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1.
The binding of quercetin to lysozyme (LYSO) in aqueous solution was investigated by fluorescence spectroscopy, UV-vis absorption
spectroscopy and molecular simulation at pH 7.4. The fluorescence quenching of LYSO by addition of quercetin is due to static
quenching, the binding constants, K
a
, were 3.63 × 104, 3.31 × 104 and 2.85 × 104 L·mol−1 at 288, 298 and 308 K, respectively. The thermodynamic parameters, enthalpy change, ∆H, and entropy change, ∆S, were noted to be −7.56 kJ·mol−1 and 61.07 J·mol−1·K−1. The results indicated that hydrophobic interaction may play a major role in the binding process. The distance r between the donor (LYSO) and acceptor (quercetin) was determined as 3.34 nm by the fluorescence resonance energy transfer.
The synchronous fluorescence spectroscopy showed the polarity around the tryptophan residues increased and the hydrophobicity
decreased. Furthermore, the study of molecular simulation indicated that quercetin could bind to the active site (a pocket
made up of 24 amino-acid residues) of LYSO mainly via hydrophobic interactions and that there were hydrogen interactions between
the residues (Gln 57, Ile 98) of LYSO and quercetin. The accessible surface area (ASA) calculation verified the important
roles of tryptophan (Trp) residues during the binding process. 相似文献
2.
In pH 1.8 ∼ 2.8 weak acid medium, polyvinylpyrrolidone (PVP) and Eosin Y reacted to form complex that could result in Eosin
Y (EY) fluorescence quenching. The maximum quenching wavelength was at 542 nm. The fluorescence quenching (ΔF) was proportional to the concentration of polyvinylpyrrolidone in a certain range. The linear range, the correlation coefficient
and the detection limit were 0.33 ∼ 2.0 μg•mL−1, 0.9994 and 99.6 ng•mL−1, respectively. The influences of the coexistence substances were tested and the results showed that the method had good selectivity.
Therefore, a new method based on fluorescence quenching of eosin Y by PVP for the determination of trace PVP was developed.
The method was sensitive, simple and rapid, which was applied to the determination of trace PVP in the beer with satisfactory
results. The reaction mechanism was also discussed. 相似文献
3.
The interaction between a classic uncoupler (2,4-dinitrophenol, DNP) and bovine serum albumin (BSA) was investigated by fluorescence
spectroscopy under the physiological conditions. The fluorescence quenching constants were calculated by the Stern-Volmer
equation, and based upon the temperature dependence of quenching constants, it was proved that DNP caused a static quenching
of the intrinsic fluorescence of BSA. Owing to the static quenching mechanism, different associative binding constants at
various temperatures were determined and thus the thermodynamic parameters, namely enthalpy (ΔH = −21.12 kJ mol−1) and entropy changes (ΔS = 23.51 J mol−1 K−1) could be calculated based on the binding constants. Moreover, the enthalpy and entropy changes are consistent with the “Enthalpy-Entropy
Compensation” equation obtained from our previous work. The negative enthalpy and positive entropy indicated that the electrostatic
interactions played a major role in DNP-BSA binding process. Site marker competitive displacement experiments were carried
out by using fluorescence and isothermal titration calorimetry (ITC) methods. These results showed that DNP bound with high
affinity to Sudlow’s site I (subdomain IIA) of BSA. The distance (r = 3.78 nm) between donor (BSA) and acceptor (DNP) was obtained according to the mechanism of fluorescence resonance energy
transfer (FRET). Furthermore, the results of synchronous fluorescence and circular dichroism (CD) spectroscopic studies indicated
that the microenvironment and the secondary conformation of BSA were altered. The above results were supported by theoretical
molecular modeling methods. 相似文献
4.
The interaction of a N-methylated diaminotriphenylmethane dye, malachite green, with lysozyme was investigated by fluorescence spectroscopic techniques
under physiological conditions. The binding parameters have been evaluated by fluorescence quenching methods. The results
revealed that malachite green caused the fluorescence quenching of lysozyme through a static quenching procedure. The thermodynamic
parameters like ΔH and ΔS were calculated to be −15.33 kJ mol−1 and 19.47 J mol−1 K−1 according to van’t Hoff equation, respectively, which proves main interaction between malachite green and lysozyme is hydrophobic
forces and hydrogen bond contact. The distance r between donor (lysozyme) and acceptor (malachite green) was obtained to be 3.82 nm according to Fӧrster’s theory. The results
of synchronous fluorescence, UV/vis and three-dimensional fluorescence spectra showed that binding of malachite green with
lysozyme can induce conformational changes in lysozyme. In addition, the effects of common ions on the constants of lysozyme-malachite
green complex were also discussed. 相似文献
5.
Bruno B. Campos Manuel Algarra Joaquim C. G. Esteves da Silva 《Journal of fluorescence》2010,20(1):143-151
A fluorescent hybrid cadmium sulphide quantum dots (QDs) dendrimer nanocomposite (DAB-CdS) synthesised in water and stable
in aqueous solution is described. The dendrimer, DAB-G5 dendrimer (polypropylenimine tetrahexacontaamine) generation 5, a
diaminobutene core with 64 amine terminal primary groups. The maximum of the excitation and emission spectra, Stokes’ shift
and the emission full width of half maximum of this nanocomposite are, respectively: 351, 535, 204 and 212 nm. The fluorescence
time decay was complex and a four component decay time model originated a good fit (χ = 1.20) with the following lifetimes: τ
1 = 657 ps; τ
2 = 10.0 ns; τ
3 = 59.42 ns; and τ
4 = 265 ns. The fluorescence intensity of the nanocomposite is markedly quenched by the presence of nitromethane with a dynamic
Stern-Volmer constant of 25 M−1. The quenching profiles show that about 81% of the CdS QDs are located in the external layer of the dendrimer accessible
to the quencher. PARAFAC analysis of the excitation emission matrices (EEM) acquired as function of the nitromethane concentration
showed a trilinear data structure with only one linearly independent component describing the quenching which allows robust
estimation of the excitation and emission spectra and of the quenching profiles. This water soluble and fluorescent nanocomposite
shows a set of favourable properties to its use in sensor applications. 相似文献
6.
V. I. Gerasimova A. A. Antoshkov Yu. S. Zavorotny D. A. Lemenovskii 《Journal of Applied Spectroscopy》2012,79(2):203-210
Optical properties (photoluminescence and absorption) of Eu(bta)3(B) n (B = H2O or 1,10-phenanthroline) polycrystalline powders and fluoroacrylate polymers (FAPs) impregnated with these compounds using supercritical CO2 (SC CO2) were investigated. It was established that impregnation of Eu(bta)3phen into the FAPs using an SC CO2 solution was difficult to achieve. The type of B (ancillary ligand) and the polymer matrix were shown to influence the temperature quenching of photoluminescence of Eu3+ ions in the range 25–100°C. A comparative analysis of quantum yields (λex = 300 and 380 nm) and photoluminescence decay times (λex = 337.1 nm) for Eu(bta)3B n and for Eu(bta)3B n -doped FAPs was performed. 相似文献
7.
The spectral dependence of Stern–Volmer constants (KSVlK_{SV}^{\lambda} ) for fluorescence quenching by Cu2+ ions in a standard sample of humic acid (HA) (IHSS) with monochromatic excitation (λex = 337.1 nm) conditions has been studied in the spectral range 400–600 nm. This is interpreted within a concept implying that
HA macromolecules possess the property of polydispersity, which means that fluorophore-containing sites are different in terms
of chemical nature and spatial accessibility. Modeling data show that the minimum number of spectral components required for
the simulated spectral dependence of KSVlK_{SV}^{\lambda} to agree as closely as possible with that observed experimentally is three. 相似文献
8.
The synthesis and functionalization of carbon nanoparticles with PEG200 and mercaptosuccinic acid, rendering fluorescent carbon dots, is described. Fluorescent carbon dots (maximum excitation and
emission at 320 and 430 nm, respectively) with average dimension 267 nm were obtained. The lifetime decay of the functionalized
carbon dots is complex and a three component decay time model originated a good fit with the following lifetimes: τ
1 = 2.71 ns; τ
2 = 7.36 ns; τ
3 = 0.38 ns. The fluorescence intensity of the carbon dots is affected by the solvent, pH (apparent pK
a of 7.4 ± 0.2) and iodide (Stern-Volmer constant of 78 ± 2 M−1). 相似文献
9.
The saccharide binding and conformational characterization of a hemagglutinin, a low molecular weight protein from the seeds
of Moringa oleifera was studied using steady state and time resolved fluorescence. The lectin binds sugars LacNAc (K
a = 1380 M−1) and fructose (K
a = 975 M−1), as determined by the fluorescence spectroscopy. It has a single tryptophan per monomer which is exposed on the surface
and is in a strong electropositive environment as revealed by quenching with iodide. Quenching of the fluorescence by acrylamide
involved both static (K
s = 0.216 M−1) and collisional (K
sv = 8.19 M−1) components. The native protein showed two different lifetimes, τ
1 (1.6 ns) and τ
2 (4.36 ns) which decrease and get converted into a single one, (2.21 ns) after quenching with 0.15 M acrylamide. The bimolecular
quenching constant, k
q
was 7.55 × 1011 M−1 s−1. ANS binding studies showed that the native protein has exposed hydrophobic patches which get further exposed at extreme
acidic or alkaline pH. However, they get buried in the interior of the protein in presence of 1 M GdnHCl or urea. 相似文献
10.
We have studied photoluminescence and thermoluminescence (PL and TL) in CaGa2Se4:Eu crystals in the temperature range 77–400 K. We have established that broadband photoluminescence with maximum at 571 nm
is due to intracenter transitions 4f6 5d–4f7 (8S7/2) of the Eu2+ ions. From the temperature dependence of the intensity (log I–103/T), we determined the activation energy (E
a = 0.04 eV) for thermal quenching of photoluminescence. From the thermoluminescence spectra, we determined the trap depths:
0.31, 0.44, 0.53, 0.59 eV. The lifetime of the excited state 4f6 5d of the Eu2+ ions in the CaGa2Se4 crystal found from the luminescence decay kinetics is 3.8 μsec.
Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 76, No. 1, pp. 112–116, January–February, 2009. 相似文献
11.
A novel ligand with double sulfinyl groups, bis(benzylsulfinyl)methane, was synthesized by a new method and its two lanthanide
(III) complexes were synthesized and characterized by element analysis, molar conductivity, coordination titration analysis,
IR, TG-DSC, 1HNMR and UV spectra. The results indicated that the composition of these complexes was REL2.5(ClO4)3·3H2O (RE = Tb (III), Dy (III), L = C6H5CH2SOCH2SOCH2C6H5). The FT-IR results revealed that the perchlorate group was bonded with the lanthanide ion by the oxygen atoms, and the coordination
was bidentate. The fluorescent spectra illustrated that both the Tb (III) and Dy (III) complexes displayed characteristic
fluorescence in solid state, especially for the Tb (III) complex, the peak of 5D4 → 7 F5 of the Tb (III) ion in 544 nm was stronger than that of others. It indicated that the Tb (III) complex could emit purer green
fluorescence. By analysis fluorescence and phosphorescence spectra, it was found that the ligand had the advantage to absorb
energy and transfer it to the Tb (III) and Dy (III) ions. The phosphorescence spectra and fluorescence lifetimes of the complexes
were also measured. 相似文献
12.
Good-quality hexagonal NbSe2 single crystals were prepared. In 2H-NbSe2, superconducting and charge density wave (CDW) transitions were found at T
s = 7.4 K and T
c = 35 K respectively as reported previously. We have noticed that these two transitions are changed to T
c = 42 K and T
s = 6.5 K, in 4H-NbSe2. Thermopower has shown clear anomaly at CDW transitions. The anisotropic upper critical field was calculated as ~3 and 6.3
for 2H- and 4H-single crystals around t = 0.81, where t = T/T
s, from resistivity and explained in terms of coherence length. From the relation, Hc2 (T)=Hc2 (0)[1-t2]H_{\rm c2} (T)=H_{\rm c2} (0)[1-t^2], Hc2l (0)H_{\rm c2}^l (0) was calculated as ~8.15 T and 16.98 T at t = 0.84 in 2H-NbSe2 and 4H-NbSe2 respectively. However, Hc2t (0) = 2.68H_{\rm c2}^t (0) = 2.68T for both single crystals. 相似文献
13.
Glutathione capped CdTe quantum dots (QD) were synthesised using a simple experimental procedure and two samples were subjected
of study (QD550 and QD600). The maximum of the excitation and emission spectra and the emission full width of half maximum of these two QD were: QD550, 307, 550 and 37 nm; QD600, 307, 600 and 39 nm. The steady state fluorescence properties of the two QD undergo variation when the pH of the aqueous
solution is varied and are characterised by different apparent pKa: QD550, 5.2 ± 0.1; QD600, 6.3 ± 0.3. The fluorescence intensity of the QD550 is markedly quenched by the presence of micromolar quantities of Pb(II) ion (Stern–Volmer constant of about 7 × 105 M−1). PARAFAC analysis of the excitation emission matrices (EEM) of QD550 acquired as function of the Pb(II) ion showed that only one linearly independent component describes the quenching of the
QD550 by the Pb(II) ion allowing robust estimation of the excitation and emission spectra and of the quenching profiles. 相似文献
14.
The interaction between thyroxine hormone and 7 hydroxycoumarin (7HC) was investigated using fluorescence quenching method.
The experimental results showed that thyroxine could quench the fluorescence of 7HC by forming the 7HC–thyroxine complex with
static quenching. The apparent binding constants (K) between 7HC and thyroxine were determined to be 1.51 × 104 (297 K) and 9.06 × 103 (310 K). The binding sites (n) 0.98 ± 0.1. The thermodynamic parameters showed that the interaction between 7HC and thyroxine was driven mainly by hydrogen
bonding interactions and van der Waals force. Calibration for thyroxine, based on quenching titration data, was linear in
the concentration range 2.0 × 10−8 to 3.0 × 10−7 mol/l. The relative standard deviation was 2.58% for 2.0 × 10−7 mol/l thyroxine (n = 4) and the 3σ limit of detection was 3.42 × 10−8 mol/l in cationic surfactant CTAB medium. 相似文献
15.
The interactions between N,N′-di(2-hydroxy-3-methyoxy-phenyl-1-methylene)-o-phenyldiamine-mone Zn(II), Nd(III) nitrate (2LZnNd) and bovine serum albumin (BSA) was investigated by various spectroscopic
techniques under physiological conditions. It was proved that the fluorescence quenching of BSA by 2LZnNb was a result of
the formation of a non-fluorescent complex with the binding constants of 3.15 × 105; 2.72 × 105 and 2.44 × 105 M–1 at 298 K, 304 K and 310 K, respectively. A marked increase in the fluorescence anisotropy in the proteinous environments
indicates that BSA introduces motional restriction on the drug molecule. The corresponding thermodynamics parameters ΔH and ΔS were calculated to be –16.36 kJ mol–1 and 43.48 J mol–1 K–1 via van’t Hoff equation. Moreover, the competitive probes experiment revealed that the binding location of 2LZnNb to BSA
is in the hydrophobic pocket of site II. The effect of 2LZnNb on the conformation of BSA has been analyzed by means of CD
spectrum and three-dimensional fluorescence spectra. The results indicate that the conformation of BSA molecules was changed
in the presence of 2LZnNb Schiff base. 相似文献
16.
Jér?me?Michon Sandrine?Frelon Cédric?Garnier Frédéric?Coppin 《Journal of fluorescence》2010,20(2):581-590
The interactions between uranium and four metalloproteins (Apo-HTf, HSA, MT and Apo-EqSF) were investigated using fluorescence
quenching measurements. The combined use of a microplate spectrofluorometer and logarithmic additions of uranium into protein
solutions allowed us to define the fluorescence quenching over a wide range of [U]/[Pi] ratios (from 0.05 to 1150) at physiologically
relevant conditions of pH. Results showed that fluorescence from the four metalloproteins was quenched by UO22+. Stoichiometry reactions, fluorescence quenching mechanisms and complexing properties of metalloproteins, i.e. binding constants and binding sites densities, were determined using classic fluorescence quenching methods and curve-fitting
software (PROSECE). It was demonstrated that in our test conditions, the metalloprotein complexation by uranium could be simulated
by two specific sites (L1 and L2). Results showed that the U(VI)–Apo-HTf complexation constant values (log K1 = 7.7, log K2 = 4.6) were slightly higher than those observed for U(VI)–HSA complex (log K1 = 6.1, log K2 = 4.8), U(VI)–MT complex (log K1 = 6.5, log K2 = 5.6) and U(VI)–Apo-EqsF complex (log K1 = 5.3, log K2 = 3.9). PROSECE fitting studies also showed that the complexing capacities of each protein were different: 550 moles of U(VI)
are complexed by Apo-EqSF while only 28, 10 and 5 moles of U(VI) are complexed by Apo-HTf, HSA and MT, respectively. 相似文献
17.
Hosseini M Ganjali MR Tavakoli M Norouzi P Faridbod F Goldooz H Badiei A 《Journal of fluorescence》2011,21(4):1509-1513
A novel and simple fluorescence enhancement method for selective pyrophosphate(PPi) sensing was proposed based on a 1:1 metal
complex formation between bis(8-hydroxy quinoline-5-solphonat) chloride aluminum(III) (Al(QS)2Cl), (L) and PPi in aqueous solution. The linear response range covers a concentration range of 1.6 × 10−7 to 1.0 × 10−5 mol/L of PPi and the detection limit of 2.3 × 10−8 mol/L. The association constant of L-PPi complex was calculated 2.6 × 105 L/mol. L was found to show selectively and sensitively fluorescence enhancement toward PPi over than I3-, NO3-, CN−, CO32−, Br−, Cl−, F−, H2PO4− and SO42−, which was attributed to higher stability of inorganic complex between pyrophosphate and L. 相似文献
18.
Ana Paula A. Marques Marcos Takashi S. Tanaka Elson Longo Edson R. Leite Ieda Lucia Viana Rosa 《Journal of fluorescence》2011,21(3):893-899
SrMoO4 doped with rare earth are still scarce nowadays and have attracted great attention due to their applications as scintillating
materials in electro-optical like solid-state lasers and optical fibers, for instance. In this work Sr1−xEuxMoO4 powders, where x = 0.01; 0.03 and 0.05, were synthesized by Complex Polymerization (CP) Method. The structural and optical
properties of the SrMoO4:Eu3+ were analyzed by powder X-ray diffraction patterns, Fourier Transform Infra-Red (FTIR), Raman Spectroscopy, and through Photoluminescent
Measurements (PL). Only a crystalline scheelite-type phase was obtained when the powders were heat-treated at 800 °C for 2 h,
2θ = 27.8° (100% peak). The excitation spectra of the SrMoO4:Eu3+ (λEm. = 614 nm) presented the characteristic band of the Eu3 + 5L6 transition at 394 nm and a broad band at around 288 nm ascribed to the charge-transfer from the O (2p) state to the Mo (4d)
one in the SrMoO4 matrix. The emission spectra of the SrMoO4:Eu3+ powders (λExc. = 394 and 288 nm) show the group of sharp emission bands among 523–554 nm and 578–699 nm, assigned to the 5D1→7F0,1and 2 and 5D0→7F0,1,2,3 and 4, respectively. The band related to the 5D0→7F0 transition indicates the presence of Eu3+ site without inversion center. This hypothesis is strengthened by the fact that the band referent to the 5D0→7F2 transition is the most intense in the emission spectra. 相似文献
19.
Water-soluble Mn2+-doped ZnS quantum dots (QDs) were prepared using mercaptoacetic acid as the stabilizer. The optical properties and structure
features were characterized by X-Ray, absorption spectrum, IR spectrum and fluorescence spectrum. In pH 7.8 Tris-HCl buffer,
the QDs emitted strong fluorescence peaked at 590 nm with excitation wavelength at 300 nm. The presence of sulfide anion resulted
in the quenching of fluorescence and the intensity decrease was proportional to the S2− concentration. The linear range was from 2.5 × 10−6 to 3.8 × 10−5 mol L−1 with detection limit as 1.5 × 10−7 mol L−1. Most anions such as F−, Cl−, Br−, I−, CH3CO2
−, ClO4
−, CO3
2−, NO2
−, NO3
−, S2O3
2−, SO3
2− and SO4
2− did not interfere with the determination. Thus a highly selective assay was proposed and applied to the determination of
S2− in discharged water with the recovery of ca. 103%. 相似文献
20.
Ryosuke Nakahara Satomi Kashitani Kumi Hayakawa Yuuki Kitani Takako Yamaguchi Yoshikazu Fujita 《Journal of fluorescence》2009,19(5):769-775
A fluorophotometric method for the determination of hydrogen peroxide (H2O2) using fluorescin was developed. This method was based on the oxidative reaction of fluorescin, a colorless, non-fluorescent
lactoid fluorescein, by H2O2 to give highly fluorescein fluorescence emission. In the determination of H2O2, the calibration curve exhibited linearity over the H2O2 concentration range of 1.5–310 ng mL−1 at an emission wavelength of 525 nm with an excitation of 500 nm and with relative standard deviations (n = 6) of 2.51%, 2.48%, and 1.31% for 3.1 ng mL−1, 30.8 ng mL−1, and for 308 ng mL−1 of H2O2, respectively. The detection limit for H2O2 was 1.9 ng mL−1 six blank determinations was performed (ρ = 6). This proposed method was applied to detection of other reactive oxygen species and nitrogen species (ROS/RNS) such
as singlet oxygen (1O2), hydroxyl radical (•OH), peroxynitrite (ONOO−) etc., and it was possible to detect them with a high sensitivity. In addition, this proposed method was applied to the recovery
tests of H2O2 in calf serum, human saliva, rain water, and wheat noodles; the results were satisfactory. 相似文献