4.4 Article

Curvature Sensing by a Viral Scission Protein

Journal

BIOCHEMISTRY
Volume 55, Issue 25, Pages 3493-3496

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biochem.6b00539

Keywords

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Funding

  1. Medical Research Council [MR/L00870X/1, MR/L018578/1]
  2. European Union Seventh Framework Programme [FP7-PEOPLE-2012-CIG: 333955]
  3. Wenner-Gren Foundations
  4. Swedish Foundation for Strategic Research via the Center for Biomembrane Research
  5. MRC [MR/L018578/1, MR/L00870X/1] Funding Source: UKRI
  6. Medical Research Council [MR/L018578/1, MR/L00870X/1] Funding Source: researchfish

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Membrane scission is the final step in all budding processes wherein a membrane neck is sufficiently constricted so as to allow for fission and the release of the budded particle. For influenza viruses, membrane scission is mediated by an amphipathic helix (AH) domain in the viral M2 protein. While it is known that the M2AH alters membrane curvature, it is not known how the protein is localized to the center neck of budding virions where it would be able to cause membrane scission. Here, we use molecular dynamics simulations on buckled lipid bilayers to show that the M2AH senses membrane curvature and preferentially localizes to regions of high membrane curvature, comparable to that seen at the center neck of budding influenza viruses. These results were then validated using in vitro binding assays to show that the M2AH senses membrane curvature by detecting lipid packing defects in the membrane. Our results show that the M2AH senses membrane curvature and suggest that the AH domain may localize the protein at the viral neck where it can then mediate membrane scission and the release of budding viruses.

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