抗体
优先次序
计算机科学
互补决定区
计算生物学
互补性(分子生物学)
鉴定(生物学)
序列(生物学)
电荷(物理)
化学
食品药品监督管理局
表面电荷
蛋白质工程
组合化学
蛋白质测序
人工智能
生化工程
生物系统
支持向量机
表征(材料科学)
利用
生物信息学
算法
氨基酸
肽序列
双特异性抗体
机器学习
模式识别(心理学)
作者
Wenyang Zou,Jianjun Deng,Yun Shen,Tao Zhang,Zhitong Bing,Lingyan Yuan,Chen Huang,Jianghai Liu,Xuzeng Li
摘要
The developability of antibodies is a critical concern in antibody discovery, encompassing issues such as self-interaction, aggregation, and thermal stability. The use of computational and structure-based tools has greatly improved the evaluation and prioritization of initial antibody sequences. With the increasing demand for subcutaneous administration of small-volume, high-concentration antibody formulations, there is a need for more accurate prediction tools based on protein structures. Our study introduces AB-Panda, a tool based on AlphaFold2-predicted antibody structures and three innovative structure-related metrics. AB-Panda utilizes unit-area hydrophobic value (UHV), unit-area positive charge (UPC), and unit-area negative charge (UNC) to automatically identify hydrophobic and charged patches within the complementarity determining regions (CDRs) of antibodies. Through the analysis of the 919 clinical stage therapeutic (CST) antibodies, we have established recommended ranges of UHV, UPC, and UNC as reference standards for antibody developability. AB-Panda offers clear visualizations of surface hydrophobic and charge distribution, facilitating the identification of problematic amino acids and providing suggestions for further sequence engineering. Additionally, AB-Panda has been integrated into a web application, available at https://www.antibodydev.com, by combining UHV, UPC, UNC, and other established computational metrics for the early screening and optimization of antibody sequences.
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