基于DART®和TRIDENTTM平台的多特异性、多价抗体分子

Q2 Immunology and Microbiology
Ling Huang, Kalpana Shah, Bhaswati Barat, Chia-Ying K. Lam, Sergey Gorlatov, Valentina Ciccarone, James Tamura, Paul A. Moore, Gundo Diedrich
{"title":"基于DART®和TRIDENTTM平台的多特异性、多价抗体分子","authors":"Ling Huang, Kalpana Shah, Bhaswati Barat, Chia-Ying K. Lam, Sergey Gorlatov, Valentina Ciccarone, James Tamura, Paul A. Moore, Gundo Diedrich","doi":"10.1002/cpim.95","DOIUrl":null,"url":null,"abstract":"Multispecific antibodies bind two or more different antigens and enable new therapeutic applications that cannot be replicated with conventional monoclonal antibodies, such as bridging different cells or bringing soluble proteins in close proximity. The DART and TRIDENT platforms enable the engineering of such antibodies. A DART molecule combines two independent antigen‐binding sites in a stabilized, diabody‐like structure. A DART molecule can be expressed with or without an Fc domain and thus can be tailored to have a long or short half‐life in vivo and to induce or ablate effector function. Linking two DART units or a DART unit and a Fab domain (the latter structure is called TRIDENT format) via an Fc domain creates a monospecific, bispecific, trispecific, or tetraspecific molecule with up to tetravalent targeting of antigens. This article focuses on the design of DART and TRIDENT molecules that target two or three different antigens. © 2020 by John Wiley & Sons, Inc.","PeriodicalId":10733,"journal":{"name":"Current Protocols in Immunology","volume":"129 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpim.95","citationCount":"7","resultStr":"{\"title\":\"Multispecific, Multivalent Antibody-Based Molecules Engineered on the DART® and TRIDENTTM Platforms\",\"authors\":\"Ling Huang, Kalpana Shah, Bhaswati Barat, Chia-Ying K. Lam, Sergey Gorlatov, Valentina Ciccarone, James Tamura, Paul A. Moore, Gundo Diedrich\",\"doi\":\"10.1002/cpim.95\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Multispecific antibodies bind two or more different antigens and enable new therapeutic applications that cannot be replicated with conventional monoclonal antibodies, such as bridging different cells or bringing soluble proteins in close proximity. The DART and TRIDENT platforms enable the engineering of such antibodies. A DART molecule combines two independent antigen‐binding sites in a stabilized, diabody‐like structure. A DART molecule can be expressed with or without an Fc domain and thus can be tailored to have a long or short half‐life in vivo and to induce or ablate effector function. Linking two DART units or a DART unit and a Fab domain (the latter structure is called TRIDENT format) via an Fc domain creates a monospecific, bispecific, trispecific, or tetraspecific molecule with up to tetravalent targeting of antigens. This article focuses on the design of DART and TRIDENT molecules that target two or three different antigens. © 2020 by John Wiley & Sons, Inc.\",\"PeriodicalId\":10733,\"journal\":{\"name\":\"Current Protocols in Immunology\",\"volume\":\"129 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/cpim.95\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Protocols in Immunology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cpim.95\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Immunology and Microbiology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Immunology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpim.95","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Immunology and Microbiology","Score":null,"Total":0}
引用次数: 7

摘要

多特异性抗体结合两种或两种以上不同的抗原,使传统单克隆抗体无法复制的新的治疗应用成为可能,例如桥接不同的细胞或使可溶性蛋白接近。DART和TRIDENT平台使这类抗体的工程化成为可能。DART分子将两个独立的抗原结合位点结合在一个稳定的类似糖尿病体的结构中。DART分子可以带或不带Fc结构域表达,因此可以根据在体内的半衰期长短进行调整,并诱导或消除效应功能。通过Fc结构域连接两个DART单元或一个DART单元和Fab结构域(后一种结构称为TRIDENT格式),可创建单特异性、双特异性、三特异性或四特异性分子,最多可靶向抗原的四价。本文重点介绍了针对两种或三种不同抗原的DART和TRIDENT分子的设计。©2020 by John Wiley &基本方案1:设计和生成编码DART和TRIDENT分子的表达质粒基本方案2:通过CHO细胞的瞬时转染表达DART和TRIDENT分子基本方案3:从CHO细胞上清液中纯化DART和TRIDENT分子
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multispecific, Multivalent Antibody-Based Molecules Engineered on the DART® and TRIDENTTM Platforms
Multispecific antibodies bind two or more different antigens and enable new therapeutic applications that cannot be replicated with conventional monoclonal antibodies, such as bridging different cells or bringing soluble proteins in close proximity. The DART and TRIDENT platforms enable the engineering of such antibodies. A DART molecule combines two independent antigen‐binding sites in a stabilized, diabody‐like structure. A DART molecule can be expressed with or without an Fc domain and thus can be tailored to have a long or short half‐life in vivo and to induce or ablate effector function. Linking two DART units or a DART unit and a Fab domain (the latter structure is called TRIDENT format) via an Fc domain creates a monospecific, bispecific, trispecific, or tetraspecific molecule with up to tetravalent targeting of antigens. This article focuses on the design of DART and TRIDENT molecules that target two or three different antigens. © 2020 by John Wiley & Sons, Inc.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Current Protocols in Immunology
Current Protocols in Immunology Immunology and Microbiology-Immunology
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信