Author: Watanabe, Tomoko; Takeda, Ko; Hiemori, Keiko; Minamisawa, Toshikazu; Tateno, Hiroaki
Title: A glycosaminoglycan microarray identifies the binding of SARSâ€CoVâ€2 spike protein to chondroitin sulfate E Cord-id: vrr1zh72 Document date: 2021_8_17
ID: vrr1zh72
Snippet: Heparan sulfate (HS), a sulfated glycosaminoglycan (GAG), was reported to be a necessary host attachment factor that promotes SARSâ€CoVâ€2 infection. In this study, we developed GAG microarrays based on fluorescence detection for highâ€sensitivity screening of the GAGâ€binding specificity of proteins and applied it for the analysis of SARSâ€CoVâ€2 spike (S) protein. Among the 20 distinct GAGs, the S protein bound not only to heparin (HEP)/HS but also to chondroitin sulfate E (CSE) in a con
Document: Heparan sulfate (HS), a sulfated glycosaminoglycan (GAG), was reported to be a necessary host attachment factor that promotes SARSâ€CoVâ€2 infection. In this study, we developed GAG microarrays based on fluorescence detection for highâ€sensitivity screening of the GAGâ€binding specificity of proteins and applied it for the analysis of SARSâ€CoVâ€2 spike (S) protein. Among the 20 distinct GAGs, the S protein bound not only to heparin (HEP)/HS but also to chondroitin sulfate E (CSE) in a concentrationâ€dependent manner. We then analyzed the specificity of each subunit of the S protein. While the S1 subunit showed exclusive binding to HEP, the S2 subunit also bound to CSE and HEP/HS. CSE might act as an alternative attachment factor for HS in SARSâ€CoVâ€2 infection.
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