Department of Chemistry and Biochemistry, Jackson State University, Jackson, Mississippi 39217, United States.
Department of Microbiology and Immunology, University of Mississippi Medical Center, Jackson, Mississippi 39216, United States.
J Phys Chem Lett. 2021 Mar 4;12(8):2166-2171. doi: 10.1021/acs.jpclett.0c03570. Epub 2021 Feb 25.
The ongoing outbreak of the coronavirus infection has killed more than 2 million people. Herein, we demonstrate that Rhodamine 6G (Rh-6G) dye conjugated DNA aptamer-attached gold nanostar (GNS)-based distance-dependent nanoparticle surface energy transfer (NSET) spectroscopy has the capability of rapid diagnosis of specific SARS-CoV-2 spike recombinant antigen or SARS-CoV-2 spike protein pseudotyped baculovirus within 10 min. Because Rh-6G-attached single-stand DNA aptamer wrapped the GNS, 99% dye fluorescence was quenched because of the NSET process. In the presence of spike antigen or virus, the fluorescence signal persists because of the aptamer-spike protein binding. Specifically, the limit of detection for the NSET assay has been determined to be 130 fg/mL for antigen and 8 particles/mL for virus. Finally, we have demonstrated that DNA aptamer-attached GNSs can stop virus infection by blocking the angiotensin-converting enzyme 2 (ACE2) receptor binding capability and destroying the lipid membrane of the virus.
正在爆发的冠状病毒感染已导致超过 200 万人死亡。在此,我们证明 Rhodamine 6G(Rh-6G)染料偶联的 DNA 适体连接的金纳米星(GNS)基于距离依赖的纳米粒子表面能量转移(NSET)光谱法具有在 10 分钟内快速诊断特定的 SARS-CoV-2 刺突重组抗原或 SARS-CoV-2 刺突蛋白假型杆状病毒的能力。由于 Rh-6G 偶联的单链 DNA 适体包裹了 GNS,99%的染料荧光因 NSET 过程而被猝灭。在存在刺突抗原或病毒的情况下,由于适体-刺突蛋白结合,荧光信号得以持续。具体而言,NSET 测定法的检测限已确定为抗原 130 fg/mL,病毒 8 个颗粒/mL。最后,我们已经证明,DNA 适体连接的 GNS 可以通过阻断血管紧张素转换酶 2(ACE2)受体结合能力和破坏病毒的脂质膜来阻止病毒感染。