abYpap:使用梯度增强回归预测抗体V H/V L包装的改进。

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Protein Engineering Design & Selection Pub Date : 2023-01-21 DOI:10.1093/protein/gzad021
Veronica A Boron, Andrew C R Martin
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引用次数: 0

摘要

抗体的Fv区(包括VH和VL结构域)是负责结合靶标的区域,因此抗体具有特异性。这两个结构域相对的取向或包装会影响Fv区的地形,从而影响抗体的结合亲和力。我们提出了一种改进的预测VH和VL畴之间填充角的abYpap方法。有了现在可用的大数据集,与以前的工作相比,我们能够大大扩展可以使用的特征的数量。机器学习模型通过使用37个选定的残基(以前是13个)以及包括最可变的“互补决定区域”(CDR-L1, CDR-L2和CDR-H3)的长度来调整以提高性能。在预测填料角时,我们的方法比以前的版本有了很大的改进,并且也反对其他建模方法。补充信息:补充数据可在蛋白质工程设计与选择在线获取。
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abYpap: improvements to the prediction of antibody VH/VL packing using gradient boosted regression.

The Fv region of the antibody (comprising VH and VL domains) is the area responsible for target binding and thus the antibody's specificity. The orientation, or packing, of these two domains relative to each other influences the topography of the Fv region, and therefore can influence the antibody's binding affinity. We present abYpap, an improved method for predicting the packing angle between the VH and VL domains. With the large data set now available, we were able to expand greatly the number of features that could be used compared with our previous work. The machine-learning model was tuned for improved performance using 37 selected residues (previously 13) and also by including the lengths of the most variable 'complementarity determining regions' (CDR-L1, CDR-L2 and CDR-H3). Our method shows large improvements from the previous version, and also against other modeling approaches, when predicting the packing angle.

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来源期刊
Protein Engineering Design & Selection
Protein Engineering Design & Selection 生物-生化与分子生物学
CiteScore
3.30
自引率
4.20%
发文量
14
审稿时长
6-12 weeks
期刊介绍: Protein Engineering, Design and Selection (PEDS) publishes high-quality research papers and review articles relevant to the engineering, design and selection of proteins for use in biotechnology and therapy, and for understanding the fundamental link between protein sequence, structure, dynamics, function, and evolution.
期刊最新文献
TIMED-Design: flexible and accessible protein sequence design with convolutional neural networks. Correction to: De novo design of a polycarbonate hydrolase. Interactive computational and experimental approaches improve the sensitivity of periplasmic binding protein-based nicotine biosensors for measurements in biofluids. Design of functional intrinsically disordered proteins. The shortest path method (SPM) webserver for computational enzyme design.
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