Sun Miao, Wu Zijing, Zhang Jialu, Chen Mingying, Lu Yao, Yang Chaoyong, Song Yanling
The MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, State Key Laboratory of Physical Chemistry of Solid Surfaces, Department of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Institute of Molecular Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.
Nano Today. 2022 Jun;44:101499. doi: 10.1016/j.nantod.2022.101499. Epub 2022 May 6.
Recently, the SARS-CoV-2 Omicron has spread very quickly worldwide. Several studies have indicated that the Omicron variant causes a substantial evasion of the humoral immune response and the majority of existing SARS-CoV-2 neutralizing antibodies. Here we address this challenge by applying a spherical cocktail neutralizing aptamer-gold nanoparticle (SNAP) to block the interaction of Omicron receptor binding domain (RBD) and host Angiotensin-Converting Enzyme 2 (ACE2). With the synergetic blocking strategy based on multivalent multisite aptamer binding and steric hindrance by the size-matched gold scaffold, the SNAP conjugate tightly binds to Omicron RBD with a dissociation constant of 13.6 pM, almost completely blocking the infection of Omicron pseudovirus with a half-maximal inhibitory concentration of 35.9 pM. Overall, the SNAP strategy not only fills the gap of the humoral immune evasion caused by clustered mutations on Omicron, but also provides a clue for the development of new broad neutralizing reagents against future variants.
最近,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎毒株在全球范围内传播迅速。多项研究表明,奥密克戎变体导致体液免疫反应和大多数现有的SARS-CoV-2中和抗体出现显著逃逸。在此,我们通过应用球形鸡尾酒中和适配体-金纳米颗粒(SNAP)来阻断奥密克戎受体结合域(RBD)与宿主血管紧张素转换酶2(ACE2)的相互作用,以应对这一挑战。基于多价多位点适配体结合和尺寸匹配的金支架的空间位阻的协同阻断策略,SNAP偶联物以13.6 pM的解离常数紧密结合奥密克戎RBD,以35.9 pM的半数最大抑制浓度几乎完全阻断奥密克戎假病毒的感染。总体而言,SNAP策略不仅填补了奥密克戎上聚集突变导致的体液免疫逃逸的空白,也为开发针对未来变体的新型广谱中和试剂提供了线索。