Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Viral membrane fusion.

Stephen C Harrison1

  • 1Jack and Eileen Connors Structural Biology Laboratory, Harvard Medical School, Laboratory of Molecular Medicine, Children's Hospital Boston, Howard Hughes Medical Institute, 250 Longwood Avenue, Boston, MA 02115, USA. harrison@crystal.harvard.edu

Nature Structural & Molecular Biology
|July 4, 2008
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Structures of folding intermediates on BAM show diverse substrates fold by a conserved mechanism.

Proceedings of the National Academy of Sciences of the United States of America·2026
Same author

Mechanism of membrane perforation in rotavirus cell entry.

bioRxiv : the preprint server for biology·2026
Same author

Structures of folding intermediates on BAM show diverse substrates fold by a uniform mechanism.

bioRxiv : the preprint server for biology·2025
Same author

A coordinated kinase and phosphatase network regulates Stu2 recruitment to yeast kinetochores.

The Journal of cell biology·2025
Same author

Fluorescence-barcoded cell lines stably expressing membrane-anchored influenza neuraminidases.

Vaccine·2025
Same author

Fluorescence-barcoded cell lines stably expressing membrane-anchored influenza neuraminidases.

bioRxiv : the preprint server for biology·2025
Same journal

Genome-wide absolute quantification of chromatin looping.

Nature structural & molecular biology·2026
Same journal

Distinct ATRX functions cooperate with 9-1-1 and CST complexes to safeguard replication and telomere integrity.

Nature structural & molecular biology·2026
Same journal

Structurally defining neurokinin selectivity to improve NK2R agonists.

Nature structural & molecular biology·2026
Same journal

Structural basis of asymmetric transcription through a composite nucleosome formed by a hexasome and an octasome.

Nature structural & molecular biology·2026
Same journal

Structural basis of AtCas9 recognition of PAM mutants in underwound DNA topology.

Nature structural & molecular biology·2026
Same journal

Catalytic activation of human Argonaute 2 requires RNA duplex deformation.

Nature structural & molecular biology·2026
See all related articles

Viral fusion proteins mediate infection by merging viral and cell membranes. Despite structural diversity, these proteins share a common mechanism triggered by ligands, leading to membrane fusion. Fusion inhibitors show antiviral potential.

Area of Science:

  • Virology
  • Structural Biology
  • Biochemistry

Background:

  • Viral infection relies on the fusion of viral and host cell membranes.
  • Viral fusion proteins are essential mediators of this membrane fusion process.
  • These proteins undergo significant structural changes to facilitate bilayer merging.

Purpose of the Study:

  • To elucidate the common mechanism of viral membrane fusion mediated by viral fusion proteins.
  • To illustrate how diverse viral fusion protein structures implement a conserved fusion mechanism.
  • To highlight the potential of fusion inhibitors as antiviral agents.

Main Methods:

  • Comparative analysis of viral fusion protein structures and mechanisms.
  • Detailed examination of influenza virus hemagglutinin.

Related Experiment Videos

  • In-depth review of flavivirus E protein and vesicular stomatitis virus G protein functions.
  • Main Results:

    • Viral fusion proteins, despite structural variations, share a common ligand-triggered conformational change mechanism.
    • This conformational change drives the apposition and merger of viral and cellular membranes.
    • Examples like influenza HA, flavivirus E, and VSV G proteins exemplify diverse structural solutions to achieve fusion.

    Conclusions:

    • Viral fusion proteins utilize a conserved mechanism involving conformational changes to achieve membrane fusion.
    • Structural diversity in viral fusion proteins reflects convergent evolution towards a common functional goal.
    • Targeting viral fusion proteins with inhibitors presents a viable strategy for antiviral therapy.