXDhWmtNu_h5sX2xkvEbIqLuDj0MaOrxqf4Hyl_AFDPh7E</recordid><startdate>201905</startdate><enddate>201905</enddate><creator>Matsuzaki, Yuka</creator><creator>Itabashi, Takeshi</creator><creator>Kawai-Noma, Shigeko</creator><creator>Umeno, Daisuke</creator><creator>Saito, Kyoichi</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0001-8107-552X</orcidid></search><sort><creationdate>201905</creationdate><title>Improvement of protein binding capacity of acrylic-acid-grafted fibers by polymer root-to-brush shift</title><author>Matsuzaki, Yuka ; Itabashi, Takeshi ; Kawai-Noma, Shigeko ; Umeno, Daisuke ; Saito, Kyoichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-499aa6dd475050b3c95a061180250b9e93a5d5067750fdde84b35a8890572dff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Acrylic acid</topic><topic>Acrylic-acid-grafted fiber</topic><topic>Antibodies</topic><topic>Aqueous solutions</topic><topic>Binding</topic><topic>Cation exchanging</topic><topic>Cationic polymerization</topic><topic>Conditioning with alkaline solution</topic><topic>Grafting</topic><topic>Immersion in hot water</topic><topic>Ions</topic><topic>Lysozyme</topic><topic>Protein-binding capacity</topic><topic>Proteins</topic><topic>Radiation effects</topic><topic>Radiation-induced graft polymerization</topic><topic>Sodium hydroxide</topic><topic>Submerging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsuzaki, Yuka</creatorcontrib><creatorcontrib>Itabashi, Takeshi</creatorcontrib><creatorcontrib>Kawai-Noma, Shigeko</creatorcontrib><creatorcontrib>Umeno, Daisuke</creatorcontrib><creatorcontrib>Saito, Kyoichi</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Radiation physics and chemistry (Oxford, England : 1993)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsuzaki, Yuka</au><au>Itabashi, Takeshi</au><au>Kawai-Noma, Shigeko</au><au>Umeno, Daisuke</au><au>Saito, Kyoichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improvement of protein binding capacity of acrylic-acid-grafted fibers by polymer root-to-brush shift</atitle><jtitle>Radiation physics and chemistry (Oxford, England : 1993)</jtitle><date>2019-05</date><risdate>2019</risdate><volume>158</volume><spage>131</spage><epage>136</epage><pages>131-136</pages><issn>0969-806X</issn><eissn>1879-0895</eissn><abstract>A weak acid cation exchange fiber used for large-scale antibody purification was prepared by radiation-induced graft polymerization of acrylic acid (AA) onto a commercially available nylon-6 fiber. The AA-grafted fiber was post-treated by conditioning in NaOH aqueous solution at 298 K followed by immersion in water at 353 K to increase the protein binding capacity of the cation exchange fiber. A 2 g/L lysozyme solution buffered at pH 6.0 flowed through a column charged with a treated or untreated AA-grafted fiber at a space velocity of 20 h−1. The 10% dynamic binding capacity of the column charged with the former fiber of 200 mg/mL-column was 5.9-fold that of the column charged with the latter fiber, and 2.3-fold that (88 mg/mL-column) of a column charged with CM Sepharose™ Fast Flow (GE Healthcare).
•Acrylic-acid-grafted fibers were post-treated by immersion in water at 353 K.•Binding capacities of the fibers for lysozyme were evaluated in a flow-through mode.•Dynamic binding capacity (DBC) of the fiber for lysozyme reached 200 mg/mL-bed.•The DBC of the post-treated fiber was 5.9-fold that of the untreated fiber.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.radphyschem.2018.12.022</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-8107-552X</orcidid></addata></record> |
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subjects | Acrylic acid Acrylic-acid-grafted fiber Antibodies Aqueous solutions Binding Cation exchanging Cationic polymerization Conditioning with alkaline solution Grafting Immersion in hot water Ions Lysozyme Protein-binding capacity Proteins Radiation effects Radiation-induced graft polymerization Sodium hydroxide Submerging |
title | Improvement of protein binding capacity of acrylic-acid-grafted fibers by polymer root-to-brush shift |
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