Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 130 Meilong Rd., Shanghai 200237, China.
Department of Pathogen Biology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin 300070, China.
J Am Chem Soc. 2024 Jul 31;146(30):21017-21024. doi: 10.1021/jacs.4c06172. Epub 2024 Jul 19.
The devastating COVID-19 pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has made society acutely aware of the urgency in developing effective techniques to timely monitor the outbreak of previously unknown viral species as well as their mutants, which could be even more lethal and/or contagious. Here, we report a fluorogenic sensor array consisting of peptides truncated from the binding domain of human angiotensin-converting enzyme 2 (hACE2) for SARS-CoV-2. A set of five fluorescently tagged peptides were used to construct the senor array in the presence of different low-dimensional quenching materials. When orthogonally incubated with the wild-type SARS-CoV-2 and its variants of concern (VOCs), the fluorescence of each peptide probe was specifically recovered, and the different recovery rates provide a "fingerprint" characteristic of each viral strain. This, in turn, allows them to be differentiated from each other using principal component analysis. Interestingly, the classification result from our sensor array agrees well with the evolutionary relationship similarity of the VOCs. This study offers insight into the development of effective sensing tools for highly contagious viruses and their mutants based on rationally truncating peptide ligands from human receptors.
由严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2)引起的毁灭性 COVID-19 大流行,使社会深刻意识到开发有效技术以实时监测先前未知病毒物种及其突变体的紧迫性,这些病毒突变体可能更具致命性和/或传染性。在这里,我们报告了一种由人血管紧张素转换酶 2(hACE2)结合域截断的肽组成的荧光传感器阵列,用于 SARS-CoV-2。使用一组五个荧光标记的肽在存在不同低维猝灭材料的情况下构建传感器阵列。当与野生型 SARS-CoV-2 及其关注的变异株(VOCs)正交孵育时,每个肽探针的荧光都特异性恢复,并且不同的恢复率提供了每个病毒株的“指纹”特征。这反过来又可以使用主成分分析将它们彼此区分开来。有趣的是,我们传感器阵列的分类结果与 VOCs 的进化关系相似性很好。这项研究为基于从人类受体合理截断肽配体来开发针对高传染性病毒及其突变体的有效传感工具提供了思路。