整合素
冠状病毒
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
严重急性呼吸综合征冠状病毒
血管紧张素转化酶2
2019年冠状病毒病(COVID-19)
大流行
肽
化学
细胞生物学
生物
医学
细胞
疾病
生物化学
传染病(医学专业)
内科学
作者
Brandon J. Beddingfield,Naoki Iwanaga,Prem P. Chapagain,Wenshu Zheng,Chad J. Roy,Ye Hu,Jay K. Kolls,Gregory Bix
标识
DOI:10.1016/j.jacbts.2020.10.003
摘要
Many efforts to design and screen therapeutics for the current severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) pandemic have focused on inhibiting viral host cell entry by disrupting angiotensin-converting enzyme-2 (ACE2) binding with the SARS-CoV-2 spike protein. This work focuses on the potential to inhibit SARS-CoV-2 entry through a hypothesized α5β1 integrin−based mechanism and indicates that inhibiting the spike protein interaction with α5β1 integrin (+/− ACE2) and the interaction between α5β1 integrin and ACE2 using a novel molecule (ATN-161) represents a promising approach to treat coronavirus disease-19.
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