tetano
Editor, Senior Moderator
Biophys J
. 2024 Nov 20:S0006-3495(24)00739-2.
doi: 10.1016/j.bpj.2024.11.016. Online ahead of print. A physical model for M1-mediated influenza A virus assembly
Julia Peukes[SUP] 1 [/SUP], Serge Dmitrieff[SUP] 2 [/SUP], François J Nédélec[SUP] 3 [/SUP], John A G Briggs[SUP] 4 [/SUP]
Affiliations
Influenza A virus particles assemble at the plasma membrane of infected cells. During assembly all components of the virus come together in a coordinated manner to deform the membrane into a protrusion eventually forming a new, membrane-enveloped virus. Here we integrate recent molecular insights of this process, particularly concerning the structure of the matrix protein 1 (M1), within a theoretical framework describing the mechanics of virus assembly. Our model describes M1 polymerization and membrane protrusion formation, explaining why it is efficient for M1 to form long strands assembling into helices in filamentous virions. Eventually, we find how the architecture of M1 helices is controlled by physical properties of viral proteins and the host cell membrane. Finally, by considering the growth force and speed of viral filaments, we propose that the helical geometry of M1 strands might have evolved to optimize for fast and efficient virus assembly and growth.
. 2024 Nov 20:S0006-3495(24)00739-2.
doi: 10.1016/j.bpj.2024.11.016. Online ahead of print. A physical model for M1-mediated influenza A virus assembly
Julia Peukes[SUP] 1 [/SUP], Serge Dmitrieff[SUP] 2 [/SUP], François J Nédélec[SUP] 3 [/SUP], John A G Briggs[SUP] 4 [/SUP]
Affiliations
- PMID: 39573879
- DOI: 10.1016/j.bpj.2024.11.016
Influenza A virus particles assemble at the plasma membrane of infected cells. During assembly all components of the virus come together in a coordinated manner to deform the membrane into a protrusion eventually forming a new, membrane-enveloped virus. Here we integrate recent molecular insights of this process, particularly concerning the structure of the matrix protein 1 (M1), within a theoretical framework describing the mechanics of virus assembly. Our model describes M1 polymerization and membrane protrusion formation, explaining why it is efficient for M1 to form long strands assembling into helices in filamentous virions. Eventually, we find how the architecture of M1 helices is controlled by physical properties of viral proteins and the host cell membrane. Finally, by considering the growth force and speed of viral filaments, we propose that the helical geometry of M1 strands might have evolved to optimize for fast and efficient virus assembly and growth.