Suppr超能文献

利用刺突蛋白受体结合域开发针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)及其奥密克戎变种的适配体,作为一种潜在的诊断工具和治疗剂。

Aptamer Development for SARS-CoV-2 and Omicron Variants Using the Spike Protein Receptor Binding Domain as a Potential Diagnostic Tool and Therapeutic Agent.

作者信息

Shekar Prasanna V, Kumar Anuj, Mulgaonkar Nirmitee, Kashyap Samneet, Choudhir Gourav, Fernando Sandun, Rustgi Sachin

机构信息

Department of Plant and Environmental Sciences, Clemson University Pee Dee Research and Education Center, Florence, SC 29506, USA.

Department of Microbiology and Immunology, Dalhousie University, Halifax, NS B3H 4R2, Canada.

出版信息

Biomolecules. 2025 Jun 1;15(6):805. doi: 10.3390/biom15060805.

Abstract

Despite various methods for detecting and treating SARS-CoV-2, affordable and easily applicable solutions are still needed. Aptamers can potentially fill this gap. Here, we establish a workflow to identify aptamers that bind to the spike proteins of SARS-CoV-2, a process applicable to other targets as well. The spike protein is crucial for the virus's entry into host cells. The aptamer development process for the spike protein's receptor binding domain (RBD) begins with splitting the SARS-CoV-2's genome into 40 nucleotide-long sequences, predicting their two-dimensional structure, and sorting based on the free energy. Selected oligomers undergo three-dimensional structure prediction and docking onto the viral spike protein's RBD. Six RNA oligomers were identified as top candidates based on the RNA docking with the SARS-CoV-2 wild-type (WT) (Wuhan-Hu-1 strain) and Omicron variant BA.1 RBD and molecular dynamics simulations. Three oligomers also demonstrated strong predicted binding affinity with other SARS-CoV-2 variants, including BA.2, XBB.1.5, and EG.5, based on the protein-aptamer docking followed by stability evaluation using the MD simulations. The aptamer with the best fit for the spike protein RBD was later validated using biolayer interferometry. The process has resulted in identifying a single aptamer from a library of 29,000 RNA oligomers, which exhibited affinity in the submicromolar range and the potential to develop into a viral screen or therapeutic.

摘要

尽管有多种检测和治疗新冠病毒(SARS-CoV-2)的方法,但仍需要价格亲民且易于应用的解决方案。适配体有可能填补这一空白。在此,我们建立了一个工作流程来鉴定与SARS-CoV-2刺突蛋白结合的适配体,该过程也适用于其他靶点。刺突蛋白对于病毒进入宿主细胞至关重要。针对刺突蛋白受体结合域(RBD)的适配体开发过程始于将SARS-CoV-2的基因组切割成40个核苷酸长的序列,预测其二维结构,并基于自由能进行筛选。选定的寡聚物进行三维结构预测并与病毒刺突蛋白的RBD进行对接。基于与SARS-CoV-2野生型(WT)(武汉-1株)和奥密克戎变种BA.1 RBD的RNA对接以及分子动力学模拟,六种RNA寡聚物被确定为顶级候选物。基于蛋白质-适配体对接,随后使用分子动力学模拟进行稳定性评估,三种寡聚物还显示出与其他SARS-CoV-2变种(包括BA.2、XBB.1.5和EG.5)有很强的预测结合亲和力。后来使用生物层干涉术验证了与刺突蛋白RBD最匹配的适配体。该过程从一个包含29,000个RNA寡聚物的文库中鉴定出了一种单一适配体,其表现出亚微摩尔范围内的亲和力以及开发成病毒筛查或治疗方法的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d86c/12191217/fdc6248e5ad4/biomolecules-15-00805-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验