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Updated: Nov 14, 2025

In Vitro Disassembly of Influenza A Virus Capsids by Gradient Centrifugation
Published on: March 27, 2016
A Dynamic, Supramolecular View on the Multivalent Interaction between Influenza Virus and Host Cell
Nico J Overeem1, Erhard van der Vries2,3, Jurriaan Huskens1
1Department of Molecules and Materials, MESA+ Institute for Nanotechnology, Faculty of Science and Technology, University of Twente, P.O. Box 217, Enschede, 7500 AE, The Netherlands.
Influenza viruses use multivalent interactions to bind host cells, enabling mucus traversal and cell entry. This dynamic process is crucial for understanding viral zoonotic potential and developing treatments.
Area of Science:
- Virology
- Biophysics
- Molecular Biology
Background:
- Influenza virus entry into host cells is critical for infection and disease spread.
- Surface proteins hemagglutinin and neuraminidase mediate virus-host cell interactions.
- Multivalent interactions with sialic acid glycans are key to viral adhesion.
Purpose of the Study:
- To review mechanisms of influenza virus mucus traversal and host cell recognition.
- To discuss the role of multivalent interactions in viral entry.
- To propose a model for influenza virus-induced cell entry.
Main Methods:
- Review of existing literature on influenza virus-host interactions.
- Analysis of techniques for measuring viral avidity and receptor specificity.
- Discussion of biophysical principles governing multivalent binding.
Main Results:
- Influenza viruses utilize superselective binding through multivalent interactions.
- Virus-induced receptor clustering facilitates cell entry.
- A dynamic balance between binding and cleaving maintains viral interactions.
Conclusions:
- Multivalent interactions are pivotal for influenza virus mucus penetration and host cell entry.
- Understanding these interactions is essential for assessing zoonotic risk and developing antivirals.
- Virus-induced receptor clustering represents a key step in initiating cell entry.
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