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Potent peptidic fusion inhibitors of influenza virus
Open accessAbstract
Broadly reactive drugs for flu: Drugs for influenza are limited. For those available, viral resistance is rife. Part of the problem is that the virus is constantly mutating. Kadam et al. tested the cell entry stage of the virus life cycle as a drug target (see the Perspective by Whitehead). Cell entry is mediated by the major surface glycoprotein hemagglutinin (HA). This stage can be blocked by broadly neutralizing antibodies binding to HA. The authors generated small cyclic peptides that bind to the same sites on HA as the antibodies and mimic their activity. The peptides are cheap and easy to synthesize, are nontoxic to mice, and prevented infection of cells by many types of influenza virus. Science , this issue p. 496 ; see also p. 450
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“Protein1,5, peptide36 and small-molecule inhibitors37 have been designed to bind to the stem region of group 1 HA and neutralize influenza A viruses, but none recognize the group 2 HA.”
From Design of protein-binding proteins from the target structure alone (2022) · cites this paper as [36]
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Metadata
- Authors
- Kadam, R. U., Juraszek, J., Brandenburg, B., Buyck, C., Schepens, W. B. G., Kesteleyn, B., Stoops, B., Vreeken, R. J., Vermond, J., Goutier, W., Tang, C., Vogels, R., Friesen, R. H. E., Goudsmit, J., van Dongen, M. J. P., & Wilson, I. A.
- Affiliations
- Scripps Research Institute (US)
- Janssen (Netherlands) (NL)
- Janssen (Belgium) (BE)
- Harvard University (US)
- Janssen Prevention Center, Leiden, Netherlands.
- Corresponding author
- Kadam, Rameshwar U.
- Juraszek, Jarek
- Wilson, Ian A.
- ORCID
- Venue
- Science
- Published
- 2017-10-27
- Volume
- 358
- Issue
- 6362
- Pages
- 496-502
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC5659926
- OpenAlex
- W2759132244
- Cited by
- 165
- References
- 39
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 16 · 2023: 19 · 2022: 19 · 2021: 16 · 2020: 29 · 2019: 19 · 2018: 24 · 2017: 2
- FWCI
- 16.50
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (award304792, 1R56 AI117675, award348894, R56 AI127371)
- Topics
- Health Sciences › Medicine › Epidemiology › Influenza Virus Research Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
- Physical Sciences › Chemistry › Organic Chemistry › Carbohydrate Chemistry and Synthesis
- Keywords
- influenza virus, hemagglutinin, peptide inhibitors, fusion inhibitors, broadly neutralizing antibodies, hypervariable region, membrane fusion, 2009 H1N1 pandemic, antiviral agents
- MeSH terms
- Animals, Antiviral Agents, Humans, Male, Mice, Inbred BALB C, Peptides, Cyclic, Protein Conformation, Drug Design, Crystallography, X-Ray, Complementarity Determining Regions, Mice, Influenza A Virus, H1N1 Subtype, Influenza A Virus, H5N1 Subtype, Virus Internalization, Antibodies, Neutralizing
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