Scottish Biologics Facility, Institute of Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZP, UK.
Aberdeen Fungal Group, Institute of Medical Sciences, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK.
Viruses. 2021 Nov 2;13(11):2201. doi: 10.3390/v13112201.
ORF3a has been identified as a viroporin of SARS-CoV-2 and is known to be involved in various pathophysiological activities including disturbance of cellular calcium homeostasis, inflammasome activation, apoptosis induction and disruption of autophagy. ORF3a-targeting antibodies may specifically and favorably modulate these viroporin-dependent pathological activities. However, suitable viroporin-targeting antibodies are difficult to generate because of the well-recognized technical challenge associated with isolating antibodies to complex transmembrane proteins. Here we exploited a naïve human single chain antibody phage display library, to isolate binders against carefully chosen ORF3a recombinant epitopes located towards the extracellular N terminal and cytosolic C terminal domains of the protein using peptide antigens. These binders were subjected to further characterization using enzyme-linked immunosorbent assays and surface plasmon resonance analysis to assess their binding affinities to the target epitopes. Binding to full-length ORF3a protein was evaluated by western blot and fluorescent microscopy using ORF3a transfected cells and SARS-CoV-2 infected cells. Co-localization analysis was also performed to evaluate the "pairing potential" of the selected binders as possible alternative diagnostic or prognostic biomarkers for COVID-19 infections. Both ORF3a N and C termini, epitope-specific monoclonal antibodies were identified in our study. Whilst the linear nature of peptides might not always represent their native conformations in the context of full protein, with carefully designed selection protocols, we have been successful in isolating anti-ORF3a binders capable of recognising regions of the transmembrane protein that are exposed either on the "inside" or "outside" of the infected cell. Their therapeutic potential will be discussed.
ORF3a 已被鉴定为 SARS-CoV-2 的病毒孔蛋白,已知参与多种病理生理活动,包括破坏细胞内钙稳态、炎症小体激活、凋亡诱导和自噬破坏。针对 ORF3a 的靶向抗体可能会特异性地、有利地调节这些病毒孔蛋白依赖性的病理生理活动。然而,由于与分离复杂跨膜蛋白的抗体相关的公认技术挑战,合适的病毒孔蛋白靶向抗体很难产生。在这里,我们利用一个原始的人源单链抗体噬菌体展示文库,使用肽抗原从 ORF3a 重组表位中分离针对精心选择的 ORF3a 胞外 N 端和胞质 C 端结构域的结合物。使用酶联免疫吸附测定和表面等离子体共振分析进一步对这些结合物进行了表征,以评估它们与靶表位的结合亲和力。通过使用 ORF3a 转染细胞和 SARS-CoV-2 感染细胞的 Western blot 和荧光显微镜评估全长 ORF3a 蛋白的结合。还进行了共定位分析,以评估所选结合物作为 COVID-19 感染的潜在替代诊断或预后生物标志物的“配对潜力”。在我们的研究中鉴定了 ORF3a N 和 C 末端的表位特异性单克隆抗体。虽然肽的线性性质并不总是代表其在全长蛋白中的天然构象,但通过精心设计的选择方案,我们成功地分离出了能够识别跨膜蛋白暴露于感染细胞内部或外部的区域的抗 ORF3a 结合物。将讨论它们的治疗潜力。