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一个供体即可产生一个高度功能化的体外抗体文库。

A single donor is sufficient to produce a highly functional in vitro antibody library.

机构信息

Specifica Inc, Santa Fe, NM, USA.

New Mexico Consortium, Los Alamos, NM, USA.

出版信息

Commun Biol. 2021 Mar 19;4(1):350. doi: 10.1038/s42003-021-01881-0.

Abstract

Antibody complementarity determining region diversity has been considered to be the most important metric for the production of a functional antibody library. Generally, the greater the antibody library diversity, the greater the probability of selecting a diverse array of high affinity leads. According to this paradigm, the primary means of elevating library diversity has been by increasing the number of donors. In the present study we explored the possibility of creating an in vitro antibody library from a single healthy individual, showing that the number of lymphocytes, rather than the number of donors, is the key criterion in the production of a diverse and functional antibody library. We describe the construction of a high-quality phage display library comprising 5 × 10 human antibodies by applying an efficient B cell extraction protocol from a single donor and a targeted V-gene amplification strategy favoring specific antibody families for their improved developability profiles. Each step of the library generation process was followed and validated by next generation sequencing to monitor the library quality and diversity. The functionality of the library was tested using several therapeutically relevant targets for which a vast number of different antibodies with desired biophysical properties were obtained.

摘要

抗体互补决定区多样性被认为是产生功能性抗体文库的最重要指标。通常,抗体文库的多样性越大,选择多样化高亲和力先导的可能性就越大。根据这一范例,提高文库多样性的主要手段一直是增加供体的数量。在本研究中,我们探索了从单个健康个体中创建体外抗体文库的可能性,结果表明,产生多样化和功能齐全的抗体文库的关键标准是淋巴细胞的数量,而不是供体的数量。我们描述了一种通过从单个供体应用高效 B 细胞提取方案和靶向 V 基因扩增策略来构建包含 5×10 个人抗体的高质量噬菌体展示文库的方法,该策略有利于特定的抗体家族,以提高其可开发性。通过下一代测序来监测文库质量和多样性,对文库生成过程的每个步骤进行了跟踪和验证。通过使用多个治疗相关靶点来测试文库的功能,这些靶点获得了大量具有所需生物物理特性的不同抗体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b8/7979914/6dd1837e9a6d/42003_2021_1881_Fig1_HTML.jpg

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