Review of COVID-19 Antibody Therapies

Author:

Chen Jiahui1,Gao Kaifu1,Wang Rui1,Nguyen Duc Duy2,Wei Guo-Wei134

Affiliation:

1. Department of Mathematics, Michigan State University, East Lansing, Michigan 48824, USA;

2. Department of Mathematics, University of Kentucky, Lexington, Kentucky 40506, USA

3. Department of Electrical and Computer Engineering, Michigan State University, East Lansing, Michigan 48824, USA

4. Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824, USA

Abstract

In the global health emergency caused by coronavirus disease 2019 (COVID-19), efficient and specific therapies are urgently needed. Compared with traditional small-molecular drugs, antibody therapies are relatively easy to develop; they are as specific as vaccines in targeting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2); and they have thus attracted much attention in the past few months. This article reviews seven existing antibodies for neutralizing SARS-CoV-2 with 3D structures deposited in the Protein Data Bank (PDB). Five 3D antibody structures associated with the SARS-CoV spike (S) protein are also evaluated for their potential in neutralizing SARS-CoV-2. The interactions of these antibodies with the S protein receptor-binding domain (RBD) are compared with those between angiotensin-converting enzyme 2 and RBD complexes. Due to the orders of magnitude in the discrepancies of experimental binding affinities, we introduce topological data analysis, a variety of network models, and deep learning to analyze the binding strength and therapeutic potential of the 14 antibody–antigen complexes. The current COVID-19 antibody clinical trials, which are not limited to the S protein target, are also reviewed.

Publisher

Annual Reviews

Subject

Cell Biology,Biochemistry,Bioengineering,Structural Biology,Biophysics

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