2022
DOI: 10.1134/s0006297922110116
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Cationic Channelrhodopsin from the Alga Platymonas subcordiformis as a Promising Optogenetic Tool

Abstract: The progress in optogenetics largely depends on the development of light-activated proteins as new molecular tools. Using cultured hippocampal neurons, we compared the properties of two light-activated cation channels – classical channelrhodopsin-2 from Chlamydomonas reinhardtii (CrChR2) and recently described channelrhodopsin isolated from the alga Platymonas subcordiformis (PsChR2). PsChR2 ensured generation of action potentials by neurons when activated by the pulsed light stimulation with the frequencies u… Show more

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Cited by 3 publications
(2 citation statements)
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“…To circumvent this problem, we decided to use an optogenetic approach for the tetanization of neurons. Classical channelrhodopsin2, due to the pronounced sensitization of responses during rhythmic stimulation, allows for the induction of controlled bursts of action potentials at frequencies up to 20-30 Hz, but not higher [31]. Therefore, we used the fast channelrhodopsin oChIEF, which allows the efficient optogenetic stimulation of neurons at frequencies around 100 Hz [32], thus allowing us to reproduce conventional plasticity-induction protocols.…”
Section: Resultsmentioning
confidence: 99%
“…To circumvent this problem, we decided to use an optogenetic approach for the tetanization of neurons. Classical channelrhodopsin2, due to the pronounced sensitization of responses during rhythmic stimulation, allows for the induction of controlled bursts of action potentials at frequencies up to 20-30 Hz, but not higher [31]. Therefore, we used the fast channelrhodopsin oChIEF, which allows the efficient optogenetic stimulation of neurons at frequencies around 100 Hz [32], thus allowing us to reproduce conventional plasticity-induction protocols.…”
Section: Resultsmentioning
confidence: 99%
“…To circumvent this problem, we decided to use an optogenetic approach for tetanization of neurons. Classical channelrhodopsin2, due to the pronounced sensitization of responses during rhythmic stimulation, allows to induce controlled bursts of action potentials at frequencies up to 20-30 Hz, but not higher [33]. Therefore, we used the fast channelrhodopsin oChIEF , which allows efficient optogenetic stimulation of neurons at frequencies around 100 Hz [34], thus letting us to reproduce conventional plasticity-induction protocols.…”
Section: Resultsmentioning
confidence: 99%