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一种硫酸化鲍鱼多糖在体外抑制SARS-CoV-2对Vero E6细胞的感染。

A Sulfated Abalone Polysaccharide Inhibited SARS-CoV-2 Infection of Vero E6 Cells In Vitro.

作者信息

Sun Jinghe, Song Shuang, Ai Chunqing, Zhu Beiwei, Yang Jingfeng

机构信息

Collaborative Innovation Center of Seafood Deep Processing, National Engineering Research Center of Seafood, School of Food Science and Technology, Dalian Polytechnic University, Dalian 116034, China.

出版信息

Foods. 2022 Sep 16;11(18):2865. doi: 10.3390/foods11182865.

Abstract

Sulfate polysaccharides, such as heparin sulfate, have been found to have inhibitory activity against SARS-CoV-2. An abalone polysaccharide, AGSP, was deeply sulfate modified using the chlorosulfonic acid/pyridine method, yielding S-AGSP. AGSP and S-AGSP inhibitions of SARS-CoV-2 infection of Vero E6 cells were tested in vitro. The interference of AGSP or S-AGSP on the binding interaction between the SARS-CoV-2 spike protein and angiotensin-converting enzyme was tested using a biolayer interferometry assay. Results showed that S-AGSP, above a concentration of 1.87 µg/mL, significantly inhibited SARS-CoV-2 infection of Vero E6 cells. Compared with AGSP, S-AGSP obviously weakened the affinity between the SARS-CoV-2 spike protein and ACE2. The polysaccharide's sulfate content played a vital role in influencing the binding affinity of spike protein to ACE2. Therefore, S-AGSP has potential as a COVID-19 competitive inhibitor as well as a candidate to be repurposed as a prophylactic COVID-19 therapeutic.

摘要

硫酸多糖,如硫酸肝素,已被发现对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)具有抑制活性。一种鲍鱼多糖AGSP,采用氯磺酸/吡啶法进行深度硫酸化修饰,得到S-AGSP。在体外测试了AGSP和S-AGSP对Vero E6细胞感染SARS-CoV-2的抑制作用。使用生物层干涉测定法测试了AGSP或S-AGSP对SARS-CoV-2刺突蛋白与血管紧张素转换酶之间结合相互作用的干扰。结果表明,浓度高于1.87μg/mL时,S-AGSP能显著抑制Vero E6细胞感染SARS-CoV-2。与AGSP相比,S-AGSP明显削弱了SARS-CoV-2刺突蛋白与血管紧张素转换酶2(ACE2)之间的亲和力。多糖的硫酸含量在影响刺突蛋白与ACE2的结合亲和力方面起着至关重要的作用。因此,S-AGSP有潜力作为一种新型冠状病毒肺炎(COVID-19)竞争性抑制剂,以及作为一种重新用于COVID-19预防治疗的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65cb/9498428/50ea090c7d58/foods-11-02865-g001.jpg

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