Suppr超能文献

羊驼体内不同类型的单域重链抗体

Distinct types of VHHs in Alpaca.

作者信息

Wang Xinhao, Zhang Lu, Zhang Yao, Li Jiaguo, Xu Wenfeng, Zhu Weimin

机构信息

Drug Discovery and Development, Chantibody Therapeutics, Menlo Park, CA, United States.

Drug Discovery and Development, Shanghai Cell Therapy Group Co. Ltd, Shanghai, China.

出版信息

Front Immunol. 2024 Nov 12;15:1447212. doi: 10.3389/fimmu.2024.1447212. eCollection 2024.

Abstract

INTRODUCTION

VHHs (VH of heavy-chain-only antibodies) represent a unique alternative to Q7 conventional antibodies because of their smaller size, comparable binding affinity and biophysical properties.

METHOD

In this study, we systematically analyzed VHH NGS sequences from 22 Alpacas and structure data from public database.

RESULTS

VHHs in Alpaca can be grouped into five main types with multiple distinct sequence and structure features. Based on the existence of hallmark residues in FR2 region, VHHs can be classified into two groups: nonclassical VHHs (without hallmark residues) and classical VHHs (with hallmark residues). Based on VHH hallmark residues at 42 position (IMGT numbering, FR2 region) and number of cysteines, we found that Alpaca classical VHHs can be further separated into three main types: F_C2 VHHs with F (phenylalanine) at position 42 and having 2 cysteines within sequences, Y_C2 VHHs with Y (tyrosine) at position 42 and having 2 cysteines, and F_C4 with F at position 42 and having 4 cysteines. Non-classical VHHs can be further separated into 2 types based on germlines mapped: N_V3 for VHHs mapped to V3 germlines and N_V4 for V4 germlines. Based on whether FR2 residues are involved in binding, two kinds of paratopes can be identified. Different types of VHHs showed distinct associations with these two paratopes and displayed significant differences in paratope size, residue usage and other structure features.

DISCUSSION

Such results will have significant implications in VHH discovery, engine e ring, and design for innovative therapeutics.

摘要

引言

仅重链抗体的可变区(VHHs)由于其较小的尺寸、相当的结合亲和力和生物物理特性,是传统抗体的一种独特替代品。

方法

在本研究中,我们系统分析了来自22只羊驼的VHHs二代测序序列以及来自公共数据库的结构数据。

结果

羊驼体内的VHHs可分为五种主要类型,具有多种不同的序列和结构特征。根据框架区2(FR2)中标志性残基的存在情况,VHHs可分为两组:非经典VHHs(无标志性残基)和经典VHHs(有标志性残基)。基于第42位(国际免疫学会联合会编号,FR2区)的VHH标志性残基和半胱氨酸数量,我们发现羊驼经典VHHs可进一步分为三种主要类型:第42位为苯丙氨酸(F)且序列中有2个半胱氨酸的F_C2 VHHs,第42位为酪氨酸(Y)且有2个半胱氨酸的Y_C2 VHHs,以及第42位为F且有4个半胱氨酸的F_C4。非经典VHHs根据映射的种系可进一步分为2种类型:映射到V3种系的VHHs为N_V3,映射到V4种系的为N_V4。根据FR2残基是否参与结合,可以识别出两种抗原结合部位。不同类型的VHHs与这两种抗原结合部位表现出不同的关联,并且在抗原结合部位大小、残基使用和其他结构特征方面存在显著差异。

讨论

这些结果将对VHHs的发现、工程改造和创新疗法设计具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f7e/11588638/8d5e98d0b069/fimmu-15-1447212-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