RATIOMETRIC NEAR-INFRARED FLUORESCENT PROBES FOR THE SENSITIVE DETECTION OF INTRACELLULAR PH AND BIO-THIOLS IN LIVE CELLS

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Book Synopsis RATIOMETRIC NEAR-INFRARED FLUORESCENT PROBES FOR THE SENSITIVE DETECTION OF INTRACELLULAR PH AND BIO-THIOLS IN LIVE CELLS by :

Download or read book RATIOMETRIC NEAR-INFRARED FLUORESCENT PROBES FOR THE SENSITIVE DETECTION OF INTRACELLULAR PH AND BIO-THIOLS IN LIVE CELLS written by and published by . This book was released on 2020 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract : In the past twenty years, fluorescence sensing and imaging based on fluorescent probes has been developed as an imperative technique due to the merits including excellent sensitivity, operational simplicity, instant time effectiveness and outstanding selectivity in the research areas such as mineralogy, gemology, biological medicine, materials and environmental engineering. Protons act as a significant role in a variety of pathological and physiological processes, and there are obvious differences in the pH among organelles: the pH in lysosomes is acid within the range of 4.5-5.5, whereas mitochondrial pH is basic that can be as high as 8.0. Abnormal intracellular pH is always an indication of a disrupted pH homeostasis in the whole cell. Furthermore, intracellular bio-thiols are vital to cell metabolism, which by either elevated or deficiency levels of bio-thiols will lead to some diseases. Possessing the advantages of avoiding systematic errors and undesirable photophysical properties of certain fluorophores, novel near-infrared ratiometric fluorescent sensors for the accurately monitoring intracellular pH and biothiols have become the spotlight in research topics. Throughout this dissertation, we firstly have designed and synthesized two novel rhodamine-based dyes with high fluorescence quantum yield, good pH stability large Stokes shifts and excellent photostability by introducing an additional amino residue with fused rings into a classic rhodamine skeleton. We also have constructed a fluorescent sensor by incorporating a receptor to one of these dyes and applied it as an effective sensor for the quick and sensitive monitoring of lysosomal pH fluctuations. Then, we have prepared two sets of ratiometric fluorescent probes for the sensitive detection of lysosomal pH values. The former series were based on π-conjugation modulation strategy, which was accomplished by conjugating a visible coumarin motif to a classic near-infrared hemicyanine skeleton via a vinyl linker. The lysosome-targeting goal was reached by introducing a morpholine ligand or a o-phenylenediamine group to the hemicyanine acceptor. For the latter series, we have obtained three near-infrared ratiometric fluorescent sensors containing a TPE as a donor and a rhodamine as an acceptor for the quantitative, sensitive and comparative analysis of lysosomal pH alterations through FRET and TBET approaches. Furthermore, we have prepared two near-infrared hybrid rhodol dyes for the ratiometric and sensitive visualization of pH value alterations in mitochondria taking advantage of conjugating typical hemicyanine fluorophores into a classic rhodol motif. Upon pH changes, a rhodol hydroxyl group in the probe acts as a spiropyran switch, resulting in the change of π-conjugation and the appearance of a new fluorescent peak. Due to the positive charge, these two novel rhodol dyes possessed the mitochondria-targeting property. In the end, besides the ratiometric fluorescent pH probes, we have reported a FRET-based fluorescent sensor for the ratiometric, selective and accurate detection of cysteine (Cys), which was achieved by linking a visible coumarin skeleton and a near-infrared rhodamine motif through a piperazine spacer. This probe could be used to monitor the intracellular cysteine concentration ratiometrically and be further applied for imaging of Drosophila melanogaster larvae to detect cysteine concentration alterations in vivo.

NEAR-INFRARED FLUORESCENT PROBES FOR SENSITIVE DETERMINATION OF LYSOSOMAL & MITOCHONDRIAL PH IN LIVE CELLS

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ISBN 13 :
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Book Synopsis NEAR-INFRARED FLUORESCENT PROBES FOR SENSITIVE DETERMINATION OF LYSOSOMAL & MITOCHONDRIAL PH IN LIVE CELLS by :

Download or read book NEAR-INFRARED FLUORESCENT PROBES FOR SENSITIVE DETERMINATION OF LYSOSOMAL & MITOCHONDRIAL PH IN LIVE CELLS written by and published by . This book was released on 2019 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract : Varied intracellular pH levels are critical for various physiological processes such as enzymatic activity, cell proliferation and apoptosis, ion transport, and muscle contraction. Cellular compartments, like lysosomes, must retain an acidic environment (pH ~ 4.5) to activate hydrolytic enzymes necessary for the breakdown of large biomolecules. Another cellular organelle, the mitochondria, provides the cell with energy and must retain an alkalis environment (pH ~ 8.0) for proper function. Substantial lysosomal and mitochondrial pH deviation is associated with cellular dysfunction and disease. Therefore, the precise detection of lysosomal and mitochondrial pH is essential to provide a better understanding of cellular physiological and pathological processes. Due to their superior features, such as cheap and simple operation, high spatial and temporal resolution, and noninvasive fluorescence imaging, fluorescent probes are the ideal methodology to visualize and monitor lysosomal and mitochondrial pH variation. We have developed three morpholine-functionalized BODIPY-based fluorescent probes that can be used to monitor lysosomal pH. The fluorescent probes are highly fluorescent under basic conditions, but when exposed to an acidic environment the fluorescence is quenched via an electron donor photoinduced energy transfer. Moreover, we have developed and synthesized a series of sterically hindered fluorescent probes based on spirolactam ring modifications. These modifications were developed by introducing 2-aminophenylboronic acid pinacol ester to rhodamine B, a near-infrared rhodamine dye, and a near-infrared hemicyanine dye. The probes display high fluorescence under acidic conditions but exhibit weak fluorescence under basic conditions due to the significant steric hindrance in the spirolactam ring. Since the probes were functional in an acidic environment, they were successfully applied for the sensing of lysosomal pH variations in living cells. We have also developed a NIR fluorescent probe to determine mitochondrial pH variations by incorporating an oxazolidine switch onto a near-infrared hemicyanine. The probe has the ability to rapidly switch from an oxazolidine moiety to a hemicyanine group when the pH level decreases from 10.0 to 5.0. This response to pH changes is reversible and has been successfully used to determine pH levels in mitochondria.

DESIGN AND DEVELOPMENT OF NEAR-INFRARED FLUORESCENT PROBES FOR SENSING PH, HYPOXIA AND PEROXYNITRITE

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ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (126 download)

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Book Synopsis DESIGN AND DEVELOPMENT OF NEAR-INFRARED FLUORESCENT PROBES FOR SENSING PH, HYPOXIA AND PEROXYNITRITE by :

Download or read book DESIGN AND DEVELOPMENT OF NEAR-INFRARED FLUORESCENT PROBES FOR SENSING PH, HYPOXIA AND PEROXYNITRITE written by and published by . This book was released on 2021 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract : pH and hypoxia levels are two important diagnostic biomarkers in biological systems and abnormal levels will cause many diseases. The metabolism and transportation of peroxynitrite in biological systems involve a series of important enzymes and proteins. Peroxynitrite generation represents a crucial pathogenic mechanism in conditions such as stroke, myocardial infarction, chronic heart failure, diabetes, circulatory shock, chronic inflammatory diseases, cancer, and neurodegenerative disorders. As a result, it is very important to detect and evaluate the levels of pH, hypoxia, and peroxynitrite in vivo to study the functionality of enzymes and provide practical applications for cancer diagnosis and therapy. Fluorescence detection and imaging offer a sensitive non-invasive method because it provides clear images of cellular three-dimensional structures, and can illustrate cellular multiple overlapping structures simultaneously, and enable image-guided surgery. However, it is challenging to design fluorescent probes with good fluorescence signals, low background noise, and multifunctional detection capability. In order to overcome these drawbacks, we have designed and synthesized a series of excellent fluorescent probes to detect pH, hypoxia, and peroxynitrite with good fluorescence signals, fast responses, low background noise, and multifunctional detection capabilities. The probes combine advantages of near-infrared imaging such as low fluorescence background interference, less photodamage to cells and tissues, and deep-tissue penetration with ratiometric imaging, this latter aspect reduces systematic errors with solely intensity-based fluorescent probes caused by fluctuations in the excitation light source, variations in probe concentrations, and different probe compartmental localizations. We have developed a new backbone for making near-infrared fluorescent probes. This new backbone has a reactive chlorine group for modifying the detectors. Based on this new backbone, we introduced a pH-responsive detector to prepare three pH-sensitive near-infrared fluorescent probes with high fluorescence quantum yields. We designed and synthesized a series of fluorescent probes on detecting hypoxia level. The nitro group was introduced directly in the conjugation system of the fluorophore, which make it fast response and ultra-sensitive. Additionally, by changing the electron-withdrawing abilities of the substitution group on 9-position of acridine moiety, the fluorescent probes show a significant different detection limit and sensitivity towards nitroreducatse. For third project, we developed a fluorescent probe responding to peroxynitrite. The probe contains a near-infrared fluorophore and a coumarin moiety and connected through a conjugated triple bond linker. The ester group of the coumarin moiety in the conjugation system can enhance the sensitivity of the ONOO- detection. For the fourth project, we developed multi-response fluorescent probe. This probe can detect pH and ONOO- with different fluorescent changes. Base pH condition can induce an on-off fluorescent change on the probe, and the ONOO- can generate a ratiometric fluorescent change.

NOVEL FLUORESCENT PROBES FOR VISUALIZATION OF PH CHANGES AND Zn (II) IONS IN LIVE CELLS

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ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (115 download)

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Book Synopsis NOVEL FLUORESCENT PROBES FOR VISUALIZATION OF PH CHANGES AND Zn (II) IONS IN LIVE CELLS by :

Download or read book NOVEL FLUORESCENT PROBES FOR VISUALIZATION OF PH CHANGES AND Zn (II) IONS IN LIVE CELLS written by and published by . This book was released on 2018 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract : Intracellular pH plays many significant roles in various cellular processes including cell proliferation, cell growth, apoptosis, signal transduction, and cellular metabolism. Lysosome is a membrane-bound organelle with pH 4.5-5.0 which is found in virtually all animal cells. Zn (II) ions extensively exist in human cells and body fluid. Research revealed that Zn (II) ions involved in many metabolism process such as cell growth, reproduction, and tissue regeneration. Near-infrared (NIR) fluorescent probes for the detection of intracellular pH and Zn (II) ions have become hot research topics because of the advantages of high sensitivity, easy operation, deep tissues penetration, real-time monitoring, and low background interference. In this dissertation, we reported two NIR fluorescent probes for sensing of intracellular Zn (II) ions. The probes show advantages of large Stokes shift, excellent photostability and good selectivity to Zn (II) over other metal ions. We also developed five coumarin-hybridized near-infrared fluorescent probes for sensing of lysosomal pH changes in both NIR and visible regions. We significantly improved compatibility and water-solubility of the probes by introducing oligo(ethylene glycol) to the fluorophores. In order to overcome fluorescence quenching issue of cyanine dye (IR-780) in aqueous solution, we successfully developed a fluorescent cassette by introducing tetraphenylethene (TPE) derivative to dye IR-780 through an ether bond connection. Both TPE donor and cyanine acceptor in the cassette show significant fluorescence enhancement when the fluorescent cassette becomes aggregated in aqueous solutions. The fluorescent cassette has been used to detect intracellular pH changes in live cells through manipulation of the cassette aggregation status by pH changes. In order to overcome systematic errors of intensity-based fluorescent probes, we also developed three ratiometric fluorescent probes based on BODIPY donors and near-infrared rhodamine or hemicyanine acceptors through electric wire pi-conjugation connections in a through-bond energy transfer approach The probes display ratiometric fluorescence responses to pH decreases from 7.4 to 2.4 with fluorescence decreases of BODIPY donors and fluorescence increases of rhodamine or hemicyanine acceptors.

DEVELOPMENT OF NEAR-INFRARED FLUORESCENT PROBES FOR MONITORING LYSOSOMAL PH CHANGES

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ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (114 download)

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Book Synopsis DEVELOPMENT OF NEAR-INFRARED FLUORESCENT PROBES FOR MONITORING LYSOSOMAL PH CHANGES by :

Download or read book DEVELOPMENT OF NEAR-INFRARED FLUORESCENT PROBES FOR MONITORING LYSOSOMAL PH CHANGES written by and published by . This book was released on 2018 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract : Lysosome is an acidic membrane-bound organelle containing more than 70 hydrolytic enzymes that breaks down different biological macromolecules. Substantial lysosomal pH disruption can cause lysosome malfunction and consequently lead to lysosomal storage disease. Therefore, it is essential to precisely monitor lysosomal pH changes in order to explore cellular functions and get insightful understanding of physiological and pathological processes. Fluorescence imaging based on fluorescent probes is a powerful technique to monitor lysosomal pH changes because of advantageous features including operational simplicity, high sensitivity, non-invasive approach, and high spatial resolution. However, most of the reported lysosomal pH probes are based on Stokes-shift fluorescence with lower energy emission under higher energy excitation, and exhibit less than 600 nm absorption and emission wavelengths, which causes cellular and tissue photodamage and contains biological fluorescence background. In order to avoid these issues, we developed near-infrared fluorescent probes based on single-photon anti-Stokes fluorescence with near-infrared excitations and emissions. We significantly improved biocompatibility and water-solubility of fluorescent probes by introducing mannose residues to the fluorophores through oligo(ethylene glycol) tethered spacers for sensitive detection of lysosomal pH changes in two near-infrared channels. In order to take advantage of ratiometric and near-infrared imaging to overcome systematic errors of intensity-based fluorescent probes caused by probe concentration variation and uneven distribution, temperature, solvent polarity, and excitation light fluctuation, we developed ratiometric near-infrared fluorescent probes for ratiometric detection of lysosomal pH changes by introducing tetraphenylethene (TPE) dyes to hemicyanine dyes. Gradual lysosomal pH decreases result in gradual increases of hemicyanine fluorescence, and corresponding concomitant decreases of TPE fluorescence. The probes allow for development of various ratiometric near-infrared fluorescent probes for quantitative and comparative reliable analyses of cations, reactive nitrogen, oxygen and sulfur species by conjugating various biosensing groups into the near-infrared hemicyanine moieties.

NEAR-INFRARED WATER-SOLUBLE FLUORESCENT PROBES FOR THE DETECTION OF LYSOSOMAL PH AND Zn (II) IONS

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ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (113 download)

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Book Synopsis NEAR-INFRARED WATER-SOLUBLE FLUORESCENT PROBES FOR THE DETECTION OF LYSOSOMAL PH AND Zn (II) IONS by :

Download or read book NEAR-INFRARED WATER-SOLUBLE FLUORESCENT PROBES FOR THE DETECTION OF LYSOSOMAL PH AND Zn (II) IONS written by and published by . This book was released on 2016 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Abstract : Fluorescent probes have become a powerful tool for scientists to selectively detect a wide variety of substances in living cells due to their simplicity and high sensitivity, enabling scientists to monitor them and to understand their physiological and pathological processes. A constant lysosomal pH is a prerequisite for more than 70 kinds of hydrolytic enzymes in lysosomes from all eukaryotic cells to function well, while zinc (II) ions play a vital role in numerous cellular metabolism. Abnormal lysosomal pH and Zn (II) ions concentration in cells always associate with many serious diseases. However, the emission and excitation peak of the most fluorescent probes are in the visible range which cause some issues, such as photo damage to cells and high fluorescence background. Therefore, novel near-infrared fluorescent probes for selectively detecting lysosomal pH and Zn (II) ions, respectively, with good aqueous solubility were developed to overcome these limitations.

A Sensitive Two-photon Ratiometric Fluorescent Probe for Γ-glutamyltranspeptidase Activity Detection and Imaging in Living Cells and Cancer Tissues1

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ISBN 13 :
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Book Rating : 4.:/5 (15 download)

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Book Synopsis A Sensitive Two-photon Ratiometric Fluorescent Probe for Γ-glutamyltranspeptidase Activity Detection and Imaging in Living Cells and Cancer Tissues1 by :

Download or read book A Sensitive Two-photon Ratiometric Fluorescent Probe for Γ-glutamyltranspeptidase Activity Detection and Imaging in Living Cells and Cancer Tissues1 written by and published by . This book was released on 2018 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Near-Infrared Applications in Biotechnology

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Publisher : CRC Press
ISBN 13 : 9781420030242
Total Pages : 408 pages
Book Rating : 4.0/5 (32 download)

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Book Synopsis Near-Infrared Applications in Biotechnology by : Ramesh Raghavachari

Download or read book Near-Infrared Applications in Biotechnology written by Ramesh Raghavachari and published by CRC Press. This book was released on 2020-06-16 with total page 408 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume explores developments in techniques in diagnostics, DNA sequencing, bioanalysis of immunoassays, and single-molecule detection. It promotes the measurement, identification, monitoring, analysis, and application of near-infrared spectroscopy (NIR) to medical and pharmaceutical advances. The text also considers noninvasive methods of NIR for successful, cost-effective, and prompt diagnoses of diseases.

New Chemical Tools for Fluorescent Detection of Hydrogen Peroxide in Living Cells

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ISBN 13 :
Total Pages : 560 pages
Book Rating : 4.:/5 (785 download)

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Book Synopsis New Chemical Tools for Fluorescent Detection of Hydrogen Peroxide in Living Cells by : Duangkhae Srikun

Download or read book New Chemical Tools for Fluorescent Detection of Hydrogen Peroxide in Living Cells written by Duangkhae Srikun and published by . This book was released on 2011 with total page 560 pages. Available in PDF, EPUB and Kindle. Book excerpt: As one of the toxic by-product of aerobic metabolism, hydrogen peroxide (H2O2), at uncontrolled levels and distributions, is a sign of oxidative stress, aging and disease. However, H2O2 also plays an essential part in normal physiological system. H2O2 levels are regulated by many enzymes and metabolites that generate or break-down H2O2. In macrophages, the presence of invading pathogens activates the production of microbicidal levels of H2O2 by NADPH oxidase (Nox). Isoforms of Nox are expressed in many non-phagocytic cells and tissues. Nox-generated H2O2 is a secondary messenger involved in signaling for growth, proliferation, differentiation and controlled cell death; these variations in downstream biological effects are regulated by both the spatial and temporal production of H2O2. Small molecule fluorescent probes bearing boronate ester moieties have been developed for chemoselective detection of H2O2 in both oxidative stress levels and cellular signaling events. This dissertation describes the design, synthesis, characterization and application of new boronate-based fluorescent probes with added functionality. Peroxy-Lucifer-1 (PL1) and Peroxy-Naphthalene-1 (PN1) are ratiometric fluorescent probes that can detect oxidative bursts in immune response events. Ratiometric probes allow simultaneous detection of two signals from the reacted and unreacted probes in the same sample, providing a built-in correction for variations such as uneven probe loading, sample environment and detection efficiency. PN1 also has a high two-photon cross section. The increased penetration depth of near-infrared excitation light allows the detection of H2O2 in tissue specimens with PN1. SNAP-Peroxy-Green-1 (SPG1) and SNAP-Peroxy-Green-2 (SPG2) are capable of detecting local concentration of H2O2 in subcellular compartments such as mitochondria, endoplasmic reticulum, nucleus, and plasma membrane. The precise localization of probes to the targeted organelle is facilitated by highly specific recognition of the SNAP ligand bound to the probe by the SNAP fusion protein. Furthermore, simultaneous detection of H2O2 at two different locations is feasible by using a SNAP tag with an orthogonal CLIP tag; such combined use of SNAP and CLIP tags is assisted by the expanding color palette of SNAP and CLIP peroxy probes. Multi-modal probes using PAMAM-G5 dendrimer platform was developed for the real-time imaging of the interplay between H2O2 and other physiological events. Coordination of the oxidative burst and progressive acidification in phagosomes of macrophages was elucidated with G5-SNARF2-PF1-Ac, a nanoprobe decorated with the H2O2 sensing module PF1 and pH sensor SNARF2.

Fluorescent Energy Transfer Nucleic Acid Probes

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Publisher : Springer Science & Business Media
ISBN 13 : 1597450693
Total Pages : 368 pages
Book Rating : 4.5/5 (974 download)

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Book Synopsis Fluorescent Energy Transfer Nucleic Acid Probes by : Vladimir V. Didenko

Download or read book Fluorescent Energy Transfer Nucleic Acid Probes written by Vladimir V. Didenko and published by Springer Science & Business Media. This book was released on 2008-02-04 with total page 368 pages. Available in PDF, EPUB and Kindle. Book excerpt: Fluorescent nucleic acid probes, which use energy transfer, include such constructs as molecular beacons, molecular break lights, Scorpion primers, TaqMan probes, and others. These probes signal detection of their targets by changing either the intensity or the color of their fluorescence. Not surpr- ingly, these luminous, multicolored probes carry more flashy names than their counterparts in the other fields of molecular biology. In recent years, fluor- cent probes and assays, which make use of energy transfer, have multiplied at a high rate and have found numerous applications. However, in spite of this explosive growth in the field, there are no manuals summarizing different p- tocols and fluorescent probe designs. In view of this, the main objective of Fluorescent Energy Transfer Nucleic Acid Probes: Designs and Protocols is to provide such a collection. Oligonucleotides with one or several chromophore tags can form fluor- cent probes capable of energy transfer. Energy transport within the probe can occur via the resonance energy transfer mechanism, also called Förster tra- fer, or by non-Förster transfer mechanisms. Although the probes using Förster transfer were developed and used first, the later non-Förster-based probes, such as molecular beacons, now represent an attractive and widely used option. The term “fluorescent energy transfer probes” in the title of this book covers both Förster-based fluorescence resonance energy transfer (FRET) probes and probes using non-FRET mechanisms. Energy transfer probes serve as molecule-size sensors, changing their fluorescence upon detection of various DNA reactions.

The Changing Faces of Glutathione, a Cellular Protagonist

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Publisher : Frontiers Media SA
ISBN 13 : 2889195953
Total Pages : 144 pages
Book Rating : 4.8/5 (891 download)

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Book Synopsis The Changing Faces of Glutathione, a Cellular Protagonist by : Alfonso Pompella

Download or read book The Changing Faces of Glutathione, a Cellular Protagonist written by Alfonso Pompella and published by Frontiers Media SA. This book was released on 2015-07-17 with total page 144 pages. Available in PDF, EPUB and Kindle. Book excerpt: Glutathione (GSH) has been described for a long time just as a defensive reagent against the action of toxic xenobiotics (drugs, pollutants, carcinogens), both directly and as a cofactor for GSH transferases. As a prototype antioxidant, it has been involved in cell protection from the noxious effect of excess oxidant stress, both directly and as a cofactor of glutathione peroxidases. In addition, it has long been known that GSH is capable of forming disulfide bonds with cysteine residues of proteins, and the relevance of this mechanism ("S-glutathionylation") in regulation of protein function has been well documented in a number of research fields. Rather paradoxically, it has also been highlighted that GSH—and notably its catabolites, as originated by metabolism by gamma-glutamyltransferase—can promote oxidative processes, by participating in metal ion-mediated reactions eventually leading to formation of reactive oxygen species and free radicals. Also, a fundamental role of GSH has been recognized in the storage and transport of nitric oxide (NO), in the form of S-nitrosoglutathione (GSNO). The significance of GSH as a major factor in regulation of cell life, proliferation, and death, can be regarded as the integrated result of all these roles, as well as of more which are emerging in diverse fields of biology and pathophysiology. Against this background, modulation of GSH levels and GSH-related enzyme activities represents a fertile field for experimental pharmacology in numerous and diverse perspectives of animal, plant and microbiologic research. This research topic includes 14 articles, i.e. 4 Opinion Articles, 6 Reviews, and 4 Original Research Articles. The contributions by several distinguished research groups, each from his own standpoint of competence and expertise, provide a comprehensive and updated view over the diverse roles, the changing faces of GSH and GSH-related enzymes in cell’s health, disease and death.

The Chemistry and Biology of Nitroxyl (HNO)

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Publisher : Elsevier
ISBN 13 : 0128011645
Total Pages : 425 pages
Book Rating : 4.1/5 (28 download)

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Book Synopsis The Chemistry and Biology of Nitroxyl (HNO) by : Fabio Doctorovich

Download or read book The Chemistry and Biology of Nitroxyl (HNO) written by Fabio Doctorovich and published by Elsevier. This book was released on 2016-09-01 with total page 425 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Chemistry and Biology of Nitroxyl (HNO) provides first-of-its-kind coverage of the intriguing biologically active molecule called nitroxyl, or azanone per IUPAC nomenclature, which has been traditionally elusive due to its intrinsically high reactivity. This useful resource provides the scientific basis to understand the chemistry, biology, and technical aspects needed to deal with HNO. Building on two decades of nitric oxide and nitroxyl research, the editors and authors have created an indispensable guide for investigators across a wide variety of areas of chemistry (inorganic, organic, organometallic, biochemistry, physical, and analytical); biology (molecular, cellular, physiological, and enzymology); pharmacy; and medicine. This book begins by exploring the unique molecule’s structure and reactivity, including important reactions with small molecules, thiols, porphyrins, and key proteins, before discussing chemical and biological sources of nitroxyl. Advanced chapters discuss methods for both trapping and detecting nitroxyl by spectroscopy, electrochemistry, and fluorescent inorganic cellular probing. Expanding on the compound’s foundational chemistry, this book then explores its molecular physiology to offer insight into its biological implications, pharmacological effects, and practical issues. Presents the first book on HNO (nitroxyl or azanone), an increasingly important molecule in biochemistry and pharmaceutical research Provides a valuable coverage of HNO’s chemical structure and significant reactions, including practical guidance on working with this highly reactive molecule Contains high quality content from recognized experts in both industry and academia

Fluorescent Probes and Sensors

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Publisher : MDPI
ISBN 13 : 3038429279
Total Pages : 315 pages
Book Rating : 4.0/5 (384 download)

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Book Synopsis Fluorescent Probes and Sensors by : Sheshanath V. Bhosale

Download or read book Fluorescent Probes and Sensors written by Sheshanath V. Bhosale and published by MDPI. This book was released on 2018-05-08 with total page 315 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book is a printed edition of the Special Issue "Fluorescent Probes and Sensors" that was published in Sensors

Design of Novel Biosensors for Optical Sensing and Their Applications in Environmental Analysis

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Publisher : Springer
ISBN 13 : 9811364885
Total Pages : 94 pages
Book Rating : 4.8/5 (113 download)

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Book Synopsis Design of Novel Biosensors for Optical Sensing and Their Applications in Environmental Analysis by : Kun Yin

Download or read book Design of Novel Biosensors for Optical Sensing and Their Applications in Environmental Analysis written by Kun Yin and published by Springer. This book was released on 2019-03-06 with total page 94 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book introduces readers to the development of novel optical biosensors for environmental analysis. Environmental pollution has now become a serious problem, which threatens the health of human beings. Traditional analytical methods have a number of drawbacks, such as the need for professional operators and complicated instruments. After millions of years of evolution, biomolecules can perform various functions with good accuracy and efficiency due to their unique structures, offering a viable alternative to traditional methods. This work focuses on using new biological sensing strategies, e.g. those based on special biomaterials, bio-reactions or living cells, to establish novel biosensors. As these biosensors offer satisfactory optical response performance, they can be used to transform the recognition behavior of specific targets into optical signals and effectively detect target objects.

Fluorescence Probes for Cellular Thiol and Disulfide Detection

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Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (777 download)

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Book Synopsis Fluorescence Probes for Cellular Thiol and Disulfide Detection by : Timothy Jonhera

Download or read book Fluorescence Probes for Cellular Thiol and Disulfide Detection written by Timothy Jonhera and published by . This book was released on 2001 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: The total concentration of cellular thiols is about 30 mM, and use of current fluorescent chemical probes to quantitate these thiols inside cells is impractical. We recently reported fluorescent dithio probes (donor-S-S-acceptor, DSSA) with unusually low reduction potential ( - 0.6 V) that can detect changes in intracellular thiols and cross membranes of bacterial and mammalian cells, but they could not quantify thiol redox state. Here we report a new variant of the DSSA series, which has hydroxy coumarin (Ex: 320 nm, Em: 460 nm) as donor and fluorescein (Ex: 485 nm, Em: 520 nm) as acceptor. The probe was characterized in vitro by titration with glutathione in a physiologically relevant range and monitoring changes in fluorescence emission from both Coumarin and Fluorescein, upon reduction of the disulfide bond that joins this donor-acceptor FRET pair. The ratio of fluorescence emission band intensity, changes upon reduction with glutathione, and because of the probe's low reduction potential, permits quantitative measurement of glutathione levels in the 1 - 10 mM range. This is the first demonstration of ratiometric (FRET-based) thiol level measurement and will be enabling for quantitative assessment of thiol redox state (GSG/GSSG) inside cells. Preliminary studies in E. Coli are also presented. We also report an improved version of our previously reported fluorescent-dithio probes for detecting cellular thiols, referred to as PMR-CYS-FITC, where PMR is p-methyl red (aka dabcyl), a fluorescein quencher. Unlike most thiol-reactive probes, PMR-CYS-FITC can also detect certain disulfides, making it useful for d̀isulfide proteomics'. PMR-CYS-FITC was used to identify new disulfide-containing protein(s) in the zebrafish chorion, with potential role(s) in protecting the embryo during development. Confocal microscopy of the embryo, followed by in-gel staining and imaging of proteins, then tandem MS, led to our discovery of two novel disulfide-containing proteins in the fish chorion, lipovitellin and C-reactive protein (CRP). CRP is a well-known biomarker for infection or inflammation (associated with oxidative stress) in humans, so discovery of CRP in the zebrafish has relevance for its use as a model organism. In vitro biophysical characterization of this probe provides further explanations for the differential reactivity of disulfides, and enhanced fluorescence for some fluorescein-protein mixed disulfides.

Peroxynitrite Detection in Biological Media

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Publisher : Royal Society of Chemistry
ISBN 13 : 1782622357
Total Pages : 251 pages
Book Rating : 4.7/5 (826 download)

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Book Synopsis Peroxynitrite Detection in Biological Media by : Serban Peteu

Download or read book Peroxynitrite Detection in Biological Media written by Serban Peteu and published by Royal Society of Chemistry. This book was released on 2015-10-16 with total page 251 pages. Available in PDF, EPUB and Kindle. Book excerpt: Peroxynitrite is a powerful oxidiser which can damage a wide array of molecules within cells, including DNA and proteins, leading to apoptosis, inflammation or cancer. Peroxynitrite detection and quantification provides critical information in understanding its biological implications. Attempts to investigate the behavior of peroxynitrite in vivo and in vitro have been hampered by the difficulty in detecting this highly reactive oxygen species. This book presents the current state of the art in this research field with contributions from scientific leaders in the field. The chapters make clear the associated challenges and development for selective and sensitive detection of peroxynitrite. This book is a timely addition to the literature, as the first in the field, dedicated to detecting this molecule in vivo. It will be welcomed by the community particularly medicinal and analytical chemists, developers of sensors and probes and analytical equipment manufacturers.

Carbon Dots in Analytical Chemistry

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Author :
Publisher : Elsevier
ISBN 13 : 0323985734
Total Pages : 366 pages
Book Rating : 4.3/5 (239 download)

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Book Synopsis Carbon Dots in Analytical Chemistry by : Suresh Kumar Kailasa

Download or read book Carbon Dots in Analytical Chemistry written by Suresh Kumar Kailasa and published by Elsevier. This book was released on 2022-08-30 with total page 366 pages. Available in PDF, EPUB and Kindle. Book excerpt: Carbon Dots in Analytical Chemistry: Detection and Imaging explores recent progress in the field of carbon dots synthesis and properties and their integration with various miniaturized analytical devices for the detection of chemical species and imaging of cells. This book is dedicated to exploring the potential applications of carbon dots in analytical chemistry for clinical microbiology, pharmaceutical analysis and environmental analysis. Sections cover synthetic approaches and properties, sample preparation, analytical techniques for the detection of chemical species, imaging of molecules and cells, and analytical tools for biomedical and food analysis. The will be a valuable book for analytical and materials scientists, physical and chemical scientists, and engineers investigating the use of carbon nanomaterials in their analytical procedures. Provides basic knowledge on the preparation and properties of carbon dots and their uses to remove toxic chemical species Integrates knowledge from the fabrication, mechanics, materials science and reliability points-of-view Covers carbon-dot-based optical methods for assaying trace-level target analytes