生物
病毒学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
Sars病毒
2019年冠状病毒病(COVID-19)
2019-20冠状病毒爆发
倍他科诺病毒
医学
疾病
爆发
病理
传染病(医学专业)
作者
Alexander Lacrampe,Fenghua Hu
出处
期刊:Cell
[Elsevier]
日期:2023-08-01
卷期号:186 (16): 3329-3331
被引量:3
标识
DOI:10.1016/j.cell.2023.07.005
摘要
The lysosomal membrane protein TMEM106B functions as a proviral factor in SARS-CoV-2 infection, though it was not known how. In this issue of Cell, Baggen et al. demonstrate that TMEM106B serves as an ACE2-independent receptor for SARS-CoV-2 entry by promoting the fusion of the viral membrane with the lysosomal membrane. The lysosomal membrane protein TMEM106B functions as a proviral factor in SARS-CoV-2 infection, though it was not known how. In this issue of Cell, Baggen et al. demonstrate that TMEM106B serves as an ACE2-independent receptor for SARS-CoV-2 entry by promoting the fusion of the viral membrane with the lysosomal membrane. TMEM106B is a receptor mediating ACE2-independent SARS-CoV-2 cell entryBaggen et al.CellJuly 7, 2023In BriefThe lysosomal transmembrane protein TMEM106B can serve as an alternative receptor for SARS-CoV-2 entry into ACE2-negative cells. Spike substitution E484D improves spike binding to TMEM106B, enhancing TMEM106B-mediated SARS-CoV-2 infection. Full-Text PDF Open Access
科研通智能强力驱动
Strongly Powered by AbleSci AI