Halo Tag: Difference between revisions
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== | ==APhotoswitchable HaloTag for Spatiotemporal Control of Fluorescence in Living Cells== | ||
==== Claire Deo, Franziska Walterspiel, Begoña Ugarte-Uribe | <StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''> | ||
== Claire Deo, Franziska Walterspiel, Begoña Ugarte-Uribe == | |||
==[https://onlinelibrary.wiley.com/share/ZFYT2R9ZRCUTJRHQZCRW?target=10.1002/anie.202424955]. ([https://doi.org/10.1002/anie.202424955 DOI: 10.1002/anie.202424955])== | |||
---- | The Photoswitchable Halo Tag (psHaloTag) is a unique chemigenetic system designed to provide reversible, light-controlled fluorescence tunable through both genetic and synthetic modifications, with promising applications for dynamic imaging in biological microscopy <ref>https://doi.org/10.1002/anie.202424955</ref>. psHaloTag addresses a major gap in the availability of reliable, reversible systems suitable for live-cell imaging. Many current systems are limited in tracking long-term, cyclical processes or in refreshing the pool of observable molecules. psHaloTag combines the genetically encoded HaloTag protein with the light-sensing sAsLOV2 domain. When illuminated with 450 nm light, psHaloTag undergoes a reversible change that activates a bound rhodamine dye ligand, resulting in a significant increase in fluorescence. This strong, multiple-cycle reporter overcomes the limitations of irreversible systems. It is an important tool for achieving precise spatiotemporal control in demanding applications such as live-cell Super-Resolution Microscopy (SMLM), where many established photosensitive probes cannot be reactivated. | ||
==== Function ==== | |||
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The | The psHaloTag works as an allosteric photoswitch. | ||
*Protein Scaffold: An engineered HaloTag protein with the light-sensing sAsLOV2 domain. | |||
*Ligand: Binds to a fluorogenic rhodamine dye (e.g., JF635-HTL). | |||
:Light ON (450 nm): Light activates the sAsLOV2 domain using FMN cofactor, causing a conformational change (Jα helix unfolding). | |||
:Fluorescence ON: This change forces the bound dye into its fluorescent state. | |||
:Light OFF (Dark): The protein structure relaxes back to its original shape, shifting the dye back to its non-fluorescent state. | |||
[[Image:Principle of HaloTag.jpg]] | |||
==== Mechanism ==== | ==== Mechanism ==== | ||
Revision as of 04:35, 30 November 2025
APhotoswitchable HaloTag for Spatiotemporal Control of Fluorescence in Living Cells
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