Suppr超能文献

针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的广谱中和适体:一组多样化的修饰DNA抗病毒剂。

Broadly neutralizing aptamers to SARS-CoV-2: A diverse panel of modified DNA antiviral agents.

作者信息

Gelinas Amy D, Tan Tiong Kit, Liu Sai, Jaramillo Javier G, Chadwick James, Harding Adam C, Zhang Chi, Ream Brian E, Chase Chelsea N, Otis Matthew R, Lee Thomas, Schneider Daniel J, James William S, Janjic Nebojsa

机构信息

SomaLogic, Inc., 2945 Wilderness Place, Boulder, CO 80301, USA.

MRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford OX3 9DS, UK.

出版信息

Mol Ther Nucleic Acids. 2023 Mar 14;31:370-382. doi: 10.1016/j.omtn.2023.01.008. Epub 2023 Jan 21.

Abstract

Since its discovery, COVID-19 has rapidly spread across the globe and has had a massive toll on human health, with infection mortality rates as high as 10%, and a crippling impact on the world economy. Despite numerous advances, there remains an urgent need for accurate and rapid point-of-care diagnostic tests and better therapeutic treatment options. To contribute chemically distinct, non-protein-based affinity reagents, we report here the identification of modified DNA-based aptamers that selectively bind to the S1, S2, or receptor-binding domain of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein. Several aptamers inhibit the binding of the spike protein to its cell-surface receptor angiotensin-converting enzyme 2 (ACE2) and neutralize authentic SARS-CoV-2 virus , including all variants of concern. With a high degree of nuclease resistance imparted by the base modifications, these reagents represent a new class of molecules with potential for further development as diagnostics or therapeutics.

摘要

自发现以来,新型冠状病毒肺炎(COVID-19)已在全球迅速传播,对人类健康造成了巨大损失,感染死亡率高达10%,并对世界经济产生了严重影响。尽管取得了诸多进展,但仍迫切需要准确、快速的即时诊断测试和更好的治疗选择。为了提供化学性质不同的、非蛋白质类的亲和试剂,我们在此报告已鉴定出修饰的基于DNA的适体,它们能选择性结合严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白的S1、S2或受体结合结构域。几种适体可抑制刺突蛋白与其细胞表面受体血管紧张素转换酶2(ACE2)的结合,并中和真正的SARS-CoV-2病毒,包括所有令人关注的变异株。由于碱基修饰赋予了高度的核酸酶抗性,这些试剂代表了一类具有进一步开发为诊断或治疗药物潜力的新分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9565/9929607/5e57eea15c9a/fx1.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