Advanced Science (Jan 2022)
Neutralizing Antibodies to SARS‐CoV‐2 Selected from a Human Antibody Library Constructed Decades Ago
- Min Qiang,
- Peixiang Ma,
- Yu Li,
- Hejun Liu,
- Adam Harding,
- Chenyu Min,
- Fulian Wang,
- Lili Liu,
- Meng Yuan,
- Qun Ji,
- Pingdong Tao,
- Xiaojie Shi,
- Zhean Li,
- Teng Li,
- Xian Wang,
- Yu Zhang,
- Nicholas C. Wu,
- Chang‐Chun D. Lee,
- Xueyong Zhu,
- Javier Gilbert‐Jaramillo,
- Chuyue Zhang,
- Abhishek Saxena,
- Xingxu Huang,
- Hou Wang,
- William James,
- Raymond A. Dwek,
- Ian A. Wilson,
- Guang Yang,
- Richard A. Lerner
Affiliations
- Min Qiang
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Peixiang Ma
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Yu Li
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Hejun Liu
- Department of Integrative Structural and Computational Biology The Scripps Research Institute La Jolla CA 92037 USA
- Adam Harding
- Sir William Dunn School of Pathology University of Oxford Oxford OX1 3RE UK
- Chenyu Min
- Velox Pharmaceuticals Changzhou 213000 P. R. China
- Fulian Wang
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Lili Liu
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Meng Yuan
- Department of Integrative Structural and Computational Biology The Scripps Research Institute La Jolla CA 92037 USA
- Qun Ji
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Pingdong Tao
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Xiaojie Shi
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Zhean Li
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Teng Li
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Xian Wang
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Yu Zhang
- School of Life Science and Technology ShanghaiTech University Shanghai 201210 P. R. China
- Nicholas C. Wu
- Department of Integrative Structural and Computational Biology The Scripps Research Institute La Jolla CA 92037 USA
- Chang‐Chun D. Lee
- Department of Integrative Structural and Computational Biology The Scripps Research Institute La Jolla CA 92037 USA
- Xueyong Zhu
- Department of Integrative Structural and Computational Biology The Scripps Research Institute La Jolla CA 92037 USA
- Javier Gilbert‐Jaramillo
- Sir William Dunn School of Pathology University of Oxford Oxford OX1 3RE UK
- Chuyue Zhang
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Abhishek Saxena
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Xingxu Huang
- School of Life Science and Technology ShanghaiTech University Shanghai 201210 P. R. China
- Hou Wang
- ShOx Science Limited Shanghai 200135 P. R. China
- William James
- Sir William Dunn School of Pathology University of Oxford Oxford OX1 3RE UK
- Raymond A. Dwek
- Department of Biochemistry Oxford Glycobiology Institute South Parks Road Oxford OX1 3QU UK
- Ian A. Wilson
- Department of Integrative Structural and Computational Biology The Scripps Research Institute La Jolla CA 92037 USA
- Guang Yang
- Shanghai Institute for Advanced Immunochemical Studies ShanghaiTech University Shanghai 201210 P. R. China
- Richard A. Lerner
- Department of Chemistry The Scripps Research Institute La Jolla CA 92037 USA
- DOI
- https://doi.org/10.1002/advs.202102181
- Journal volume & issue
-
Vol. 9,
no. 1
pp. n/a – n/a
Abstract
Abstract Combinatorial antibody libraries not only effectively reduce antibody discovery to a numbers game, but enable documentation of the history of antibody responses in an individual. The severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) pandemic has prompted a wider application of this technology to meet the public health challenge of pandemic threats in the modern era. Herein, a combinatorial human antibody library constructed 20 years before the coronavirus disease 2019 (COVID‐19) pandemic is used to discover three highly potent antibodies that selectively bind SARS‐CoV‐2 spike protein and neutralize authentic SARS‐CoV‐2 virus. Compared to neutralizing antibodies from COVID‐19 patients with generally low somatic hypermutation (SHM), these three antibodies contain over 13–22 SHMs, many of which are involved in specific interactions in their crystal structures with SARS‐CoV‐2 spike receptor binding domain. The identification of these somatically mutated antibodies in a pre‐pandemic library raises intriguing questions about the origin and evolution of these antibodies with respect to their reactivity with SARS‐CoV‐2.
Keywords
- antibody–antigen interaction
- combinatorial antibody library
- COVID‐19
- neutralizing antibody
- SARS‐CoV‐2
- somatic hypermutation