Jung Jaeyong, Kwon Soonil, Sung Jeong Soo, Bae Hyung Eun, Kang Min-Jung, Jose Joachim, Lee Misu, Pyun Jae-Chul
Department of Materials Science and Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.
Korea Institute of Science and Technology (KIST), Seoul 02456, Korea.
ACS Pharmacol Transl Sci. 2024 Nov 19;7(12):3914-3920. doi: 10.1021/acsptsci.4c00441. eCollection 2024 Dec 13.
For the prevention of SARS-CoV-2 infection, four Fv-antibodies with binding affinity for the ACE2 receptor were screened from an Fv-antibody library. The screened Fv-antibodies were expressed as soluble proteins and estimated to have a high binding affinity, comparable to that between SARS-CoV-2 and the ACE2 receptor. The interaction between the Fv-antibodies and the ACE2 receptor was analyzed using docking simulation, and the significant binding affinity of the screened Fv-antibodies was attributed to the homology in amino acid sequence with the ACE2 receptor. The neutralizing activities of the Fv-antibodies were demonstrated using a cell-based infection assay based on four pseudo-virus types with SARS-CoV-2 variant spike proteins (Wild-type D614, Delta B.1.617.2, and Omicron BA.2, and Omicron BA.4/5).
为预防新型冠状病毒(SARS-CoV-2)感染,从一个Fv抗体库中筛选出了四种对血管紧张素转换酶2(ACE2)受体具有结合亲和力的Fv抗体。筛选出的Fv抗体被表达为可溶性蛋白,据估计具有较高的结合亲和力,与SARS-CoV-2和ACE2受体之间的亲和力相当。使用对接模拟分析了Fv抗体与ACE2受体之间的相互作用,筛选出的Fv抗体具有显著的结合亲和力归因于其与ACE2受体氨基酸序列的同源性。使用基于四种带有SARS-CoV-2变异刺突蛋白(野生型D614、德尔塔B.1.617.2、奥密克戎BA.2以及奥密克戎BA.4/5)的假病毒类型的细胞感染试验,证明了Fv抗体的中和活性。