9MUU
Oxidized state of a turn-off thiol-disulfide redox biosensor with a fluorescence-lifetime readout
Summary for 9MUU
| Entry DOI | 10.2210/pdb9muu/pdb |
| Descriptor | Fluorescent thiol-disulfide redox biosensor, ACETATE ION, FORMIC ACID, ... (5 entities in total) |
| Functional Keywords | fluorescence lifetime, thiol-disulfide redox, fluorescent protein |
| Biological source | Aequorea victoria |
| Total number of polymer chains | 3 |
| Total formula weight | 85992.87 |
| Authors | |
| Primary citation | Rosen, P.C.,Glaser, A.,Martinez-Francois, J.R.,Lim, D.C.,Brooks, D.J.,Fu, P.,Kim, E.,Kern, D.,Yellen, G. Mechanism and application of thiol-disulfide redox biosensors with a fluorescence-lifetime readout. Proc.Natl.Acad.Sci.USA, 122:e2503978122-e2503978122, 2025 Cited by PubMed Abstract: Genetically encoded biosensors with changes in fluorescence lifetime (as opposed to fluorescence intensity) can quantify small molecules in complex contexts, even in vivo. However, lifetime-readout sensors are poorly understood at a molecular level, complicating their development. Although there are many sensors that have fluorescence-intensity changes, there are currently only a few with fluorescence-lifetime changes. Here, we optimized two biosensors for thiol-disulfide redox (RoTq-Off and RoTq-On) with opposite changes in fluorescence lifetime in response to oxidation. Using biophysical approaches, we showed that the high-lifetime states of these sensors lock the chromophore more firmly in place than their low-lifetime states do. Two-photon fluorescence lifetime imaging of RoTq-On fused to a glutaredoxin (Grx1) enabled robust, straightforward monitoring of cytosolic glutathione redox state in acute mouse brain slices. The motional mechanism described here is probably common and may inform the design of other lifetime-readout sensors; the Grx1-RoTq-On fusion sensor will be useful for studying glutathione redox in physiology. PubMed: 40327692DOI: 10.1073/pnas.2503978122 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.15 Å) |
Structure validation
Download full validation report






