Human antibodies to SARS-CoV-2 with a recurring YYDRxG motif retain binding and neutralization to variants of concern including Omicron

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作者
Hejun Liu
Chengzi I. Kaku
Ge Song
Meng Yuan
Raiees Andrabi
Dennis R. Burton
Laura M. Walker
Ian A. Wilson
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[1] The Scripps Research Institute,Department of Integrative Structural and Computational Biology
[2] Adimab,Department of Immunology and Microbiology
[3] LLC,The Skaggs Institute for Chemical Biology
[4] The Scripps Research Institute,undefined
[5] Ragon Institute of MGH,undefined
[6] MIT and Harvard,undefined
[7] Adagio Therapeutics,undefined
[8] Inc,undefined
[9] The Scripps Research Institute,undefined
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Studying the antibody response to SARS-CoV-2 informs on how the human immune system can respond to antigenic variants as well as other SARS-related viruses. Here, we structurally identified a YYDRxG motif encoded by IGHD3-22 in CDR H3 that facilitates antibody targeting to a functionally conserved epitope on the SARS-CoV-2 receptor binding domain. A computational search for a YYDRxG pattern in publicly available sequences uncovered 100 such antibodies, many of which can neutralize SARS-CoV-2 variants and SARS-CoV. Thus, the YYDRxG motif represents a common convergent solution for the human humoral immune system to target sarbecoviruses including the Omicron variant. These findings suggest an epitope-targeting strategy to identify potent and broadly neutralizing antibodies for design of pan-sarbecovirus vaccines and antibody therapeutics.
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