Suppr超能文献

融合肽表位用于SARS-CoV-2抗体检测的高级多重血清学检测

Fusing Peptide Epitopes for Advanced Multiplex Serological Testing for SARS-CoV-2 Antibody Detection.

作者信息

Aldoukhi Ali H, Bilalis Panayiotis, Alhattab Dana M, Valle-Pérez Alexander U, Susapto Hepi H, Pérez-Pedroza Rosario, Backhoff-García Emiliano, Alsawaf Sarah M, Alshehri Salwa, Boshah Hattan, Alrashoudi Abdulelah A, Aljabr Waleed A, Alaamery Manal, Alrashed May, Hasanato Rana M, Farzan Raed A, Alsubki Roua A, Moretti Manola, Abedalthagafi Malak S, Hauser Charlotte A E

机构信息

Laboratory for Nanomedicine, Division of Biological and Environmental Science and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.

Computational Bioscience Research Center (CBRC), King Abdullah University of Science and Technology, Thuwal 23955-69900, Saudi Arabia.

出版信息

ACS Bio Med Chem Au. 2023 Aug 30;4(1):37-52. doi: 10.1021/acsbiomedchemau.3c00010. eCollection 2024 Feb 21.

Abstract

The tragic COVID-19 pandemic, which has seen a total of 655 million cases worldwide and a death toll of over 6.6 million seems finally tailing off. Even so, new variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continue to arise, the severity of which cannot be predicted in advance. This is concerning for the maintenance and stability of public health, since immune evasion and increased transmissibility may arise. Therefore, it is crucial to continue monitoring antibody responses to SARS-CoV-2 in the general population. As a complement to polymerase chain reaction tests, multiplex immunoassays are elegant tools that use individual protein or peptide antigens simultaneously to provide a high level of sensitivity and specificity. To further improve these aspects of SARS-CoV-2 antibody detection, as well as accuracy, we have developed an advanced serological peptide-based multiplex assay using antigen-fused peptide epitopes derived from both the spike and the nucleocapsid proteins. The significance of the epitopes selected for antibody detection has been verified by in silico molecular docking simulations between the peptide epitopes and reported SARS-CoV-2 antibodies. Peptides can be more easily and quickly modified and synthesized than full length proteins and can, therefore, be used in a more cost-effective manner. Three different fusion-epitope peptides (FEPs) were synthesized and tested by enzyme-linked immunosorbent assay (ELISA). A total of 145 blood serum samples were used, compromising 110 COVID-19 serum samples from COVID-19 patients and 35 negative control serum samples taken from COVID-19-free individuals before the outbreak. Interestingly, our data demonstrate that the sensitivity, specificity, and accuracy of the results for the FEP antigens are higher than for single peptide epitopes or mixtures of single peptide epitopes. Our FEP concept can be applied to different multiplex immunoassays testing not only for SARS-CoV-2 but also for various other pathogens. A significantly improved peptide-based serological assay may support the development of commercial point-of-care tests, such as lateral-flow-assays.

摘要

新冠疫情悲剧性地蔓延,全球累计确诊6.55亿例,死亡人数超过660万,如今似乎终于逐渐平息。即便如此,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的新变种仍不断出现,其严重程度无法预先预测。这关乎公共卫生的维持与稳定,因为可能出现免疫逃逸和传播力增强的情况。因此,持续监测普通人群对SARS-CoV-2的抗体反应至关重要。作为聚合酶链反应检测的补充,多重免疫测定是一种精巧的工具,它同时使用单个蛋白质或肽抗原,以提供高水平的灵敏度和特异性。为进一步提升SARS-CoV-2抗体检测的这些方面以及准确性,我们开发了一种先进的基于血清学肽的多重测定法,该方法使用源自刺突蛋白和核衣壳蛋白的抗原融合肽表位。通过肽表位与已报道的SARS-CoV-2抗体之间的计算机分子对接模拟,验证了所选用于抗体检测的表位的重要性。与全长蛋白质相比,肽更容易、更快速地进行修饰和合成,因此可以更具成本效益地使用。合成了三种不同的融合表位肽(FEP),并通过酶联免疫吸附测定(ELISA)进行测试。总共使用了145份血清样本,其中包括110份来自新冠患者的新冠血清样本和35份在疫情爆发前取自未感染新冠个体的阴性对照血清样本。有趣的是,我们的数据表明,FEP抗原检测结果的灵敏度、特异性和准确性高于单个肽表位或单个肽表位混合物。我们的FEP概念不仅可应用于针对SARS-CoV-2的不同多重免疫测定,还可应用于针对各种其他病原体的检测。一种显著改进的基于肽的血清学测定法可能会支持诸如侧流测定法等商业即时检测的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1afb/10885102/8e3419c93791/bg3c00010_0002.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验