Development of a bispecific nanobody conjugate broadly neutralizes diverse SARS-CoV-2 variants and structural basis for its broad neutralization.
Abstrak
The continuous emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants with increased transmissibility and profound immune-escape capacity makes it an urgent need to develop broad-spectrum therapeutics. Nanobodies have recently attracted extensive attentions due to their excellent biochemical and binding properties. Here, we report two high-affinity nanobodies (Nb-015 and Nb-021) that target non-overlapping epitopes in SARS-CoV-2 S-RBD. Both nanobodies could efficiently neutralize diverse viruses of SARS-CoV-2. The neutralizing mechanisms for the two nanobodies are further delineated by high-resolution nanobody/S-RBD complex structures. In addition, an Fc-based tetravalent nanobody format is constructed by combining Nb-015 and Nb-021. The resultant nanobody conjugate, designated as Nb-X2-Fc, exhibits significantly enhanced breadth and potency against all-tested SARS-CoV-2 variants, including Omicron sub-lineages. These data demonstrate that Nb-X2-Fc could serve as an effective drug candidate for the treatment of SARS-CoV-2 infection, deserving further in-vivo evaluations in the future.
Topik & Kata Kunci
Penulis (22)
Jing Yang
Sheng Lin
Zimin Chen
Fanli Yang
Liyan Guo
Lingling Wang
Yanping Duan
Xindan Zhang
Yushan Dai
Keqing Yin
Chongzhang Yu
Xin Yuan
Honglu Sun
Bin He
Yu Cao
Haoyu Ye
Haohao Dong
Xianbo Liu
Bo Chen
Jian Li
Qi Zhao
Guangwen Lu
Akses Cepat
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- 2023
- Sumber Database
- DOAJ
- DOI
- 10.1371/journal.ppat.1011804
- Akses
- Open Access ✓