5fhv

Crystal structure of mCherry after reaction with 2-mercaptoethanol

spinqualitylabelsall models 5fhv, resolution 1.55Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 5fhv is a 1 chain structure with sequence from Discosoma sp.. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 1.55Å Ligands: BME, CH6, MCQ, P6G, PGE Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function D0VWW2_DISSP Publication Abstract from PubMed Fluorophores with dynamic or controllable fluorescence emission have become essential tools for advanced imaging, such as superresolution imaging. These applications have driven the continuing development of photoactivatable or photoconvertible labels, including genetically encoded fluorescent proteins. These new probes work well but require the introduction of new labels that may interfere with the proper functioning of existing constructs and therefore require extensive functional characterization. In this work we show that the widely used red fluorescent protein mCherry can be brought to a purely chemically induced blue-fluorescent state by incubation with beta-mercaptoethanol (betaME). The molecules can be recovered to the red fluorescent state by washing out the betaME or through irradiation with violet light, with up to 80% total recovery. We show that this can be used to perform single-molecule localization microscopy (SMLM) on cells expressing mCherry, which renders this approach applicable to a very wide range of existing constructs. We performed a detailed investigation of the mechanism underlying these dynamics, using X-ray crystallography, NMR spectroscopy, and ab initio quantum-mechanical calculations. We find that the betaME-induced fluorescence quenching of mCherry occurs both via the direct addition of betaME to the chromophore and through betaME-mediated reduction of the chromophore. These results not only offer a strategy to expand SMLM imaging to a broad range of available biological models, but also present unique insights into the chemistry and functioning of a highly important class of fluorophores. Efficient switching of mCherry fluorescence using chemical caging.,Cloin BMC, De Zitter E, Salas D, Gielen V, Folkers GE, Mikhaylova M, Bergeler M, Krajnik B, Harvey J, Hoogenraad CC, Van Meervelt L, Dedecker P, Kapitein LC Proc Natl Acad Sci U S A. 2017 Jul 3;114(27):7013-7018. doi:, 10.1073/pnas.1617280114. Epub 2017 Jun 19. PMID:28630286 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See Also Green Fluorescent Protein 3D structures

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