YabXnization platform: A monoclonal antibody heterologization server based on rational design and artificial intelligence-assisted computation

IF 4.4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiaohu Hao, Dongping Liu, Long Fan
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Abstract

The application of antibody therapeutics is promising in the field of immunotherapy. While, heterologization should be done in most cases before applying the therapeutic antibodies into bodies, e.g., humanization, caninization and felinization for human beings, canine and feline, respectively. Here we report YabXnization, the platform which realizes antibody heterologization on the basis of rational design and artificial intelligence (AI)-assisted computation. YabXnization provides two ways for heterologization: traditional CDR-grafting and backmutation-based rational design; and AI-assisted fusion computational design. Taking humanization as example, both of the two ways first find the proper template for heavy and light chains with CDR-grafting followed. For rational design, bioinformatics analysis-based backmutation is then conducted. For AI-assisted computational design, the backmutation and humanness evaluation are implemented through evolutionary computation framework with DeepForest-based humanness evaluation model and the distance to the previously found human template as objective functions. Finally, the top heterologized antibodies can be provided by YabXnization platform. We examined the platform with 18 antibodies to be heterologized, in which 10 for humanization, 6 for caninization and 2 for felinization, respectively. The heterologized antibodies were measured by indirect ELISA and BLI(Octet)/SPR(Biacore) binding affinity measurement methods. Test results show a 90% success rate with the binding affinity loss of heterologized antibodies within an order of magnitude compared to the corresponding chimeric antibodies. It even shows an increase in the binding affinity on some of the heterologized antibodies. The platform can be reached through .
YabXnization 平台:基于合理设计和人工智能辅助计算的单克隆抗体异源化服务器
抗体疗法在免疫疗法领域的应用前景广阔。然而,在大多数情况下,在将治疗性抗体应用于人体之前都需要进行异源化,例如,人、犬和猫分别需要进行人源化、犬源化和猫源化。在此,我们报告了基于合理设计和人工智能(AI)辅助计算实现抗体异源化的平台--YabXnization。YabXnization提供了两种异源化途径:传统的CDR嫁接和基于反突变的理性设计,以及人工智能辅助的融合计算设计。以人源化为例,这两种方法都是先找到合适的重链和轻链模板,然后进行CDR嫁接。在合理设计方面,首先要进行基于生物信息学分析的反向突变。对于人工智能辅助计算设计,则是通过进化计算框架,以基于 DeepForest 的人性化评价模型和与之前找到的人类模板的距离为目标函数,实现反嬗变和人性化评价。最后,YabXnization 平台可以提供顶级异源化抗体。我们使用该平台对 18 种抗体进行了异源化,其中 10 种为人源化,6 种为犬源化,2 种为猫源化。异源化抗体通过间接 ELISA 和 BLI(Octet)/SPR(Biacore)结合亲和力测量方法进行测量。测试结果显示,异源化抗体的成功率为 90%,与相应的嵌合抗体相比,异源化抗体的结合亲和力损失在一个数量级之内。甚至某些异源化抗体的结合亲和力还有所增加。该平台可通过.NET Framework 3.0.0.1访问。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Computational and structural biotechnology journal
Computational and structural biotechnology journal Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
9.30
自引率
3.30%
发文量
540
审稿时长
6 weeks
期刊介绍: Computational and Structural Biotechnology Journal (CSBJ) is an online gold open access journal publishing research articles and reviews after full peer review. All articles are published, without barriers to access, immediately upon acceptance. The journal places a strong emphasis on functional and mechanistic understanding of how molecular components in a biological process work together through the application of computational methods. Structural data may provide such insights, but they are not a pre-requisite for publication in the journal. Specific areas of interest include, but are not limited to: Structure and function of proteins, nucleic acids and other macromolecules Structure and function of multi-component complexes Protein folding, processing and degradation Enzymology Computational and structural studies of plant systems Microbial Informatics Genomics Proteomics Metabolomics Algorithms and Hypothesis in Bioinformatics Mathematical and Theoretical Biology Computational Chemistry and Drug Discovery Microscopy and Molecular Imaging Nanotechnology Systems and Synthetic Biology
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