Efficient switching of mCherry fluorescence using chemical caging.

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第一作者： Bas M C,Cloin

第一单位： Cell Biology, Department of Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, The Netherlands.

作者： Bas M C,Cloin ^[1] ; Elke,De Zitter ^[2] ; Desiree,Salas ^[1] ; Vincent,Gielen ^[2] ; Gert E,Folkers ^[3] ; Marina,Mikhaylova ^[1] ; Maike,Bergeler ^[4] ; Bartosz,Krajnik ^[5] ; Jeremy,Harvey ^[4] ; Casper C,Hoogenraad ^[1] ; Luc,Van Meervelt ^[2] ; Peter,Dedecker ^[6] ; Lukas C,Kapitein ^[7]

作者单位： Cell Biology, Department of Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, The Netherlands. ^[1] Biochemistry, Molecular and Structural Biology, Department of Chemistry, KU Leuven, 3001 Heverlee, Belgium. ^[2] NMR Spectroscopy, Department of Chemistry, Faculty of Science, Utrecht University, 3584 CH Utrecht, The Netherlands. ^[3] Quantum Chemistry and Physical Chemistry, Department of Chemistry, KU Leuven, 3001 Heverlee, Belgium. ^[4] Molecular Imaging and Photonics, Department of Chemistry, KU Leuven, 3001 Heverlee, Belgium.;Institute of Physics, Faculty of Physics, Astronomy, and Informatics, Nicolaus Copernicus University, 87-100 Torun, Poland. ^[5] Biochemistry, Molecular and Structural Biology, Department of Chemistry, KU Leuven, 3001 Heverlee, Belgium; l.kapitein@uu.nl peter.dedecker@chem.kuleuven.be. ^[6] Cell Biology, Department of Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, The Netherlands; l.kapitein@uu.nl peter.dedecker@chem.kuleuven.be. ^[7]

关键词 fluorescent proteins localization microscopy mCherry photoactivation β-mercaptoethanol