tetano
Editor, Senior Moderator
J Biol Chem. 2018 Aug 3. pii: jbc.RA118.004012. doi: 10.1074/jbc.RA118.004012. [Epub ahead of print]
[h=1]Structural analyses reveal the mechanism of inhibition of influenza virus NS1 by two antiviral compounds.[/h] Kleinpeter AB[SUP]1[/SUP], Jureka AS[SUP]1[/SUP], Falahat SM[SUP]1[/SUP], Green TJ[SUP]2[/SUP], Petit CM[SUP]3[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The influenza virus is a significant public health concern causing 250,000-500,000 deaths worldwide each year. Its ability to change quickly results in the potential for rapid generation of pandemic strains for which most individuals would have no antibody protection. This pandemic potential highlights the need for the continuous development of new drugs against influenza virus. As an essential component, and well-established virulence determinant, the non-structural protein 1 (NS1) of influenza virus is a highly prioritized target for the development of anti-influenza compounds. Here, we used NMR to determine that the NS1 effector domain (NS1[SUP]ED[/SUP]) derived from the A/Brevig Mission/1/1918 (H1N1) strain of influenza (1918[SUP]H1N1[/SUP]) binds to two previously described anti-influenza compounds A9 (JJ3297) and A22. We then used X-ray crystallography to determine the three-dimensional structure of the 1918[SUP]H1N1[/SUP] NS1[SUP]ED[/SUP] Furthermore, we mapped the A9/A22-binding site onto our 1918[SUP]H1N1[/SUP] NS1[SUP]ED[/SUP] structure and determined that A9 and A22 interact with the NS1[SUP]ED[/SUP] in the hydrophobic pocket known to facilitate binding to the 30 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF30), suggesting that the two compounds likely attenuate influenza replication by inhibiting the NS1[SUP]ED[/SUP]-CPSF30 interaction. Finally, our structure revealed that NS1[SUP]ED[/SUP] could dimerize via an interface that we termed the α[SUB]3[/SUB]-α[SUB]3[/SUB] dimer. Taken together, the findings presented here provide strong evidence for the mechanism of action of two anti-influenza compounds that target NS1 and contribute significant structural insights into NS1 that we hope will promote and inform the development and optimization of influenza therapies based on A9/A22.
[h=4]KEYWORDS:[/h] 1918 H1N1; 2013 H7N9; CPSF30; NS1; antiviral agent; influenza; influenza virus; non-structural protein 1; nuclear magnetic resonance (NMR); protein structure; viral protein; viral replication
PMID: 30076219 DOI: 10.1074/jbc.RA118.004012
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[h=1]Structural analyses reveal the mechanism of inhibition of influenza virus NS1 by two antiviral compounds.[/h] Kleinpeter AB[SUP]1[/SUP], Jureka AS[SUP]1[/SUP], Falahat SM[SUP]1[/SUP], Green TJ[SUP]2[/SUP], Petit CM[SUP]3[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] The influenza virus is a significant public health concern causing 250,000-500,000 deaths worldwide each year. Its ability to change quickly results in the potential for rapid generation of pandemic strains for which most individuals would have no antibody protection. This pandemic potential highlights the need for the continuous development of new drugs against influenza virus. As an essential component, and well-established virulence determinant, the non-structural protein 1 (NS1) of influenza virus is a highly prioritized target for the development of anti-influenza compounds. Here, we used NMR to determine that the NS1 effector domain (NS1[SUP]ED[/SUP]) derived from the A/Brevig Mission/1/1918 (H1N1) strain of influenza (1918[SUP]H1N1[/SUP]) binds to two previously described anti-influenza compounds A9 (JJ3297) and A22. We then used X-ray crystallography to determine the three-dimensional structure of the 1918[SUP]H1N1[/SUP] NS1[SUP]ED[/SUP] Furthermore, we mapped the A9/A22-binding site onto our 1918[SUP]H1N1[/SUP] NS1[SUP]ED[/SUP] structure and determined that A9 and A22 interact with the NS1[SUP]ED[/SUP] in the hydrophobic pocket known to facilitate binding to the 30 kDa subunit of the cleavage and polyadenylation specificity factor (CPSF30), suggesting that the two compounds likely attenuate influenza replication by inhibiting the NS1[SUP]ED[/SUP]-CPSF30 interaction. Finally, our structure revealed that NS1[SUP]ED[/SUP] could dimerize via an interface that we termed the α[SUB]3[/SUB]-α[SUB]3[/SUB] dimer. Taken together, the findings presented here provide strong evidence for the mechanism of action of two anti-influenza compounds that target NS1 and contribute significant structural insights into NS1 that we hope will promote and inform the development and optimization of influenza therapies based on A9/A22.
[h=4]KEYWORDS:[/h] 1918 H1N1; 2013 H7N9; CPSF30; NS1; antiviral agent; influenza; influenza virus; non-structural protein 1; nuclear magnetic resonance (NMR); protein structure; viral protein; viral replication
PMID: 30076219 DOI: 10.1074/jbc.RA118.004012
Free full text