作者
Meghan E Garrett, Jared Galloway, Helen Y Chu, Hannah L Itell, Caitlin I Stoddard, Caitlin R Wolf, Jennifer K Logue, Dylan McDonald, Haidyn Weight, Frederick A Matsen, Julie Overbaugh
发表日期
2021/5/27
期刊
Cell
卷号
184
期号
11
页码范围
2927-2938. e11
出版商
Elsevier
简介
Defining long-term protective immunity to SARS-CoV-2 is one of the most pressing questions of our time and will require a detailed understanding of potential ways this virus can evolve to escape immune protection. Immune protection will most likely be mediated by antibodies that bind to the viral entry protein, spike (S). Here, we used Phage-DMS, an approach that comprehensively interrogates the effect of all possible mutations on binding to a protein of interest, to define the profile of antibody escape to the SARS-CoV-2 S protein using coronavirus disease 2019 (COVID-19) convalescent plasma. Antibody binding was common in two regions, the fusion peptide and the linker region upstream of the heptad repeat region 2. However, escape mutations were variable within these immunodominant regions. There was also individual variation in less commonly targeted epitopes. This study provides a granular view of …
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