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

How fast does the GluR1Qflip channel open?

Gang Li1, Li Niu

  • 1Department of Chemistry and the Center for Neuroscience Research, State University of New York, Albany, New York 12222, USA.

The Journal of Biological Chemistry
|November 12, 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

Macrophage apoptosis in advanced atherosclerosis.

Annals of the New York Academy of Sciences·2009
Same author

Calcium/calmodulin-dependent protein kinase II links ER stress with Fas and mitochondrial apoptosis pathways.

The Journal of clinical investigation·2009
Same author

Cripto-1 overexpression is involved in the tumorigenesis of nasopharyngeal carcinoma.

BMC cancer·2009
Same author

Range of motion and orientation of the lumbar facet joints in vivo.

Spine·2009
Same author

[Silencing of COX-2 in nasopharyngeal carcinoma cells with a shRNAmir lentivirus vector].

Nan fang yi ke da xue xue bao = Journal of Southern Medical University·2009
Same author

The risk of melamine-induced nephrolithiasis in young children starts at a lower intake level than recommended by the WHO.

Pediatric nephrology (Berlin, Germany)·2009
Same journal

YhbO is a DJ-1 family glyoxalase and α-oxoaldehyde hydratase that confers resistance to reactive carbonyl stress (112).

The Journal of biological chemistry·2026
Same journal

ARMH3 acts as a central scaffold at the Golgi/TGN through interactions with Arl5, GBF1, and PI4KB.

The Journal of biological chemistry·2026
Same journal

PAX8 controls proximal tubule epithelial identity and stress response through epigenetic modification of distal regulatory elements.

The Journal of biological chemistry·2026
Same journal

Saturated cardiolipins are potent disruptors of inner mitochondrial membrane structure and function.

The Journal of biological chemistry·2026
Same journal

Phosphate release from myosin Va occurs after the initial powerstroke but before the secondary powerstroke associated with ADP-release.

The Journal of biological chemistry·2026
Same journal

Epigenetic silencing of miR-141 via core promoter methylation is associated with short-term bladder cancer progression.

The Journal of biological chemistry·2026
See all related articles

Researchers studied the GluR1Qflip channel, a key component in transmitting neural signals. They found this ion channel opens rapidly upon glutamate binding, enabling swift signal transduction.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Biophysics

Background:

  • Ligand-gated ion channels are crucial for neurotransmission, converting chemical signals into electrical ones.
  • The alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunit GluR1Qflip plays a vital role in this process.

Purpose of the Study:

  • To investigate the kinetics of the opening and closing of the GluR1Qflip channel.
  • To determine the temporal efficiency of GluR1Qflip in signal transduction.

Main Methods:

  • Utilized laser-pulse photolysis of caged glutamate to rapidly release glutamate.
  • Measured channel opening and closing rate constants using electrophysiological techniques.

Main Results:

Related Experiment Videos

  • The GluR1Qflip channel opened with a rate constant of (2.9 ± 0.2) x 10^4 s^-1 and closed with a rate constant of (2.1 ± 0.1) x 10^3 s^-1.
  • The shortest observed rise time for channel opening was 35 microseconds, significantly faster than previously reported.
  • The minimal kinetic model suggests binding of two glutamate molecules is required for channel opening with a probability of 0.93 ± 0.10.
  • Conclusions:

    • GluR1Qflip is a highly temporally efficient receptor for glutamate.
    • This receptor rapidly transduces glutamate binding into an electrical impulse, highlighting its importance in fast synaptic transmission.