Computational Design of Potential Binder Protein for SARS-CoV-2 Spike RBD through A Novel Deep Neural Network Based-Protein Outpainting Algorithm

Bingya Duan, Yingfei Sun
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Abstract

COVID-19 caused by SARS-CoV-2 is seriously endangering the health of all human beings. There is an urgent need for drugs that can inhibit the replication and propagation of the virus. Traditional macromolecular drugs have long discovery and development cycles and high experimental costs, which can't give rapid response to new viruses. Through computational protein design method, scientists have designed binder proteins with high affinity for the RBD of SARS-CoV-2 spike protein which can effectively inhibit virus replication. However, traditional computational protein design methods rely heavily on human experience and domain knowledge of protein design, and the protein design workflow is too complicated to be widely accepted and used in academia and industry. Based on previous work in the field of deep neural network protein structure prediction and protein design, we developed a novel protein outpainting method that can generate the remaining part of the protein based on a given hot spot motif and complete the entire protein. This method can generate stable protein scaffold which can support the functional hot spot motif, resulting in a protein with excellent thermal stability and developability. We tested this method in a drug discovery project with the aim of designing new SARS-CoV-2 inhibitors. Several proteins are obtained which are predicted to be stable and may have high affinity for the RBD of the SARS-CoV-2 spike protein. Although they have not been verified by wet-lab experiments, we believe that these proteins have great potential to be developed into effective drugs for the treatment of COVID-19. The protein outpainting algorithm proposed in this paper has great advantages over traditional protein design methods. It can be applied to many fields that require the design of functional proteins, such as protein drug design, enzyme de novo design, vaccine design, etc. The method will play an important role in reducing the cost of experiments, shortening the research and development period, and improving the successful rate of biological research and development.
基于深度神经网络的新型蛋白脱色算法的SARS-CoV-2刺突RBD潜在结合蛋白计算设计
由SARS-CoV-2引发的新冠肺炎疫情严重危害全人类健康。目前迫切需要能够抑制病毒复制和繁殖的药物。传统的大分子药物发现开发周期长,实验成本高,无法对新型病毒做出快速反应。通过计算蛋白设计方法,科学家设计出了与SARS-CoV-2刺突蛋白RBD具有高亲和力的结合蛋白,能够有效抑制病毒复制。然而,传统的计算蛋白质设计方法严重依赖于人类的经验和蛋白质设计的领域知识,蛋白质设计工作流程过于复杂,难以被学术界和工业界广泛接受和使用。在深度神经网络蛋白结构预测和蛋白设计研究的基础上,我们提出了一种基于给定热点基序生成蛋白剩余部分并完成整个蛋白的新方法。该方法可以生成稳定的支持功能热点基序的蛋白质支架,从而获得具有良好热稳定性和可展性的蛋白质。我们在一个药物发现项目中测试了这种方法,目的是设计新的SARS-CoV-2抑制剂。获得了几种预测稳定的蛋白,可能对SARS-CoV-2刺突蛋白的RBD具有高亲和力。虽然尚未通过湿室实验验证,但我们认为这些蛋白质具有开发成治疗COVID-19的有效药物的巨大潜力。与传统的蛋白质设计方法相比,本文提出的蛋白质绘制算法具有很大的优势。它可以应用于许多需要功能蛋白设计的领域,如蛋白质药物设计、酶从头设计、疫苗设计等。该方法将对降低实验成本、缩短研发周期、提高生物研发成功率等方面起到重要作用。
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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