A red-shifted two-photon-only caging group for three-dimensional photorelease† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc05182d
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Andreas Dreuw | Alexander Heckel | A. Dreuw | P. Walla | A. Heckel | J. Wachtveitl | Josef Wachtveitl | Yvonne Becker | Erik Unger | Manuela A H Fichte | Daniel A Gacek | Peter J Walla | Yvonne Becker | M. Fichte | D. A. Gacek | E. Unger
[1] T. M. Dore,et al. Substituent effects on the sensitivity of a quinoline photoremovable protecting group to one- and two-photon excitation. , 2009, The Journal of organic chemistry.
[2] Laura N. Vandenberg,et al. Light-activated serotonin for exploring its action in biological systems. , 2013, Chemistry & biology.
[3] A. Heckel,et al. Three-Dimensional Control of DNA Hybridization by Orthogonal Two-Color Two-Photon Uncaging. , 2016, Angewandte Chemie.
[4] Cloaked Caged Compounds: Chemical Probes for Two-Photon Optoneurobiology. , 2017, Angewandte Chemie.
[5] A. Heckel,et al. Light-controlled tools. , 2012, Angewandte Chemie.
[6] C. Bochet,et al. New safety-catch photolabile protecting group. , 2007, Organic letters.
[7] S. Dimmeler,et al. Light-inducible antimiR-92a as a therapeutic strategy to promote skin repair in healing-impaired diabetic mice , 2017, Nature Communications.
[8] P. Lipp,et al. Fundamental calcium release events revealed by two‐photon excitation photolysis of caged calcium in guinea‐pig cardiac myocytes , 1998, The Journal of physiology.
[9] S. Tretiak,et al. Enhanced Two‐Photon Absorption of Organic Chromophores: Theoretical and Experimental Assessments , 2008 .
[10] Yi Luo,et al. Simulations of vibronic profiles in two-photon absorption , 2000 .
[11] G. Ellis‐Davies,et al. The nitrodibenzofuran chromophore: a new caging group for ultra-efficient photolysis in living cells , 2005, Nature Methods.
[12] Hai Qi,et al. Total chemical synthesis of photoactivatable proteins for light-controlled manipulation of antigen–antibody interactions , 2015, Chemical science.
[13] D. Lawrence,et al. Spatially discrete, light-driven protein expression. , 2002, Chemistry & biology.
[14] P. Neveu,et al. o-nitrobenzyl photolabile protecting groups with red-shifted absorption: syntheses and uncaging cross-sections for one- and two-photon excitation. , 2006, Chemistry.
[15] Alexander Deiters,et al. Optical Control of CRISPR/Cas9 Gene Editing. , 2015, Journal of the American Chemical Society.
[16] Andreas Dreuw,et al. Computational design of improved two‐photon active caging compounds based on nitrodibenzofuran , 2012, J. Comput. Chem..
[17] T. Moore,et al. Two-Photon Spectra of Chlorophylls and Carotenoid-Tetrapyrrole Dyads. , 2017, The journal of physical chemistry. B.
[18] W. Denk,et al. Two-photon scanning photochemical microscopy: mapping ligand-gated ion channel distributions. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[19] L. Vyklický,et al. New caged neurotransmitter analogs selective for glutamate receptor sub-types based on methoxynitroindoline and nitrophenylethoxycarbonyl caging groups , 2012, Neuropharmacology.
[20] Maria Goeppert-Mayer. Über Elementarakte mit zwei Quantensprüngen , 1931 .
[21] Laura A. Sordillo,et al. Transmission in near‐infrared optical windows for deep brain imaging , 2016, Journal of biophotonics.
[22] Kira E. Poskanzer,et al. A Visible-Light-Sensitive Caged Serotonin. , 2017, ACS chemical neuroscience.
[23] C. Katan,et al. Design and Synthesis of Two-Photon Responsive Chromophores for Near-Infrared Light-Induced Uncaging Reactions , 2017, Synthesis.
[24] A. Heckel,et al. Four levels of wavelength-selective uncaging for oligonucleotides. , 2013, Organic letters.
[25] J. Kaplan,et al. Rapid photolytic release of adenosine 5'-triphosphate from a protected analogue: utilization by the Na:K pump of human red blood cell ghosts. , 1978, Biochemistry.
[26] I. Dmochowski,et al. Oligonucleotide modifications enhance probe stability for single cell transcriptome in vivo analysis (TIVA). , 2017, Organic & biomolecular chemistry.
[27] Verónica San Miguel,et al. Wavelength-selective caged surfaces: how many functional levels are possible? , 2011, Journal of the American Chemical Society.
[28] R. Givens,et al. Photoremovable Protecting Groups in Chemistry and Biology: Reaction Mechanisms and Efficacy , 2012, Chemical reviews.
[29] Federico Guillermo Cruz,et al. Light-Activated Gene Expression , 2000 .
[30] E M Callaway,et al. Brominated 7-hydroxycoumarin-4-ylmethyls: photolabile protecting groups with biologically useful cross-sections for two photon photolysis. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[31] Qiuping Guo,et al. A new class of homogeneous nucleic acid probes based on specific displacement hybridization. , 2002, Nucleic acids research.
[32] D. Piston,et al. The efficiency of two-photon photolysis of a "caged" fluorophore, o-1-(2-nitrophenyl)ethylpyranine, in relation to photodamage of synaptic terminals , 2002, European Biophysics Journal.
[33] W. Denk,et al. Two-photon laser scanning fluorescence microscopy. , 1990, Science.