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 Concept Videos

Ligand-Gated Ion Channel Receptor: Gating Mechanism01:30

Ligand-Gated Ion Channel Receptor: Gating Mechanism

Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow the influx of ions across the membrane once the neurotransmitter binds, allowing the subsequent transmission of electrical excitation across the neurons. Other ligand-gated ion channels, like the γ-aminobutyric acid (GABA) receptor, permit anions like chloride into the cells on the binding of the GABA molecule. Their entry into the cell...

You might also read

Related Articles

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

Sort by
Same author

Intravital Multimodal Imaging of Human Cortical Organoid Transplantation in a Mouse Model of Chronic Stroke.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026
Same author

Critical period plasticity enables credit assignment.

bioRxiv : the preprint server for biology·2026
Same author

Implications of systolic pulmonary artery pressure trajectories in systemic lupus erythematosus-associated pulmonary hypertension: a CSTAR-PAH cohort study.

Frontiers in immunology·2026
Same author

Author Correction: Cerebellar aging is spatially heterogeneous and supports cognitive resilience in later life.

Nature neuroscience·2026
Same author

A sensitive orange fluorescent calcium ion indicator for imaging neural activity.

Nature communications·2026
Same author

Tunable Bessel beam two-photon fluorescence microscopy for high-speed volumetric imaging of brain dynamics.

eLife·2026

Related Experiment Video

Updated: May 8, 2026

In vivo Neuronal Calcium Imaging in C. elegans
11:06

In vivo Neuronal Calcium Imaging in C. elegans

Published on: April 10, 2013

25.0K

Fast and sensitive GCaMP calcium indicators for imaging neural populations.

Yan Zhang1, Márton Rózsa1,2, Yajie Liang1,3,4

  • 1Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.

Nature
|March 16, 2023
PubMed
Summary

Researchers developed new jGCaMP8 sensors for faster and more sensitive neural activity tracking. These protein-based calcium sensors enable observing large neuron populations at speeds relevant to brain computation.

More Related Videos

Imaging Mitochondrial Ca2+ Uptake in Astrocytes and Neurons using Genetically Encoded Ca2+ Indicators GECIs
07:46

Imaging Mitochondrial Ca2+ Uptake in Astrocytes and Neurons using Genetically Encoded Ca2+ Indicators GECIs

Published on: January 22, 2022

4.2K
Subcellular Imaging of Neuronal Calcium Handling In Vivo
07:14

Subcellular Imaging of Neuronal Calcium Handling In Vivo

Published on: March 17, 2023

1.3K

Related Experiment Videos

Last Updated: May 8, 2026

In vivo Neuronal Calcium Imaging in C. elegans
11:06

In vivo Neuronal Calcium Imaging in C. elegans

Published on: April 10, 2013

25.0K
Imaging Mitochondrial Ca2+ Uptake in Astrocytes and Neurons using Genetically Encoded Ca2+ Indicators GECIs
07:46

Imaging Mitochondrial Ca2+ Uptake in Astrocytes and Neurons using Genetically Encoded Ca2+ Indicators GECIs

Published on: January 22, 2022

4.2K
Subcellular Imaging of Neuronal Calcium Handling In Vivo
07:14

Subcellular Imaging of Neuronal Calcium Handling In Vivo

Published on: March 17, 2023

1.3K

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Biochemistry

Background:

  • Protein-based calcium indicators are crucial for monitoring neural activity in vivo.
  • Existing sensors face limitations in speed and sensitivity, hindering the study of rapid neural processes.

Purpose of the Study:

  • To develop and optimize novel GCaMP-type calcium indicators with improved kinetics and sensitivity.
  • To create sensors capable of tracking neural activity at timescales relevant to neural computation.

Main Methods:

  • Large-scale screening of protein variants.
  • Structure-guided mutagenesis of GCaMP-type indicators.
  • Biochemical and functional characterization of developed sensors.

Main Results:

  • Developed jGCaMP8 sensors with ultra-fast kinetics (2 ms half-rise time).
  • Achieved the highest sensitivity reported for protein-based calcium sensors.
  • Demonstrated suitability for tracking large neuronal populations at relevant timescales.

Conclusions:

  • jGCaMP8 sensors represent a significant advancement in calcium imaging technology.
  • These sensors overcome previous limitations, enabling more precise studies of neural dynamics.
  • The enhanced performance of jGCaMP8 will facilitate breakthroughs in understanding neural computation.