基于GB1结构域的SARS-CoV-2刺突糖蛋白模拟抗体设计:分子模拟与实验研究

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anderson A. E Santo, Aline Reis, Anderson A. Pinheiro, Paulo I. da Costa* and Gustavo T. Feliciano*, 
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引用次数: 0

摘要

在快速而重大的技术变革背景下,创新的人工智能(AI)方法自然而然地出现在生物活性分子的设计中。在这项研究中,我们证明了模拟抗体(MA)的设计可以使用传统分子模拟中使用的软件和算法的组合来实现。这种组合,组织为遗传算法(GA),有可能解决生物活性分子设计中的主要挑战之一:遗传算法收敛迅速发生,由于基于抗原表面分子间相互作用的初始种群的仔细选择。实验免疫酶测试证明,GA成功地优化了其中一种MA的分子识别能力。本研究的一个重要成果是发现了新的结构基序,这些基序可以基于MA结构本身以新颖和创新的方式设计,从而消除了对已有数据库的需求。通过本研究开发的GA,我们展示了一种能够指导新生物活性分子开发实验方法的新方案的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design of Mimetic Antibodies Targeting the SARS-CoV-2 Spike Glycoprotein Based on the GB1 Domain: A Molecular Simulation and Experimental Study

In the context of fast and significant technological transformations, it is natural for innovative artificial intelligence (AI) methods to emerge for the design of bioactive molecules. In this study, we demonstrated that the design of mimetic antibodies (MA) can be achieved using a combination of software and algorithms traditionally employed in molecular simulation. This combination, organized as a genetic algorithm (GA), has the potential to address one of the main challenges in the design of bioactive molecules: GA convergence occurs rapidly due to the careful selection of initial populations based on intermolecular interactions at antigenic surfaces. Experimental immunoenzymatic tests prove that the GA successfully optimized the molecular recognition capacity of one of the MA. One of the significant results of this study is the discovery of new structural motifs, which can be designed in an original and innovative way based on the MA structure itself, eliminating the need for preexisting databases. Through the GA developed in this study, we demonstrated the application of a new protocol capable of guiding experimental methods in the development of new bioactive molecules.

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来源期刊
Biochemistry Biochemistry
Biochemistry Biochemistry 生物-生化与分子生物学
CiteScore
5.50
自引率
3.40%
发文量
336
审稿时长
1-2 weeks
期刊介绍: Biochemistry provides an international forum for publishing exceptional, rigorous, high-impact research across all of biological chemistry. This broad scope includes studies on the chemical, physical, mechanistic, and/or structural basis of biological or cell function, and encompasses the fields of chemical biology, synthetic biology, disease biology, cell biology, nucleic acid biology, neuroscience, structural biology, and biophysics. In addition to traditional Research Articles, Biochemistry also publishes Communications, Viewpoints, and Perspectives, as well as From the Bench articles that report new methods of particular interest to the biological chemistry community.
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