SARS-CoV-2 has become a global pandemic threatening human health and safety.It is urgent to find effective therapeutic agents and targets with the continuous emergence of novel mutant strains.The knowledge of the mole...SARS-CoV-2 has become a global pandemic threatening human health and safety.It is urgent to find effective therapeutic agents and targets with the continuous emergence of novel mutant strains.The knowledge of the molecular basis and pathogenesis of SARS-CoV-2 in host cells requires to be understood comprehensively.The unknown structure and function of nsp2 have hindered our understanding of its role in SARS-CoV-2 infection.Here,we report the crystal structure of the N-terminal of SARS-CoV-2 nsp2 to a high resolution of 1.96?.This novel structure contains three zinc fingers,belonging to the C2 H2,C4,and C2 HC types,respectively.Structure analysis suggests that nsp2 may be involved in binding nucleic acids and regulating intracellular signaling pathways.The binding to single or double-stranded nucleic acids was mainly through the large positively charged region on the surface of nsp2,and K111,K112,K113 were key residues.Our findings lay the foundation for a better understanding of the relationship between structure and function for nsp2.It is helpful to make full use of nsp2 as further research and development of antiviral targets and drug design.展开更多
基金supported financially by National Key Research and Development Program of China(2018YFE0113100)National Natural Science Foundation of China(31872713)。
文摘SARS-CoV-2 has become a global pandemic threatening human health and safety.It is urgent to find effective therapeutic agents and targets with the continuous emergence of novel mutant strains.The knowledge of the molecular basis and pathogenesis of SARS-CoV-2 in host cells requires to be understood comprehensively.The unknown structure and function of nsp2 have hindered our understanding of its role in SARS-CoV-2 infection.Here,we report the crystal structure of the N-terminal of SARS-CoV-2 nsp2 to a high resolution of 1.96?.This novel structure contains three zinc fingers,belonging to the C2 H2,C4,and C2 HC types,respectively.Structure analysis suggests that nsp2 may be involved in binding nucleic acids and regulating intracellular signaling pathways.The binding to single or double-stranded nucleic acids was mainly through the large positively charged region on the surface of nsp2,and K111,K112,K113 were key residues.Our findings lay the foundation for a better understanding of the relationship between structure and function for nsp2.It is helpful to make full use of nsp2 as further research and development of antiviral targets and drug design.
