University of Groningen
Membrane fusion of influenza and chikungunya viruses
Blijleven, Jelle
IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below.
Document Version
Publisher's PDF, also known as Version of record
Publication date: 2018
Link to publication in University of Groningen/UMCG research database
Citation for published version (APA):
Blijleven, J. (2018). Membrane fusion of influenza and chikungunya viruses: Mechanisms inferred from single-particle experiments. Rijksuniversiteit Groningen.
Copyright
Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).
Take-down policy
If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.
Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.
128
Summary for non-experts
Viruses depend on a host for their continued existence: they invade a host cell and hijack its machinery to produce new virus particles. In this thesis we studied two virus species that infect humans. Influenza virus (“the flu”) causes yearly epidemics due to its ability to extensively change appearance; this continuous shapeshifting makes the threat of a new, deadly influenza pandemic real. Chikungunya virus has recently spread across the globe and is transmitted by mosquitos whose range expands with global warming. Full protection or treatment against ei-ther virus remain unavailable. Both viruses have an envelope, a membrane wrapping the viral contents. A key step in entry is the merger of the viral envelope with the envelope that covers cells. Protein spikes on the outside of the virus mediate this fusion event. In the process, the proteins extend and grab the target membrane after which they fold back onto themselves. Thereby, they force both membranes to come together and merge, mixing the viral contents into the cell. This thesis focuses on determining the mechanisms that these proteins use to achieve entry. We use a microscopy technique that allows us to observe the behavior of indi-vidual virus particles. By controlling the experimental conditions and using agents that block fusion, new insight was obtained on the way these proteins function, and specifically, how mul-tiple spike proteins need to work together to mediate fusion. Such knowledge of the exact mechanisms involved in viral fusion will help to guide the design of new antiviral therapeutics.
