N121T and N121S substitutions on the SARS‐CoV‐2 spike protein impact on serum neutralization

Author:

Lo Van Thi1,Lim Hyun A.1,Jang Seong Sik1,Kim Min Chan1,Chamfort Alain Chrysler1,Kim Ha Yeon1,Mun Da Young1,Kang Min Chang1,Lee Han Byul1,Kim Sunjoo2,Lee Younghee1,Park Sangkyu1ORCID,Yoon Sun‐Woo3,Kim Hye Kwon1

Affiliation:

1. Department of Biological Science and Biotechnology College of Natural Science, Chungbuk National University Cheongju South Korea

2. Department of Laboratory Medicine Gyeongsang National University Changwon Hospital Changwon South Korea

3. Department of Vaccine Biotechnology Andong National University Andong South Korea

Abstract

AbstractThe N121 site on the spike protein of SARS‐CoV‐2 is associated with heme and its metabolite, biliverdin, which can affect antibody binding. Both N121T and N121S substitutions have been observed in natural conditions and in a hamster model of dual infection with SARS‐CoV‐2 and Influenza A virus. Serum pseudotype neutralization assays against HIV‐1 particles carrying wild‐type, N121T, and N121S spikes with immune mouse and human sera revealed that N121T and N121S mutations had a greater impact on serum neutralization than biliverdin treatment. Although N121T and N121S substitutions are not currently major SARS‐CoV‐2 variants of concern, this study could provide fundamental information to prepare for potential future mutations at the N121 site of SARS‐CoV‐2.

Funder

Ministry of Science and ICT, South Korea

National Research Foundation of Korea

Publisher

Wiley

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