The glycosylation in SARS-CoV-2 and its receptor ACE2.

The glycosylation in SARS-CoV-2 and its receptor ACE2.
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SARS-CoV-2 及其受体 ACE2 的糖基化

DOI:
10.1038/s41392-021-00809-8
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发表时间:
2021-11-15
影响因子:
39.3
通讯作者:
Tian Z
Tian Z
中科院分区:
医学1区
文献类型:
--
作者:
Gong Y;Qin S;Dai L;Tian Z

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截至2021年10月5日,2019冠状病毒病(COVID-19)是由严重急性呼吸道综合征冠状病毒2(SARS-CoV-2)引起的高度传染性疾病,已感染超过2.35亿人,并导致全球超过480万人死亡。冷冻电镜和拓扑学研究表明,SARS-CoV-2基因组编码大量糖基化蛋白,如刺突蛋白(S)、囊膜蛋白(E)、膜蛋白(M)和ORF 3a蛋白,这些蛋白与宿主的识别、穿透、结合、回收和致病有关。本文综述了SARS-CoV-2蛋白及其受体ACE 2糖基化的检测方法、作用底物、生物学功能,并对已批准和正在进行的SARS-CoV-2糖基化治疗药物进行了综述。本文的综述不仅可以拓宽对病毒糖生物学的理解,而且可以为开发针对SARS-CoV-2及其变体的新的预防和治疗方法提供关键线索。
Coronavirus disease 2019 (COVID-19), a highly infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has infected more than 235 million individuals and led to more than 4.8 million deaths worldwide as of October 5 2021. Cryo-electron microscopy and topology show that the SARS-CoV-2 genome encodes lots of highly glycosylated proteins, such as spike (S), envelope (E), membrane (M), and ORF3a proteins, which are responsible for host recognition, penetration, binding, recycling and pathogenesis. Here we reviewed the detections, substrates, biological functions of the glycosylation in SARS-CoV-2 proteins as well as the human receptor ACE2, and also summarized the approved and undergoing SARS-CoV-2 therapeutics associated with glycosylation. This review may not only broad the understanding of viral glycobiology, but also provide key clues for the development of new preventive and therapeutic methodologies against SARS-CoV-2 and its variants.
DOI: 10.1007/s13337-015-0293-5
发表时间: 2016-03
期刊: Virusdisease
影响因子: --
作者:
Banerjee N;Mukhopadhyay S
通讯作者: Mukhopadhyay S
对昆虫和人类细胞中产生的 SARS-CoV-2 刺突蛋白进行位点特异性 O 糖基化分析。
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发表时间: 2020-11-27
影响因子: 16.6
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发表时间: 2021-05
期刊: Nature chemistry
影响因子: 21.8
作者:
Ardejani MS;Noodleman L;Powers ET;Kelly JW
通讯作者: Kelly JW