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                <identifier>oai:data.mendeley.com/wdsystvjng.1</identifier>
                <datestamp>2021-09-15T21:30:43Z</datestamp>
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    <dc:creator>wang, jian</dc:creator>
    <dc:title>An antibody-based proximity labelling map reveals mechanisms of SARS-CoV-2 inhibition of antiviral immunity. Zhang et al.</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>The global epidemic caused by the coronavirus SARS-CoV-2 has resulted in the infection of over 200 million people. To extend the knowledge of interactions between SARS-CoV-2 and humans, we systematically investigate the interactome of 29 viral proteins in human cells by using an antibody-based TurboID assay. In total, 1388 high-confidence human proximal proteins with biotinylated sites are identified. Notably, we find that SARS-CoV-2 manipulates the antiviral and immune responses. We validate that the membrane protein ITGB1 associates ACE2 to mediate SARS-CoV-2 entry. Moreover, we reveal that SARS-CoV-2 proteins inhibit activation of the interferon pathway through the mitochondrial protein MAVS and the methyltransferase SETD2. We propose 111 potential drugs for the clinical treatment of COVID-19 and identify three compounds that significantly inhibit the replication of SARS-CoV-2. The proximity labelling map of SARS-CoV-2 and humans provides a resource for elucidating the mechanisms of viral infection and developing drugs for COVID-19 treatment.</dc:description>
    <dc:subject>Medicine</dc:subject>
    <dc:subject>Life Sciences</dc:subject>
    <dc:subject>Interactome</dc:subject>
    <dc:subject>Interaction Proteomics</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/wdsystvjng.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/wdsystvjng.1</dc:identifier>
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    <dc:date>2021-09-15T21:30:43Z</dc:date>
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