Suppr超能文献

EASINESS:辅助快速亲和成熟进化系统。

EASINESS: Assisted Speedy affINity-maturation Evolution SyStem.

机构信息

Shanghai Center for Systems Biomedicine, Key Laboratory of Systems Biomedicine (Ministry of Education), Shanghai Jiao Tong University, Shanghai, China.

Engineering Research Center of Cell and Therapeutic Antibody of Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Front Immunol. 2021 Dec 3;12:747267. doi: 10.3389/fimmu.2021.747267. eCollection 2021.

Abstract

Antibodies are one of the most important groups of biomolecules for both clinical and basic research and have been developed as potential therapeutics. Affinity is the key feature for biological activity and clinical efficacy of an antibody, especially of therapeutic antibodies, and thus antibody affinity improvement is indispensable and still remains challenging. To address this issue, we developed the Assisted Speed affINity-maturation Evolution SyStem (EASINESS) for continuous directed evolution of Ag-Ab interactions. Two key components of EASINESS include a mutation system modified from error-prone DNA polymerase I (Pol I) that selectively mutates ColE1 plasmids in and a protein-protein interaction selection system from mDHFR split fragments. We designed a GCN4 variant which barely forms a homodimer, and during a single round of evolution, we reversed the homodimer formation activity from the GCN4 variant to verify the feasibility of EASINESS. We then selected a potential therapeutic antibody 18A4Hu and improved the affinity of the antibody (18A4Hu) to its target (ARG2) 12-fold in 7 days while requiring very limited hands-on time. Remarkably, these variants of 18A4Hu revealed a significant improved ability to inhibit melanoma pulmonary metastasis in a mouse model. These results indicate EASINESS could be as an attractive choice for antibody affinity maturation.

摘要

抗体是临床和基础研究中最重要的生物分子之一,已被开发为潜在的治疗药物。亲和力是抗体(尤其是治疗性抗体)生物活性和临床疗效的关键特征,因此,提高抗体亲和力是必不可少的,而且仍然具有挑战性。为了解决这个问题,我们开发了辅助速度亲和成熟进化系统(EASINESS),用于持续定向进化 Ag-Ab 相互作用。EASINESS 的两个关键组成部分包括一个源自易错 DNA 聚合酶 I(Pol I)的突变系统,该系统选择性地突变 ColE1 质粒和来自 mDHFR 分裂片段的蛋白质-蛋白质相互作用选择系统。我们设计了一个 GCN4 变体,几乎不形成同源二聚体,在一轮进化中,我们将 GCN4 变体的同源二聚体形成活性逆转,以验证 EASINESS 的可行性。然后,我们选择了一种潜在的治疗性抗体 18A4Hu,并在 7 天内将该抗体(18A4Hu)对其靶标(ARG2)的亲和力提高了 12 倍,而所需的人工操作时间非常有限。值得注意的是,这些 18A4Hu 变体在小鼠模型中显示出显著提高抑制黑色素瘤肺转移的能力。这些结果表明,EASINESS 可能成为抗体亲和力成熟的一个有吸引力的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c63e/8677947/3ba4b8efed25/fimmu-12-747267-g001.jpg

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