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A glycosaminoglycan microarray identifies the binding of SARS-CoV-2 spike protein to chondroitin sulfate E
FEBS Letters ( IF 3.0 ) Pub Date : 2021-08-10 , DOI: 10.1002/1873-3468.14173
Tomoko Watanabe 1 , Ko Takeda 2 , Keiko Hiemori 1 , Toshikazu Minamisawa 2 , Hiroaki Tateno 1
Affiliation  

Heparan sulfate (HS), a sulfated glycosaminoglycan (GAG), was reported to be a necessary host attachment factor that promotes SARS-CoV-2 infection. In this study, we developed GAG microarrays based on fluorescence detection for high-sensitivity screening of the GAG-binding specificity of proteins and applied it for the analysis of SARS-CoV-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 concentration-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 SARS-CoV-2 infection.

中文翻译:

糖胺聚糖微阵列识别 SARS-CoV-2 刺突蛋白与硫酸软骨素 E 的结合

据报道,硫酸乙酰肝素 (HS) 是一种硫酸化糖胺聚糖 (GAG),它是促进 SARS-CoV-2 感染的必要宿主附着因子。在本研究中,我们开发了基于荧光检测的 GAG 微阵列,用于高灵敏度筛选蛋白质的 GAG 结合特异性,并将其应用于 SARS-CoV-2 刺突 (S) 蛋白的分析。在 20 种不同的 GAG 中,S 蛋白不仅与肝素 (HEP)/HS 结合,而且以浓度依赖性方式与硫酸软骨素 E (CSE) 结合。然后我们分析了 S 蛋白每个亚基的特异性。虽然 S1 亚基显示出与 HEP 的排他性结合,但 S2 亚基也与 CSE 和 HEP/HS 结合。CSE 可能作为 SARS-CoV-2 感染中 HS 的替代附着因子。
更新日期:2021-09-27
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