Production of bispecific antibodies in "knobs-into-holes" using a cell-free expression system
Bispecific antibodies have emerged in recent years as a promising field of research for therapies in oncology, inflammable diseases, and infectious diseases. Their capability of dual target recognition allows for novel therapeutic hypothesis to be tested, where traditional mono-specific antibodies w...
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Veröffentlicht in: | mAbs 2015-01, Vol.7 (1), p.231-242 |
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creator | Xu, Yiren Lee, John Tran, Cuong Heibeck, Tyler H Wang, Willie D Yang, Junhao Stafford, Ryan L Steiner, Alexander R Sato, Aaron K Hallam, Trevor J Yin, Gang |
description | Bispecific antibodies have emerged in recent years as a promising field of research for therapies in oncology, inflammable diseases, and infectious diseases. Their capability of dual target recognition allows for novel therapeutic hypothesis to be tested, where traditional mono-specific antibodies would lack the needed mode of target engagement. Among extremely diverse architectures of bispecific antibodies, knobs-into-holes (KIHs) technology, which involves engineering CH3 domains to create either a "knob" or a "hole" in each heavy chain to promote heterodimerization, has been widely applied. Here, we describe the use of a cell-free expression system (Xpress CF) to produce KIH bispecific antibodies in multiple scaffolds, including 2-armed heterodimeric scFv-KIH and one-armed asymmetric BiTE-KIH with tandem scFv. Efficient KIH production can be achieved by manipulating the plasmid ratio between knob and hole, and further improved by addition of prefabricated knob or hole. These studies demonstrate the versatility of Xpress CF in KIH production and provide valuable insights into KIH construct design for better assembly and expression titer. |
doi_str_mv | 10.4161/19420862.2015.989013 |
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Their capability of dual target recognition allows for novel therapeutic hypothesis to be tested, where traditional mono-specific antibodies would lack the needed mode of target engagement. Among extremely diverse architectures of bispecific antibodies, knobs-into-holes (KIHs) technology, which involves engineering CH3 domains to create either a "knob" or a "hole" in each heavy chain to promote heterodimerization, has been widely applied. Here, we describe the use of a cell-free expression system (Xpress CF) to produce KIH bispecific antibodies in multiple scaffolds, including 2-armed heterodimeric scFv-KIH and one-armed asymmetric BiTE-KIH with tandem scFv. Efficient KIH production can be achieved by manipulating the plasmid ratio between knob and hole, and further improved by addition of prefabricated knob or hole. These studies demonstrate the versatility of Xpress CF in KIH production and provide valuable insights into KIH construct design for better assembly and expression titer.</description><identifier>ISSN: 1942-0862</identifier><identifier>EISSN: 1942-0870</identifier><identifier>DOI: 10.4161/19420862.2015.989013</identifier><identifier>PMID: 25427258</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Animals ; Antibodies, Bispecific - biosynthesis ; Antibodies, Bispecific - genetics ; Cell-Free System - metabolism ; CHO Cells ; Cricetinae ; Cricetulus ; Gene Expression ; Humans ; Recombinant Proteins - biosynthesis ; Recombinant Proteins - genetics ; Single-Chain Antibodies - biosynthesis ; Single-Chain Antibodies - genetics</subject><ispartof>mAbs, 2015-01, Vol.7 (1), p.231-242</ispartof><rights>2015 The Author(s). Published with license by Taylor & Francis Group, LLC © Yiren Xu, John Lee, Cuong Tran, Tyler H Heibeck, Willie D Wang, Junhao Yang, Ryan L Stafford, Alexander R Steiner, Aaron K Sato, Trevor J Hallam, and Gang Yin 2015 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-1b2c3c88e82ce2721a227168e25486b54484badf9adf83929cd6e25edd47a5b33</citedby><cites>FETCH-LOGICAL-c408t-1b2c3c88e82ce2721a227168e25486b54484badf9adf83929cd6e25edd47a5b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623329/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623329/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25427258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xu, Yiren</creatorcontrib><creatorcontrib>Lee, John</creatorcontrib><creatorcontrib>Tran, Cuong</creatorcontrib><creatorcontrib>Heibeck, Tyler H</creatorcontrib><creatorcontrib>Wang, Willie D</creatorcontrib><creatorcontrib>Yang, Junhao</creatorcontrib><creatorcontrib>Stafford, Ryan L</creatorcontrib><creatorcontrib>Steiner, Alexander R</creatorcontrib><creatorcontrib>Sato, Aaron K</creatorcontrib><creatorcontrib>Hallam, Trevor J</creatorcontrib><creatorcontrib>Yin, Gang</creatorcontrib><title>Production of bispecific antibodies in "knobs-into-holes" using a cell-free expression system</title><title>mAbs</title><addtitle>MAbs</addtitle><description>Bispecific antibodies have emerged in recent years as a promising field of research for therapies in oncology, inflammable diseases, and infectious diseases. 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These studies demonstrate the versatility of Xpress CF in KIH production and provide valuable insights into KIH construct design for better assembly and expression titer.</description><subject>Animals</subject><subject>Antibodies, Bispecific - biosynthesis</subject><subject>Antibodies, Bispecific - genetics</subject><subject>Cell-Free System - metabolism</subject><subject>CHO Cells</subject><subject>Cricetinae</subject><subject>Cricetulus</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Recombinant Proteins - genetics</subject><subject>Single-Chain Antibodies - biosynthesis</subject><subject>Single-Chain Antibodies - genetics</subject><issn>1942-0862</issn><issn>1942-0870</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkdtKxDAQhoMoKqtvIBK88qZrTm3TG0HEEwh6oZcS0nSq0W6yZlrRt7dlddFAyDCHf_7wEXLA2Vzxgp_wSgmmCzEXjOfzSleMyw2yO6Uzpku2uY4LsUP2EV_ZdErGS7ZNdkSuRClyvUue7lNsBtf7GGhsae1xCc633lEbel_HxgNSH-jRW4g1Zj70MXuJHeARHdCHZ2qpg67L2gRA4XOZAHHSwi_sYbFHtlrbIez_vDPyeHnxcH6d3d5d3Zyf3WZOMd1nvBZOOq1BCwejMW6FKHmhYfSpizpXSqvaNm01Xi0rUbmmGGvQNKq0eS3ljJyudJdDvYDGQeiT7cwy-YVNXyZab_5Xgn8xz_HDqEJIKapR4PhHIMX3AbA3C4_Tx2yAOKDhRS5kWQnNx1a1anUpIiZo12s4MxMc8wvHTHDMCs44dvjX4nroF4X8Bksxi6U</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Xu, Yiren</creator><creator>Lee, John</creator><creator>Tran, Cuong</creator><creator>Heibeck, Tyler H</creator><creator>Wang, Willie D</creator><creator>Yang, Junhao</creator><creator>Stafford, Ryan L</creator><creator>Steiner, Alexander R</creator><creator>Sato, Aaron K</creator><creator>Hallam, Trevor J</creator><creator>Yin, Gang</creator><general>Taylor & Francis</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150101</creationdate><title>Production of bispecific antibodies in "knobs-into-holes" using a cell-free expression system</title><author>Xu, Yiren ; 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Their capability of dual target recognition allows for novel therapeutic hypothesis to be tested, where traditional mono-specific antibodies would lack the needed mode of target engagement. Among extremely diverse architectures of bispecific antibodies, knobs-into-holes (KIHs) technology, which involves engineering CH3 domains to create either a "knob" or a "hole" in each heavy chain to promote heterodimerization, has been widely applied. Here, we describe the use of a cell-free expression system (Xpress CF) to produce KIH bispecific antibodies in multiple scaffolds, including 2-armed heterodimeric scFv-KIH and one-armed asymmetric BiTE-KIH with tandem scFv. Efficient KIH production can be achieved by manipulating the plasmid ratio between knob and hole, and further improved by addition of prefabricated knob or hole. These studies demonstrate the versatility of Xpress CF in KIH production and provide valuable insights into KIH construct design for better assembly and expression titer.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>25427258</pmid><doi>10.4161/19420862.2015.989013</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies, Bispecific - biosynthesis Antibodies, Bispecific - genetics Cell-Free System - metabolism CHO Cells Cricetinae Cricetulus Gene Expression Humans Recombinant Proteins - biosynthesis Recombinant Proteins - genetics Single-Chain Antibodies - biosynthesis Single-Chain Antibodies - genetics |
title | Production of bispecific antibodies in "knobs-into-holes" using a cell-free expression system |
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