Opsins

Opsins are light-sensitive proteins that convert photons into cellular signals, forming the molecular basis of vision and other photoreceptive functions across animals and microorganisms. Each opsin binds a retinal chromophore; photon absorption changes retinal’s shape, alters the protein’s conformation, and initiates signaling through G proteins or ion channels, depending on the opsin family. In neuroscience, opsins help explain how photoreceptors encode light intensity, color, and timing, while engineered microbial opsins provide tools for optogenetics, allowing researchers to activate or inhibit selected neurons with light. Their study links molecular photochemistry to sensory processing and circuit function.

Opsins - Related Videos

Research

JoVE Journal - Biochemistry

Methodology for Studying Interactions of Vitamin A Membrane Receptors and Opsin Protein with their Ligands in Generating the Retinylidene Protein

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Cited by 3 •

2024

Here, we describe two quantitative methods for studying the protein-ligand interactions of vitamin A membrane receptors and photoreceptor opsin with their respective physiological ligands.

Research

JoVE Journal - Biology
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In vitro Investigation of the MexAB Efflux Pump From Pseudomonas aeruginosa

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Cited by 11 •

2014

We present a protocol for the in vitro investigation of efflux pumps from Pseudomonas aeruginosa. This protocol allows for the generation of a robust, reversible, and tunable proton gradient within the liposome membrane and hence should be adaptable to any membrane protein energized by the protomotive force.

Research

JoVE Journal - Neuroscience
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A Method for High Fidelity Optogenetic Control of Individual Pyramidal Neurons In vivo

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Cited by 2 •

2013

The recent development of neuroscience tools that combine genetics and optics, termed "optogenetics", enables control over neural circuit activity with an unprecedented level of spatial and temporal resolution. Here we provide a protocol for integrating in vivo recording with optogenetic manipulation of genetically-defined subsets of prefrontal cortical and subicular pyramidal neurons.

A Fluorescence-based Assay of Phospholipid Scramblase Activity

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Cited by 61 •

2016

We describe a fluorescence-based assay to measure phospholipid scrambling in large unilamellar liposomes reconstituted with opsin.

Research

JoVE Journal - Biology
Free Sample

Targeted DNA Methylation Analysis by Next-generation Sequencing

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Cited by 83 •

2015

Bisulfite amplicon sequencing (BSAS) is a method for quantifying cytosine methylation in targeted genomic regions of interest. This method uses bisulfite conversion paired with PCR amplification of target regions prior to next-generation sequencing to produce absolute quantitation of DNA methylation at a base-specific level.

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