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

Interactions between synaptic vesicle fusion proteins explored by atomic force microscopy.

A Yersin1, H Hirling, P Steiner

  • 1Laboratoire de Neurobiologie Cellulaire, Faculté des Sciences de la Vie, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland. alexandre.yersin@epfl.ch

Proceedings of the National Academy of Sciences of the United States of America
|July 11, 2003
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

The watchmaker's eye: Exposure keratopathy with secondary limbal stem cell deficiency due to the use of a loupe.

Journal francais d'ophtalmologie·2025
Same author

Effect of antibiotics on mechanical properties of Bordetella pertussis examined by atomic force microscopy.

Micron (Oxford, England : 1993)·2022
Same author

A simple liquid state <sup>1</sup>H NMR measurement to directly determine the surface hydroxyl density of porous silica.

Chemical communications (Cambridge, England)·2021
Same author

Patient Portals: Objectives, Acceptance, and Effects on Health Outcome - A Scoping Review of Reviews.

Studies in health technology and informatics·2021
Same author

First record of Diaphanosoma spinulosum Herbst 1975 (Cladocera: Sididae) for inland water bodies of Ecuador.

Brazilian journal of biology = Revista brasleira de biologia·2020
Same author

Nanomotion detection based on atomic force microscopy cantilevers.

Cell surface (Amsterdam, Netherlands)·2020

Researchers measured SNARE complex interactions using atomic force microscopy to understand neurotransmitter release. Findings suggest a minimum of four complexes are needed for fusion and reveal how regulatory proteins and toxins affect this process.

Area of Science:

  • Molecular biology
  • Biophysics
  • Neuroscience

Background:

  • Macromolecular complex biophysical properties are challenging to measure.
  • The SNARE complex is crucial for synaptic vesicle docking and fusion.
  • Understanding SNARE complex function is key to neurotransmission.

Purpose of the Study:

  • To measure interaction forces and kinetics of SNARE complex components.
  • To elucidate the sequence of SNARE complex assembly and function.
  • To investigate the effects of regulatory proteins and toxins on SNARE complex formation and activity.

Main Methods:

  • Reconstitution of the synaptic SNARE complex in an atomic force microscope.
  • Measurement of specific interaction forces and dissociation kinetics between SNARE proteins.

Related Experiment Videos

  • On-line registration of tetanus toxin protease activity on the SNARE complex.
  • Main Results:

    • Determined specific interaction forces and dissociation kinetics of SNARE components.
    • Proposed a sequence of SNARE interactions essential for fusion.
    • Demonstrated that neuronal Sec1 inhibits SNARE complex formation.
    • Measured the effect of tetanus toxin protease on SNARE complex activity.

    Conclusions:

    • A minimum of four SNARE complexes are likely necessary for synaptic vesicle fusion.
    • Regulatory proteins like neuronal Sec1 and toxins like tetanus toxin significantly modulate SNARE complex function.
    • These findings provide a basis for studying protein microdomains and screening drugs targeting protein-protein interactions.