• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

腺嘌呤脱氨酶在抗体亲和力成熟中的应用。

The application of adenine deaminase in antibody affinity maturation.

机构信息

Key Laboratory for Protein and Peptide Pharmaceuticals, Institute of Biophysics, National Laboratory of Biomacromolecules, Chinese Academy of Sciences, Beijing, 100101, China.

University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Appl Microbiol Biotechnol. 2023 Apr;107(7-8):2661-2670. doi: 10.1007/s00253-022-12324-z. Epub 2023 Mar 16.

DOI:10.1007/s00253-022-12324-z
PMID:36929186
Abstract

Previously, we established a platform for antibody/protein affinity maturation based on CHO cell display. The gene of interest was mutated by activation-induced cytidine deaminase (AID), and then, a mutation library mainly containing G/C to A/T conversion was obtained by simply proliferating cells. However, the AID-induced G/C to A/T conversion limits the diversity space of the mutation library. In contrast to AID, adenine deaminase (ADA) can convert A/T to G/C. In this study, we demonstrated that ADA could efficiently induce random A/T to G/C mutations on the target gene in the CHO cell display and could be applied in affinity maturation. Our data also showed that more mutant types were obtained through the combined use of AID and ADA, thus offering an opportunity to acquire new mutants offering higher affinities than those obtained by only using AID. Examples presented in this study showed that ADA contributed to the improvement of antibody affinity either with or without AID in CHO display. KEY POINTS: • ADA is able to induce random mutations on antibody gene in mammalian cells. • ADA induces mutations on A/T bases to compensate AID which can induce mutation on G/C. • Combination of AID and ADA can increase mutation types and maturation efficiencies.

摘要

先前,我们建立了一个基于 CHO 细胞展示的抗体/蛋白质亲和力成熟平台。通过激活诱导的胞嘧啶脱氨酶(AID)对感兴趣的基因进行突变,然后通过简单地增殖细胞获得主要包含 G/C 到 A/T 转换的突变文库。然而,AID 诱导的 G/C 到 A/T 转换限制了突变文库的多样性空间。与 AID 相比,腺嘌呤脱氨酶(ADA)可以将 A/T 转换为 G/C。在这项研究中,我们证明了 ADA 可以在 CHO 细胞展示中有效地诱导目标基因上随机的 A/T 到 G/C 突变,并可应用于亲和力成熟。我们的数据还表明,通过同时使用 AID 和 ADA 可以获得更多的突变类型,从而有机会获得比仅使用 AID 获得的更高亲和力的新突变体。本研究中的实例表明,ADA 有助于提高 CHO 展示中抗体的亲和力,无论是单独使用 AID 还是同时使用 AID 和 ADA。

关键点

• ADA 能够在哺乳动物细胞中诱导抗体基因的随机突变。

• ADA 诱导 A/T 碱基的突变,以补偿只能诱导 G/C 突变的 AID。

• AID 和 ADA 的组合可以增加突变类型和成熟效率。

相似文献

1
The application of adenine deaminase in antibody affinity maturation.腺嘌呤脱氨酶在抗体亲和力成熟中的应用。
Appl Microbiol Biotechnol. 2023 Apr;107(7-8):2661-2670. doi: 10.1007/s00253-022-12324-z. Epub 2023 Mar 16.
2
Coupling recombinase-mediated cassette exchange with somatic hypermutation for antibody affinity maturation in CHO cells.在CHO细胞中将重组酶介导的盒式交换与体细胞高频突变相结合以实现抗体亲和力成熟
Biotechnol Bioeng. 2016 Jan;113(1):39-51. doi: 10.1002/bit.25541. Epub 2015 Jul 31.
3
High efficiency CHO cell display-based antibody maturation.基于高效 CHO 细胞展示的抗体成熟。
Sci Rep. 2020 May 15;10(1):8102. doi: 10.1038/s41598-020-65044-7.
4
Activation-Induced Cytidine Deaminase Aided In Vitro Antibody Evolution.活化诱导胞苷脱氨酶辅助的体外抗体进化
Methods Mol Biol. 2018;1707:1-14. doi: 10.1007/978-1-4939-7474-0_1.
5
Simultaneous Maturation of Single Chain Antibody Stability and Affinity by CHO Cell Display.通过CHO细胞展示实现单链抗体稳定性和亲和力的同时成熟
Bioengineering (Basel). 2022 Aug 2;9(8):360. doi: 10.3390/bioengineering9080360.
6
An Efficient Exogenous Gene Insertion Site in CHO Cells with High Transcription Level to Enhance AID-Induced Mutation.CHO 细胞中高效的转录水平外源基因插入位点增强 AID 诱导的突变。
Biotechnol J. 2020 May;15(5):e1900313. doi: 10.1002/biot.201900313. Epub 2020 Feb 6.
7
Fast-tracking antibody maturation using a B cell-based display system.利用基于 B 细胞的展示系统实现抗体的快速成熟。
MAbs. 2022 Jan-Dec;14(1):2122275. doi: 10.1080/19420862.2022.2122275.
8
Enhancers Improve the AID-Induced Hypermutation in Episomal Vector for Antibody Affinity Maturation in Mammalian Cell Display.增强子改善游离型载体中由激活诱导的胞嘧啶脱氨酶引起的超突变,用于哺乳动物细胞展示中的抗体亲和力成熟。
Antibodies (Basel). 2018 Dec 13;7(4):42. doi: 10.3390/antib7040042.
9
In vitro affinity maturation of a natural human antibody overcomes a barrier to in vivo affinity maturation.天然人源抗体的体外亲和力成熟克服了体内亲和力成熟的一个障碍。
MAbs. 2014 Mar-Apr;6(2):437-45. doi: 10.4161/mabs.27875. Epub 2014 Jan 16.
10
A rapid screening and production method using a novel mammalian cell display to isolate human monoclonal antibodies.一种使用新型哺乳动物细胞展示技术快速筛选和生产的方法,用于分离人源单克隆抗体。
Biochem Biophys Res Commun. 2013 Nov 8;441(1):59-64. doi: 10.1016/j.bbrc.2013.10.007. Epub 2013 Oct 16.

本文引用的文献

1
Antibody display technologies: selecting the cream of the crop.抗体展示技术:精选优质产品。
Biol Chem. 2021 Mar 23;403(5-6):455-477. doi: 10.1515/hsz-2020-0377. Print 2022 Apr 26.
2
In vivo diversification of target genomic sites using processive base deaminase fusions blocked by dCas9.利用被 dCas9 阻断的持续性碱基脱氨酶融合物在体内对靶基因组位点进行多样化修饰。
Nat Commun. 2020 Dec 22;11(1):6436. doi: 10.1038/s41467-020-20230-z.
3
Phage-assisted evolution of an adenine base editor with improved Cas domain compatibility and activity.
通过噬菌体辅助进化提高 Cas 结构域兼容性和活性的腺嘌呤碱基编辑器。
Nat Biotechnol. 2020 Jul;38(7):883-891. doi: 10.1038/s41587-020-0453-z. Epub 2020 Mar 16.
4
High efficiency CHO cell display-based antibody maturation.基于高效 CHO 细胞展示的抗体成熟。
Sci Rep. 2020 May 15;10(1):8102. doi: 10.1038/s41598-020-65044-7.
5
Protein engineering approaches for antibody fragments: directed evolution and rational design approaches.抗体片段的蛋白质工程方法:定向进化和理性设计方法。
Turk J Biol. 2019 Feb 7;43(1):1-12. doi: 10.3906/biy-1809-28. eCollection 2019.
6
Precision genome engineering through adenine base editing in plants.通过腺嘌呤碱基编辑在植物中进行精确基因组工程。
Nat Plants. 2018 Jul;4(7):427-431. doi: 10.1038/s41477-018-0178-x. Epub 2018 Jun 4.
7
Improving cytidine and adenine base editors by expression optimization and ancestral reconstruction.通过表达优化和祖先重建提高胞嘧啶和腺嘌呤碱基编辑器的性能。
Nat Biotechnol. 2018 Oct;36(9):843-846. doi: 10.1038/nbt.4172. Epub 2018 May 29.
8
Adenine base editing in mouse embryos and an adult mouse model of Duchenne muscular dystrophy.腺嘌呤碱基编辑在小鼠胚胎和杜氏肌营养不良症的成年小鼠模型中的应用。
Nat Biotechnol. 2018 Jul;36(6):536-539. doi: 10.1038/nbt.4148. Epub 2018 Apr 27.
9
Highly Efficient A·T to G·C Base Editing by Cas9n-Guided tRNA Adenosine Deaminase in Rice.利用Cas9n引导的tRNA腺苷脱氨酶在水稻中实现高效的A·T到G·C碱基编辑
Mol Plant. 2018 Apr 2;11(4):631-634. doi: 10.1016/j.molp.2018.02.008. Epub 2018 Feb 22.
10
Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage.基因组DNA中A•T到G•C的可编程碱基编辑,无需DNA切割。
Nature. 2017 Nov 23;551(7681):464-471. doi: 10.1038/nature24644. Epub 2017 Oct 25.