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G-Protein Gated Ion Channels01:21

G-Protein Gated Ion Channels

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GPCRs are primarily responsible for our sense of smell, taste, and vision.  The binding of a sensory stimulus activates GPCR to stimulate effector proteins, many of which are ion channels in the sensory organs. GPCRs modulate the opening and closing of the target ion channels either directly by binding them, or by releasing second messengers that activate these channels. As ions move across the membrane, the membrane potential is altered, which induces an appropriate response.
Sensory...
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Channel Rhodopsins01:11

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Most organisms use photoreceptors to sense and respond to light. Examples of photoreceptors include bacteriorhodopsins and bacteriophytochromes in some bacteria, phytochromes in plants, and rhodopsins in the photoreceptor cells of the vertebral retina. The light-sensitive property of these receptors is because of the bound chromophores, such as bilin in the phytochromes and retinal in the rhodopsins.
Rhodopsins belong to the family of cell surface proteins called G-protein coupled receptors,...
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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...
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Related Experiment Video

Updated: Jul 11, 2025

Multi-photon Intracellular Sodium Imaging Combined with UV-mediated Focal Uncaging of Glutamate in CA1 Pyramidal Neurons
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Multi-photon Intracellular Sodium Imaging Combined with UV-mediated Focal Uncaging of Glutamate in CA1 Pyramidal Neurons

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Blue and Green Light Responsive Caged Glutamate.

Jingxuan Ma1, Nishal M Egodawaththa1, Charitha Guruge1

  • 1Department of Biomedical and Chemical Engineering and Sciences, Florida Institute of Technology, 150 West University Blvd., Melbourne, FL 32901, United States.

Journal of Photochemistry and Photobiology. A, Chemistry
|November 6, 2023
PubMed
Summary

New visible-light-activated glutamate (Glu) photocages offer precise control over neurotransmitter release for brain mapping. These cages overcome limitations of UV-based methods, enabling safer in vivo studies and potential modulation of both excitatory and inhibitory neurotransmission.

Keywords:
BODIPYCaged GluGlutamateVisible lightphoto-protecting groupphotoirradiation

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Methodology for Biomimetic Chemical Neuromodulation of Rat Retinas with the Neurotransmitter Glutamate In Vitro
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Methodology for Biomimetic Chemical Neuromodulation of Rat Retinas with the Neurotransmitter Glutamate In Vitro
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Methodology for Biomimetic Chemical Neuromodulation of Rat Retinas with the Neurotransmitter Glutamate In Vitro

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Area of Science:

  • Neuroscience
  • Photochemistry
  • Organic Synthesis

Background:

  • Glutamate (Glu) is a key excitatory neurotransmitter essential for memory formation.
  • Precise spatiotemporal control of Glu release is crucial for mapping neural pathways.
  • Existing Glu photocages often rely on UV light, posing cytotoxicity risks and limiting in vivo applications.

Purpose of the Study:

  • To develop novel glutamate photocages responsive to visible light for enhanced in vivo neuroscience research.
  • To synthesize and characterize new caged glutamate compounds with improved photophysical properties.
  • To enable optical control over neurotransmitter release using visible wavelengths.

Main Methods:

  • Synthesis of 11 novel glutamate photocages utilizing thiocoumarin and BODIPY scaffolds.
  • Photochemical studies to determine uncaging kinetics and quantum efficiencies (QE) for each derivative.
  • Evaluation of visible light (467 nm and 515-540 nm) responsiveness.

Main Results:

  • Efficient preparation of 11 caged Glu compounds responding to visible light.
  • Quantum efficiencies (Φ) ranged from 0.0001 to 0.65.
  • A novel BODIPY-based cage, Me-BODIPY-Br-Glu, demonstrated highly efficient Glu release (QE = 0.65).

Conclusions:

  • Developed visible-light-activated glutamate photocages offer precise spatiotemporal control.
  • These new cages overcome limitations of UV-based systems, reducing cytotoxicity.
  • The photocage design is extendable to other neurotransmitters like GABA, enabling dual optical control of neural activity.