sars - cov -2阻断重组抗体片段的分离及其与变异刺突蛋白结合的特征

IF 4.1 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
D. Antoine, M. Mohammadi, C. McDermott, Eithne Walsh, P. Johnson, K. Wawrousek, J. Wall
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引用次数: 1

摘要

新冠肺炎是由严重急性呼吸系统疾病引起的冠状病毒2。从2019年首次出现在中国武汉开始,它迅速发展成为一场全球大流行。除了疫苗,治疗性抗体在立即治疗易感个体以减轻疾病严重程度方面发挥着重要作用。在本研究中,利用噬菌体展示技术分离了与严重急性呼吸系统综合征冠状病毒2型武汉-Hu-1刺突蛋白受体结合结构域(RBD)结合的人单链抗体片段。在分离的8种RBD结合单链抗体中,有2种抑制了RBD与VeroE6细胞上ACE2蛋白的相互作用。在拉曼光谱免疫测试中,两种scFv也表现出与严重急性呼吸系统综合征冠状病毒2型德尔塔变异刺突蛋白的结合,但与奥密克戎变异刺突蛋白质没有结合。该研究证明了重组抗体方法快速分离具有病毒中和潜力的抗体部分的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation of SARS-CoV-2-blocking recombinant antibody fragments and characterisation of their binding to variant spike proteins
COVID-19 is a severe acute respiratory disease caused by SARS-CoV-2. From its initial appearance in Wuhan, China in 2019, it developed rapidly into a global pandemic. In addition to vaccines, therapeutic antibodies play an important role in immediately treating susceptible individuals to lessen severity of the disease. In this study, phage display technology was utilised to isolate human scFv antibody fragments that bind the receptor-binding domain (RBD) of SARS-CoV-2 Wuhan-Hu-1 spike protein. Of eight RBD-binding scFvs isolated, two inhibited interaction of RBD with ACE2 protein on VeroE6 cells. Both scFvs also exhibited binding to SARS-CoV-2 Delta variant spike protein but not to Omicron variant spike protein in a Raman spectroscopy immunotest. The study demonstrates the potential of recombinant antibody approaches to rapidly isolate antibody moieties with virus neutralisation potential.
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来源期刊
Frontiers in Nanotechnology
Frontiers in Nanotechnology Engineering-Electrical and Electronic Engineering
CiteScore
7.10
自引率
0.00%
发文量
96
审稿时长
13 weeks
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