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免疫遗传学分析揭示人类 V 区中非典型半胱氨酸景观。

Landscape of Non-canonical Cysteines in Human V Repertoire Revealed by Immunogenetic Analysis.

机构信息

Biologics Research, Sanofi, Framingham, MA 01701, USA.

出版信息

Cell Rep. 2020 Jun 30;31(13):107831. doi: 10.1016/j.celrep.2020.107831.

Abstract

Human antibody repertoire data captured through next-generation sequencing (NGS) has enabled deeper insights into B cell immunogenetics and paratope diversity. By analyzing large public NGS datasets, we map the landscape of non-canonical cysteines in human variable heavy-chain domains (Vs) at the repertoire level. We identify remarkable usage of non-canonical cysteines within the heavy-chain complementarity-determining region 3 (CDR-H3) and other CDRs and framework regions. Furthermore, our study reveals the diversity and location of non-canonical cysteines and their associated motifs in human Vs, which are reminiscent of and more complex than those found in other non-human species such as chicken, camel, llama, shark, and cow. These results explain how non-canonical cysteines strategically occur in the human antibodyome to expand its paratope space. This study will guide the design of human antibodies harboring disulfide-stabilized long CDR-H3s to access difficult-to-target epitopes and influence a paradigm shift in developability involving non-canonical cysteines.

摘要

通过下一代测序 (NGS) 捕获的人类抗体库数据使我们能够更深入地了解 B 细胞免疫遗传学和抗原结合部位的多样性。通过分析大型公共 NGS 数据集,我们在抗体库水平上绘制了人类可变重链结构域 (VH) 中非典型半胱氨酸的图谱。我们发现,重链互补决定区 3 (CDR-H3) 和其他 CDR 及框架区中存在大量非典型半胱氨酸的使用。此外,我们的研究揭示了人类 VH 中非典型半胱氨酸及其相关基序的多样性和位置,这些半胱氨酸类似于而非人类物种(如鸡、骆驼、美洲驼、鲨鱼和牛)中发现的半胱氨酸,而且更为复杂。这些结果解释了非典型半胱氨酸如何在人类抗体库中策略性地出现以扩大其抗原结合部位的空间。本研究将指导设计具有二硫键稳定长 CDR-H3 的人类抗体,以靶向难以靶向的表位,并影响涉及非典型半胱氨酸的可开发性范式转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f02/7326410/86f92752099f/fx1_lrg.jpg

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