Redox-Responsive Fluorescent Probes with Different Design Strategies.

In an aerobic organism, reactive oxygen species (ROS) are an inevitable metabolic byproduct. Endogenously produced ROS have a significant role in physiological processes, but excess ROS can cause oxidative stress and can damage tissue. Cells possess elaborate mechanisms to regulate their internal redox status. The intracellular redox homeostasis plays an essential role in maintaining cellular function. However, moderate alterations in redox balance can accompany major transitions in a cell's life cycle. Because of the role of ROS in physiology and in pathology, researchers need new tools to study redox chemistry in biological systems.In recent years, researchers have made remarkable progress in developing new, highly sensitive and selective fluorescent probes that respond to redox changes, and in this Account we highlight related research, primarily from our own group. We present an overview of the design, photophysical properties, and fluorescence transduction mechanisms of reported molecules that probe redox changes. We have designed and synthesized a series of fluorescent probes for redox cycles in biological systems relying on the active center of glutathione peroxidase (GPx). We have also constructed probes based on the oxidation and reduction of hydroquinone and of 2,2,6,6-tetramethylpiperidinooxy (TEMPO). Most of these probes exhibit high sensitivity and good selectivity, absorb in the near-infrared, and respond rapidly. Such probes are useful for confocal fluorescence microscopy, a dynamic imaging technique that could allow researchers to observe biologically important ROS and antioxidants in real time. This technique and these probes provide potentially useful tools for exploring the generation, transport, physiological function, and pathogenic mechanisms of ROS and antioxidants.We also describe features that could improve the properties of redox-responsive fluorescent probes: greater photostability; rapid, dynamic, cyclic and ratiometric responses; and broader absorption in the near-IR region. In addition, fluorescent probes that include organochalcogens such as selenium and tellurium show promise for a new class of fluorescent redox probes that are both chemically stable and robustly reversible. However, further investigations of the chemical and fluorescence transduction mechanisms of selenium-based probes in response to ROS are needed.

[1]  Evan W. Miller,et al.  A fluorescent sensor for imaging reversible redox cycles in living cells. , 2007, Journal of the American Chemical Society.

[2]  C. Filesi,et al.  Novel mechanisms of natural antioxidant compounds in biological systems: involvement of glutathione and glutathione-related enzymes. , 2005, The Journal of nutritional biochemistry.

[3]  S. Bottle,et al.  Two-Photon Fluorescence Microscopy Imaging of Cellular Oxidative Stress Using Profluorescent Nitroxides , 2012, Journal of the American Chemical Society.

[4]  R. Krämer,et al.  A fluorescent redox sensor with tuneable oxidation potential. , 2010, Bioorganic & medicinal chemistry letters.

[5]  M. Toledano,et al.  ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis , 2007, Nature Reviews Molecular Cell Biology.

[6]  G. He,et al.  Solvent effects on 3-keto-1H-pyrido[3,2,1-kl]phenothiazine fluorescence in polar and protic solvents. , 2011, The journal of physical chemistry. B.

[7]  Guang-Yue Li,et al.  TD‐DFT study on the sensing mechanism of a fluorescent chemosensor for fluoride: Excited‐state proton transfer , 2010, J. Comput. Chem..

[8]  Nam Sang Cheung,et al.  Chlorinative stress: an under appreciated mediator of neurodegeneration? , 2007, Cellular signalling.

[9]  B. Tang,et al.  A near-infrared reversible fluorescent probe for peroxynitrite and imaging of redox cycles in living cells. , 2011, Chemical communications.

[10]  Tymish Y. Ohulchanskyy,et al.  Organotellurium Fluorescence Probes for Redox Reactions: 9-Aryl-3,6-diaminotelluroxanthylium Dyes and Their Telluroxides , 2013 .

[11]  Shaomin Ji,et al.  A highly selective red-emitting FRET fluorescent molecular probe derived from BODIPY for the detection of cysteine and homocysteine: an experimental and theoretical study , 2012 .

[12]  Bryan C Dickinson,et al.  Mitochondrial-targeted fluorescent probes for reactive oxygen species. , 2010, Current opinion in chemical biology.

[13]  A. Kettle,et al.  Inside the neutrophil phagosome: oxidants, myeloperoxidase, and bacterial killing. , 1998, Blood.

[14]  W. Pryor,et al.  Peroxynitrite, a cloaked oxidant formed by nitric oxide and superoxide. , 1992, Chemical research in toxicology.

[15]  P. Li,et al.  A reversible fluorescent probe for detecting hypochloric acid in living cells and animals: utilizing a novel strategy for effectively modulating the fluorescence of selenide and selenoxide. , 2013, Chemical communications.

[16]  Peng Li,et al.  Reversible near-infrared fluorescent probe introducing tellurium to mimetic glutathione peroxidase for monitoring the redox cycles between peroxynitrite and glutathione in vivo. , 2013, Journal of the American Chemical Society.

[17]  S. Gibson,et al.  Chalcogenapyrylium dyes as photochemotherapeutic agents. 2. Tumor uptake, mitochondrial targeting, and singlet-oxygen-induced inhibition of cytochrome c oxidase. , 1990, Journal of medicinal chemistry.

[18]  Long Yi,et al.  A highly sensitive fluorescence probe for fast thiol-quantification assay of glutathione reductase. , 2009, Angewandte Chemie.

[19]  Tianshu Chu,et al.  TD-DFT study on the excited-state proton transfer in the fluoride sensing of a turn-off type fluorescent chemosensor based on anthracene derivatives. , 2012, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.

[20]  M. Davies,et al.  Selenium-containing amino acids are targets for myeloperoxidase-derived hypothiocyanous acid: determination of absolute rate constants and implications for biological damage , 2011, The Biochemical journal.

[21]  Harkesh B. Singh,et al.  Synthesis, structure, and glutathione peroxidase-like activity of amino acid containing ebselen analogues and diaryl diselenides. , 2011, Chemistry.

[22]  Timothy R. Cook,et al.  Photophysical properties of self-assembled multinuclear platinum metallacycles with different conformational geometries. , 2013, Journal of the American Chemical Society.

[23]  H. Sies,et al.  Chemistry of biologically important synthetic organoselenium compounds. , 2001, Chemical reviews.

[24]  J. Schneider,et al.  De novo designed peptidic redox potential probe: linking sensitized emission to disulfide bond formation. , 2004, Journal of the American Chemical Society.

[25]  L. Liaudet,et al.  Nitric oxide and peroxynitrite in health and disease. , 2007, Physiological reviews.

[26]  Y. Urano,et al.  A reversible near-infrared fluorescence probe for reactive oxygen species based on Te-rhodamine. , 2012, Chemical communications.

[27]  Wei Feng,et al.  Luminescent chemodosimeters for bioimaging. , 2013, Chemical reviews.

[28]  D. Churchill,et al.  Selenium- and tellurium-containing fluorescent molecular probes for the detection of biologically important analytes. , 2014, Accounts of chemical research.

[29]  J. McCord,et al.  Oxygen-derived free radicals in postischemic tissue injury. , 1985, The New England journal of medicine.

[30]  D. Leibfritz,et al.  Free radicals and antioxidants in normal physiological functions and human disease. , 2007, The international journal of biochemistry & cell biology.

[31]  Huimin Ma,et al.  Design strategies for water-soluble small molecular chromogenic and fluorogenic probes. , 2014, Chemical reviews.

[32]  G. Milligan,et al.  Real-time monitoring of redox changes in the mammalian endoplasmic reticulum , 2011, Journal of Cell Science.

[33]  Peng Li,et al.  Development of a selenide-based fluorescent probe for imaging hypochlorous acid in lysosomes , 2015 .

[34]  Fabiao Yu,et al.  Development of reversible fluorescence probes based on redox oxoammonium cation for hypobromous acid detection in living cells. , 2012, Chemical communications.

[35]  W. Koppenol,et al.  Selenium and sulfur in exchange reactions: a comparative study. , 2010, The Journal of organic chemistry.

[36]  D. Churchill,et al.  Facile meso-BODIPY annulation and selective sensing of hypochlorite in water. , 2014, Organic letters.

[37]  N. Vermeulen,et al.  Biomarkers of free radical damage applications in experimental animals and in humans. , 1999, Free radical biology & medicine.

[38]  Keli Han,et al.  The invalidity of the photo-induced electron transfer mechanism for fluorescein derivatives. , 2012, Physical chemistry chemical physics : PCCP.

[39]  S. Arai,et al.  A TEMPO-conjugated fluorescent probe for monitoring mitochondrial redox reactions. , 2012, Chemical communications.

[40]  R. Tsien,et al.  Imaging Dynamic Redox Changes in Mammalian Cells with Green Fluorescent Protein Indicators* , 2004, Journal of Biological Chemistry.

[41]  Leland L Smith,et al.  Oxygen, oxysterols, ouabain, and ozone: a cautionary tale. , 2004, Free radical biology & medicine.

[42]  F. Nome,et al.  GPx-Like activity of selenides and selenoxides: experimental evidence for the involvement of hydroxy perhydroxy selenane as the active species. , 2012, Journal of the American Chemical Society.

[43]  Keli Han,et al.  Mechanisms of ultrafast fluorescence depletion spectroscopy and applications to measure slovation dynamics of coummarin 153 in methanol , 2012 .

[44]  P. Li,et al.  A fluorescent probe for rapid detection of thiols and imaging of thiols reducing repair and H2O2 oxidative stress cycles in living cells. , 2013, Chemical communications.

[45]  Guoyao Wu,et al.  Free radicals, antioxidants, and nutrition. , 2002, Nutrition.

[46]  W. Dröge Free radicals in the physiological control of cell function. , 2002, Physiological reviews.

[47]  A Wendel,et al.  The refined structure of the selenoenzyme glutathione peroxidase at 0.2-nm resolution. , 1983, European journal of biochemistry.

[48]  Tianshu Chu,et al.  TD-DFT study on fluoride-sensing mechanism of 2-(2'-phenylureaphenyl)benzoxazole: the way to inhibit the ESIPT process. , 2011, Physical chemistry chemical physics : PCCP.

[49]  Guang-Yue Li,et al.  A TD‐DFT study on the cyanide‐chemosensing mechanism of 8‐formyl‐7‐hydroxycoumarin , 2011, J. Comput. Chem..

[50]  Tymish Y. Ohulchanskyy,et al.  Synthesis and Properties of Heavy Chalcogen Analogues of the Texas Reds and Related Rhodamines , 2014, Organometallics.

[51]  H. Maeda,et al.  2,4-Dinitrobenzenesulfonyl fluoresceins as fluorescent alternatives to Ellman's reagent in thiol-quantification enzyme assays. , 2005, Angewandte Chemie.

[52]  C. Jacob,et al.  Tellurium: an element with great biological potency and potential. , 2010, Organic & biomolecular chemistry.

[53]  Peng Li,et al.  A near-infrared reversible and ratiometric fluorescent probe based on Se-BODIPY for the redox cycle mediated by hypobromous acid and hydrogen sulfide in living cells. , 2013, Chemical communications.

[54]  Keli Han,et al.  Hydrogen bonding in the electronic excited state. , 2012, Accounts of chemical research.

[55]  Keli Han,et al.  A reversible fluorescence probe based on Se-BODIPY for the redox cycle between HClO oxidative stress and H2S repair in living cells. , 2013, Chemical communications.

[56]  F. Meyskens,et al.  UC Irvine UC Irvine Previously Published Works Title Reactive oxygen species : a breath of life or death ? , 2007 .

[57]  K. P. Bhabak,et al.  Functional mimics of glutathione peroxidase: bioinspired synthetic antioxidants. , 2010, Accounts of chemical research.

[58]  M. Jonsson,et al.  The antioxidant profile of 2,3-dihydrobenzo[b]furan-5-ol and its 1-thio, 1-seleno, and 1-telluro analogues. , 2001, Journal of the American Chemical Society.

[59]  Andreas J Meyer,et al.  Real-time imaging of the intracellular glutathione redox potential , 2008, Nature Methods.

[60]  Harkesh B. Singh,et al.  Glutathione peroxidase-like antioxidant activity of diaryl diselenides: a mechanistic study. , 2001, Journal of the American Chemical Society.

[61]  Juyoung Yoon,et al.  Fluorescent and luminescent probes for detection of reactive oxygen and nitrogen species. , 2011, Chemical Society reviews.

[62]  Shaomin Ji,et al.  Highly selective fluorescent OFF-ON thiol probes based on dyads of BODIPY and potent intramolecular electron sink 2,4-dinitrobenzenesulfonyl subunits. , 2011, Organic & biomolecular chemistry.

[63]  P. Zhou,et al.  Experimental and theoretical study on the sensing mechanism of a fluorescence probe for hypochloric acid: a Se···N nonbonding interaction modulated twisting process. , 2014, Physical chemistry chemical physics : PCCP.

[64]  E. Dratz,et al.  Relative reactivity of lysine and other peptide-bound amino acids to oxidation by hypochlorite. , 2000, Free radical biology & medicine.

[65]  W. Heo,et al.  Selective and sensitive superoxide detection with a new diselenide-based molecular probe in living breast cancer cells. , 2014, Organic letters.

[66]  S. Weiss,et al.  Brominating oxidants generated by human eosinophils. , 1986, Science.

[67]  Shu-Pao Wu,et al.  Hypochlorous acid turn-on fluorescent probe based on oxidation of diphenyl selenide. , 2013, Organic letters.

[68]  P. Li,et al.  A near-IR reversible fluorescent probe modulated by selenium for monitoring peroxynitrite and imaging in living cells. , 2011, Journal of the American Chemical Society.

[69]  Jianzhang Zhao,et al.  Facilitative functionalization of cyanine dye by an on-off-on fluorescent switch for imaging of H2O2 oxidative stress and thiols reducing repair in cells and tissues. , 2012, Chemical communications.

[70]  Jean-Pierre Jacquot,et al.  Redox-sensitive GFP in Arabidopsis thaliana is a quantitative biosensor for the redox potential of the cellular glutathione redox buffer. , 2007, The Plant journal : for cell and molecular biology.

[71]  A. Benniston,et al.  Redox‐Controlled Fluorescence Modulation in a BODIPY‐Quinone Dyad , 2008 .

[72]  Elias S. J. Arnér,et al.  Reactive oxygen species, antioxidants, and the mammalian thioredoxin system. , 2001, Free radical biology & medicine.

[73]  Christian Appenzeller‐Herzog Glutathione- and non-glutathione-based oxidant control in the endoplasmic reticulum , 2011, Journal of Cell Science.

[74]  Devin Oglesbee,et al.  Investigating Mitochondrial Redox Potential with Redox-sensitive Green Fluorescent Protein Indicators* , 2004, Journal of Biological Chemistry.