tetano
Editor, Senior Moderator
J Struct Biol. 2016 Dec 19. pii: S1047-8477(16)30253-2. doi: 10.1016/j.jsb.2016.12.007. [Epub ahead of print]
[h=1]Structural studies of influenza virus RNPs by electron microscopy indicate molecular contortions within NP supra-structures.[/h] Gallagher JR[SUP]1[/SUP], Torian U[SUP]1[/SUP], McCraw DM[SUP]1[/SUP], Harris AK[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Ribonucleoprotein (RNP) complexes of influenza viruses are composed of multiple copies of the viral nucleoprotein (NP) that can form filamentous supra-structures. RNPs package distinct viral genomic RNA segments of different lengths into pleomorphic influenza virions. RNPs also function in viral RNA transcription and replication. Different RNP segments have varying lengths, but all must be incorporated into virions during assembly and then released during viral entry for productive infection cycles. RNP structures serve varied functions in the viral replication cycle, therefore understanding their molecular organization and flexibility is essential to understanding these functions. Here, we show using electron tomography and image analyses that isolated RNP filaments are not rigid helical structures, but instead display variations in lengths, curvatures, and even tolerated kinks and local unwinding. Additionally, we observed NP rings within RNP preparations, which were commonly composed of 5, 6, or 7 NP molecules and were of similar widths to filaments, suggesting plasticity in NP-NP interactions mediate RNP structural polymorphism. To demonstrate that NP alone could generate rings of variable oligomeric state, we performed 2D single particle image analysis on recombinant NP and found that rings of 4 and 5 protomers dominated, but rings of all compositions up to 7 were directly observed with variable frequency. This structural flexibility may be needed as RNPs carry out the interactions and conformational changes required for RNP assembly and genome packaging as well as virus uncoating.
Copyright ? 2016. Published by Elsevier Inc.
[h=4]KEYWORDS:[/h] Electron microscopy; Flexibility; Influenza virus; RNPs; Structure; Tomography
PMID: 28007449 DOI: 10.1016/j.jsb.2016.12.007
[PubMed - as supplied by publisher]
[h=1]Structural studies of influenza virus RNPs by electron microscopy indicate molecular contortions within NP supra-structures.[/h] Gallagher JR[SUP]1[/SUP], Torian U[SUP]1[/SUP], McCraw DM[SUP]1[/SUP], Harris AK[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Ribonucleoprotein (RNP) complexes of influenza viruses are composed of multiple copies of the viral nucleoprotein (NP) that can form filamentous supra-structures. RNPs package distinct viral genomic RNA segments of different lengths into pleomorphic influenza virions. RNPs also function in viral RNA transcription and replication. Different RNP segments have varying lengths, but all must be incorporated into virions during assembly and then released during viral entry for productive infection cycles. RNP structures serve varied functions in the viral replication cycle, therefore understanding their molecular organization and flexibility is essential to understanding these functions. Here, we show using electron tomography and image analyses that isolated RNP filaments are not rigid helical structures, but instead display variations in lengths, curvatures, and even tolerated kinks and local unwinding. Additionally, we observed NP rings within RNP preparations, which were commonly composed of 5, 6, or 7 NP molecules and were of similar widths to filaments, suggesting plasticity in NP-NP interactions mediate RNP structural polymorphism. To demonstrate that NP alone could generate rings of variable oligomeric state, we performed 2D single particle image analysis on recombinant NP and found that rings of 4 and 5 protomers dominated, but rings of all compositions up to 7 were directly observed with variable frequency. This structural flexibility may be needed as RNPs carry out the interactions and conformational changes required for RNP assembly and genome packaging as well as virus uncoating.
Copyright ? 2016. Published by Elsevier Inc.
[h=4]KEYWORDS:[/h] Electron microscopy; Flexibility; Influenza virus; RNPs; Structure; Tomography
PMID: 28007449 DOI: 10.1016/j.jsb.2016.12.007
[PubMed - as supplied by publisher]