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1.
The interaction between imazethapyr (IMA) and bovine serum albumin (BSA) was investigated by fluorescence spectroscopy. The Stern–Volmer quenching constant (KSV) at three temperatures was evaluated in order to determine the quenching mechanism. The dependence of fluorescence quenching on viscosity was also evaluated for this purpose. The results showed that IMA quenches the fluorescence intensity of BSA through a static quenching process. The values of the binding constant for the formed BSA–IMA complex and the number of binding sites were found to be 1.51×105 M?1 and 0.77, respectively, at room temperature. Based on the calculated thermodynamic parameters, the forces that dominate the binding process are hydrogen bonds and van der Waals forces, and the binding process is spontaneous and exothermic. The quenching of protein fluorescence by iodide ion was used to probe the accessibility of tryptophan residues in BSA and the change in accessibility induced by the presence of IMA. According to the obtained results, the BSA–IMA complex is formed in the site where the Trp-134 is located, causing it to become less exposed to the solvent. 相似文献
2.
The interaction between ZnSe nanoparticles (NPs) and bovine serum albumin (BSA) was studied by UV–vis, fluorescence spectroscopic techniques. The results showed that the fluorescence of BSA was strongly quenched by ZnSe NPs and the quenching mechanism was discussed to be a static quenching procedure, which was proved by quenching constant (Kq). The recorded UV–vis data and the fluorescence data quenching by the ZnSe NPs showed that the interaction between them leads to the formation of ZnSe–BSA complex. Based on the synchronous fluorescence spectra, it was established that the conformational change of BSA was induced by the interaction of ZnSe with the tyrosine micro-region of the BSA molecules. Furthermore, the temperature effects on the structural and spectroscopic properties of individual ZnSe NPs and protein and their bioconjugates (ZnSe–BSA) were also researched. It was found that, compared to the monotonic decrease of the individual ZnSe NPs fluorescence intensity, the temperature dependence of the ZnSe–BSA emission had a much more complex behavior, which was highly sensitive to the conformational changes of the protein. 相似文献
3.
The interaction between silver nanoparticles (SNPs) and Bovine Serum Albumin (BSA) was investigated at physiological pH in
an aqueous solution using fluorescence spectroscopy. The analysis of fluorescence spectrum and fluorescence intensity indicates
that SNPs have a strong ability to quench the intrinsic fluorescence of BSA by both static and dynamic quenching mechanisms.
Resonance light scattering (RLS) spectra indicated the formation of a complex between BSA and SNP. The number of binding sites
‘n’ and binding constants ‘K’ were determined at different temperatures based on fluorescence quenching. The thermodynamic
parameters namely ∆H°, ∆G°, ∆S° were calculated at different temperatures and the results indicate that hydrophobic forces are predominant in the SNP-BSA
complex. Negative ∆G° values imply that the binding process is spontaneous. Synchronous fluorescence spectra showed a blue shift which is indicative
of increasing hydrophobicity. 相似文献
4.
Belal H.M. Hussein 《Journal of luminescence》2011,131(5):900-908
The absorption and fluorescence spectra of 7, 8-dihydroxy-4-methylcoumarin (DHMC) in ethanol-water (1:9 v/v) solution at varying pH values were investigated . The interaction between DHMC and bovine serum albumin (BSA) was investigated by fluorescence, FT-IR, and circular dichroism (CD) spectroscopy. The Stern-Volmer quenching constant (KSV), the quenching rate constant of the bimolecular reaction (Kq), the binding constant, and number of binding sites (n) of DHMC with BSA were evaluated. The results showed that DHMC quenches the fluorescence intensity of BSA through a static quenching process. Positive value of entropy change (ΔS) and negative value of enthalpy change (ΔH) of the BSA-DHMC interaction were obtained according to the van't Hoff equation. The interaction between DHMC and BSA was driven mainly by hydrophobic forces. The binding process was spontaneous and exothermic. The binding distance between the tryptophan residue in BSA and the DHMC was found to be about 2.6 nm based on the Förster theory of non-radiation energy transfer. 相似文献
5.
The interaction between promethazine hydrochloride (PMT) and bovine serum albumin (BSA) in vitro was investigated by means of fluorescence spectroscopy and absorption spectroscopy. The fluorescence of BSA was quenched remarkably by PMT and the quenching mechanism was considered as static quenching by forming a complex. The association constants Ka and the number of binding sites n were calculated at different temperatures. The BSA-PMT binding distance was determined to be less than 8 nm, suggesting that energy transfer from BSA to PMT may occur. The thermodynamic parameters of the interaction between PMT and BSA were measured according to the van’t Hoff equation. The enthalpy change (ΔH) and entropy change (ΔS) were calculated to be −23.62 kJ mol−1 and −0.10 J mol−1 K−1, respectively, which indicated that the interaction of PMT with BSA was driven mainly by van der Waals forces and hydrogen bonds. The binding process was a spontaneous process in which Gibbs free energy change (ΔG) was negative. In addition, the results of synchronous fluorescence spectra and three-dimensional fluorescence spectra showed that binding of PMT with BSA can induce conformational changes in BSA. 相似文献
6.
Kumaran Rajendran 《Journal of luminescence》2010,130(7):1203-3869
Interaction of acridinedione dyes with model transport proteins, bovine serum albumin (BSA) in aqueous solution were investigated by fluorescence spectral studies. A fluorescence enhancement was observed on the addition of BSA to photoinduced electron transfer (PET) based acridinedione dyes, which posses C6H4(p-OCH3) in the 9th position of the basic acridinedione ring. On the contrary, the addition of BSA to non-PET based acridinedione dyes with methyl or phenyl substitution in the 9th position does not result in any fluorescence enhancement. The enhancement in the fluorescence intensity is attributed to the suppression of PET process through space between -OCH3 group and the acridinedione moiety is elucidated by steady state fluorescence measurements. The fluorescence anisotropy value (r) of 0.40 reveals that the motion of the dye molecule is highly constrained and is largely confined to the rigid microenvironment of the protein molecule. The binding constant (K) was found to be in the order of 6.0×103 [M]−1, which implies the existence of hydrophobic interaction between the PET based dye and BSA. Time resolved fluorescence lifetime measurements reveal that the PET based acridinedione dye preferably binds in the hydrophobic interior of BSA. 相似文献
7.
Interaction of the flavonoid hesperidin with bovine serum albumin: A fluorescence quenching study 总被引:1,自引:0,他引:1
The interaction between the flavonoid hesperidin and bovine serum albumin (BSA) was investigated by fluorescence and UV/Vis absorption spectroscopy. The results revealed that hesperidin caused the fluorescence quenching of BSA through a static quenching procedure. The hydrophobic and electrostatic interactions play a major role in stabilizing the complex. The binding site number n, and apparent binding constant KA, corresponding thermodynamic parameters ΔGo, ΔHo, ΔSo at different temperatures were calculated. The distance r between donor (BSA) and acceptor (hesperidin) was obtained according to fluorescence resonance energy transfer. The effect of Cu2+, Zn2+, Ni2+, Co2+, and Mn2+ on the binding constants between hesperidin and BSA were studied. The effect of hesperidin on the conformation of BSA was analyzed using synchronous fluorescence spectroscopy and UV/Vis absorption spectroscopy. 相似文献
8.
Wen Xiu Li 《光谱学快报》2013,46(4):210-216
ABSTRACT The interaction of isoquercitrin and bovine serum albumin (BSA) was investigated by means of fluorescence spectroscopy (FS), resonance light scattering spectroscopy (RLS), and ultraviolet spectroscopy (UV). The apparent binding constants (K a) between isoquercitrin and BSA were 5.37 × 105 L mol?1 (293.15 K) and 2.34 × 105 L mol?1 (303.15 K), and the binding site values (n) were 1.18 ± 0.03. According to the Förster theory of non-radiation energy transfer, the binding distances (r) between isoquercitrin and BSA were 1.94 and 1.95 nm at 293.15 K and 303.15 K, respectively. The experimental results showed that the isoquercitrin could be inserted into the BSA, quenching the inner fluorescence by forming the isoquercitrin–BSA complex. The addition of increasing isoquercitrin to BSA solution leads to the gradual enhancement in RLS intensity, exhibiting the formation of the aggregate in solution. It was found that both static quenching and non-radiation energy transfer were the main reasons for the fluorescence quenching. The entropy change and enthalpy change were negative, which indicated that the interaction of isoquercitrin and BSA was driven mainly by van der Waals interactions and hydrogen bonds. The process of binding was a spontaneous process in which Gibbs free energy change was negative. 相似文献
9.
The three flavonoids including naringenin, hesperetin and apigenin binding to bovine serum albumin (BSA) at pH 7.4 was studied by fluorescence quenching, synchronous fluorescence and UV–vis absorption spectroscopic techniques. The results obtained revealed that naringenin, hesperetin and apigenin strongly quenched the intrinsic fluorescence of BSA. The Stern–Volmer curves suggested that these quenching processes were all static quenching processes. At 291 K, the value and the order of the binding constant were KA (naringenin)=4.08×104<KA (hesperetin)=5.40×104≈KA (apigenin)=5.32×104 L mol?1. The main binding force between the flavonoid and BSA was hydrophobic and electrostatic force. According to the Förster theory of non-radiation energy transfer, the binding distances (r0) were obtained as 3.36, 3.47 and 3.30 nm for naringenin–BSA, hesperetin–BSA and apigenin–BSA, respectively. The effect of some common ions such as Fe3+, Cu2+, Mg2+, Mn2+, Zn2+ and Ca2+ on the binding was also studied in detail. The competition binding was also performed. The apparent binding constant (K′A) obtained suggested that one flavonoid had an obvious effect on the binding of another flavonoid to protein when they coexisted in BSA solution. 相似文献
10.
Neslihan Çelebi 《Journal of luminescence》2007,126(1):103-108
The fluorescence quenching of pyronin B and pyronin Y molecules by molecular oxygen in aqueous solution was studied by using steady-state and time-resolved fluorescence and UV-Vis absorption spectroscopy techniques. In order to understand the quenching mechanism, fluorescence decays, absorption and fluorescence spectra of the probes were recorded as a function of the oxygen concentration and temperature. The quenching was found to be appreciable and shows positive deviation in the Stern-Volmer representation obtained from the fluorescence intensity ratio. Fluorescence quenching constants (kq) were calculated from the τo/τ vs. [Q] plots having linear correlation and compared with calculated diffusion-controlled rate constants (kdiff) values. Experimental results were in good agreement with the simultaneous dynamic and static quenching model. 相似文献
11.
Fei Ding 《Journal of luminescence》2009,129(6):650-655
In this paper, the interaction between barbital and bovine serum albumin (BSA) was investigated by the method of fluorescence spectroscopy under simulative physiological conditions. Fluorescence data revealed that the fluorescence quenching of BSA by barbital was the result of the formation of BSA-barbital complex, and the effective quenching constants (Ka) were 1.468×104, 1.445×104 and 1.403×104 M−1 at 297, 303 and 310 K, respectively. The thermodynamic parameters enthalpy change (ΔH) and entropy change (ΔS) for the reaction were calculated to be −2.679 kJ mol−1 and 70.76 J mol−1 K−1, respectively, according to the van’t Hoff equation. The results indicated that hydrophobic and electrostatic interactions were the dominant intermolecular force in stabilizing the complex. The results of synchronous fluorescence spectra showed that binding of barbital with BSA can induce conformational changes in BSA. In addition, the effects of Cu2+ and Zn2+ on the constants of BSA-barbital complex were also discussed. 相似文献
12.
Baosheng Liu Chao Yang Xiaona Yan Jing Wang Yunkai Lv 《Journal of luminescence》2012,132(5):1133-1138
Colistin sulfate (CS) can quench the fluorescence of bovine serum albumin (BSA) in an aqueous solution at pH 7.40. The static fluorescence-quenching process between BSA and CS was confirmed and the binding constant, the number of binding sites and thermodynamic data for the interaction between BSA and CS were also obtained. Results showed that the order of magnitude of binding constant (Ka) was 104, and the number of binding site (n) in the binary system was approximately equal to 1; electrostatic force played an important role on the conjugation reaction between BSA and CS. On the basis of the Förster theory of the resonance energy transfer, the binding distance (r) between CS and BSA was less than 7 nm. Comparing the quenching of protein fluorescence excited at 280 nm and 295 nm and from the site marker replacement experiments, it was shown that the primary CS binding site was located in the sub-domain IIA (site I) of BSA. Synchronous fluorescence spectra clearly revealed that the binding of CS with BSA can induce conformation changes in BSA. In addition, the effects of common metal ions on the binding constants of CS–BSA complex were also discussed. It was shown that, except Cu2+, the high metal ion concentrations improved the CS efficacy. 相似文献
13.
Mohammad Kamruzzaman Al-Mahmnur Alam Sang Hak Lee Young Ho Kim Gyu-Man Kim Sang Hyub Oh 《Journal of luminescence》2012,132(11):3053-3057
A simple and sensitive spectrofluorimetric method was developed to determine trace amounts of bilirubin (BR) using yttrium (Y3+)–norfloxacin (NFLX) complex as a fluorescence (FL) probe. NFLX can form a stable binary complex with Y3+ and markedly enhances the weak FL signal of the NFLX. The FL intensity of the Y3+–NFLX complex decreased significantly in the presence of BR in a buffer solution at pH=7.2. Under optimal conditions, the FL intensity decreased according to the BR concentration and showed a good linear relationship in the range of 0.03–2.3 μg mL?1 of BR with a correlation coefficient of 0.9988. The limit of detection for the determination of BR was 2.8 ng mL?1 with a relative standard deviation (RSD) of 1.55% for five replicate determination of 0.05 μg mL-1 BR. The presented method offers higher sensitivity with simple instrumentation and was applied successfully in detecting BR at low concentrations. 相似文献
14.
The supramolecular interactions between a homologous series of p-sulfonated calix[n]arenes (SCnA, n = 4, 6, 8) as hosts and lomefloxacin (LFLX) were studied by spectrofluorometry. LFLX was found to react with SCnA to produce stable complexes. The fluorescence intensity of the complexes decreased gradually with increasing SCnA concentration. The formation of complexes was further confirmed by 1H NMR studies and molecular modeling calculations. Data of the stability constants and thermodynamic parameters of the obtained complex showed that the stability of the SC8A-LFLX complex is superior to that of SC6A-LFLX and SC4A-LFLX. A mechanism was proposed to explain the inclusion process. 相似文献
15.
Eosin Y belongs to a xanthene group. It is an anionic fluorescent dye. The absorbance and fluorescence of Eosin Y have been
investigated in a series of alkanols (methanol to propanol). When the solvents are added to the aqueous solution of Eosin
Y (EY) the absorbance and fluorescence intensity are enhanced. The alkanols are found to affect the absorption and fluorescence
spectra of the dye. On the basis of solvent adsorption model the binding constants of the dye with alkanols have been estimated.
The interaction of solvent molecule with dye in aqueous solution is specific in nature. The fluorescence quenching of Eosin
Y by the inorganic ions [Fe(CN)6]−3, [Fe(CN)6]−4 and Cl− was also observed. The ions influenced the quenching process to different extents. The rate constants of quenching were calculated
using the Stern-Volmer equation. The equilibrium constant of dye in presence of inorganic ions are determined by Scott equation. 相似文献
16.
Min Xu Feng-Juan Chen Liang Huang Pin-xian Xi Zheng-zhi Zeng 《Journal of luminescence》2011,131(8):1557-1565
The water-soluble Pr (Ⅲ) and Nd (Ⅲ) complexes with an ofloxacin derivative have been prepared and characterized. The single-crystal X-ray diffraction showed that the Pr (III) and Nd (III) complexes have the similar molecular structure. Under physiological pH condition, the effects of [PrL(NO3)2(CH3OH)](NO3) and [NdL(NO3)2(CH3OH)](NO3) on bovine serum albumin (BSA) were examined using fluorescence spectroscopy in combination with UV-vis absorbance and circular dichroism (CD) spectra. The result reveals that the quenching mechanism of fluorescence of BSA by two complexes is a static quenching process and the number of binding sites is about 1 for both. The thermodynamic parameters (ΔH=−14.52 kJ mol−1, ΔS=56.54 J mol−1 K−1 for [PrL(NO3)2(CH3OH)](NO3) and ΔH=−24.63 kJ mol−1, ΔS=22.07 J mol−1 K−1 for [NdL(NO3)2(CH3OH)](NO3)) indicate that hydrophobic and electrostatic interactions are the main binding force in the complexes-BSA system. The binding average distance between complexes and BSA was obtained on the basis of Förster's theory. In addition, it was proved by the CD spectra that the BSA secondary structure was changed in the presence of complexes in an aqueous solution. 相似文献
17.
The fluorescence spectroscopic technique has been efficiently employed to investigate the interaction between bovine serum albumin (BSA) and cetylpyridinium bromide (CPB) under different pH and temperature conditions. The binding constant, number of binding sites, thermodynamic parameters such as ΔG, ΔH, ΔS, and nature of binding forces between BSA and CPB were obtained by measuring the steady state fluorescence quenching of BSA by CPB. The experimental results showed that the fluorescence quenching of BSA by CPB was a result of the formation of CPB-BSA complex. The static quenching was confirmed from the Stern-Volmer quenching constant at different temperatures. The effect of CPB on the conformation of BSA was analyzed using synchronous and three-dimensional fluorescence spectroscopy. pH dependence complex formation between BSA-CPB is due to the interaction between cationic side chain of CPB and the net charge developed on BSA. The distance ‘r’ between BSA and CPB was obtained according to the fluorescence resonance energy transfer. 相似文献
18.
In this paper, the interaction between p-aminoazobenzene (PAAB) and BSA was investigated mainly by fluorescence quenching spectra, circular dichroism (CD) and three-dimensional fluorescence spectra under simulative physiological conditions. It was proved that the fluorescence quenching of BSA by PAAB was mainly a result of the formation of a PAAB-BSA complex. The modified Stern-Volmer quenching constant K a and the corresponding thermodynamic parameters ΔH, ΔG and ΔS at different temperatures were calculated. The results indicated that van der Waals interactions and hydrogen bonds were the predominant intermolecular forces in stabilizing the complex. The distance r?=?4.33 nm between the donor (BSA) and acceptor (PAAB) was obtained according to Förster’s non-radioactive energy transfer theory. The synchronous fluorescence, CD and three-dimensional fluorescence spectral results showed that the hydrophobicity of amino acid residues increased and the losing of α-helix content (from 63.57 to 51.83%) in the presence of PAAB. These revealed that the microenvironment and conformation of BSA were changed in the binding reaction. 相似文献
19.
Qiaoli Yue Lijun Sun Tongfei Shen Xiaohong Gu Shuqiu Zhang Jifeng Liu 《Journal of fluorescence》2013,23(6):1313-1318
In the present work, gold nanocluster (GNC) induced by bovine serum albumin (BSA) was synthesized as a novel fluorescence probe to detect nitrite (NO2 ?) sensitively and selectively. The fluorescence of GNC was found to be quenched effectively by NO2 ?. Under the optimum conditions, it was found that the change of fluorescence intensity was proportional with the concentration of NO2 ? in the linear range of 0.1–50 μM (R?=?0.9990), with a detection limit (S/N?=?3) of 30 nM. The absorption spectroscopy, circular dichroism (CD), and X-ray photoelectron spectroscopy (XPS) studies were employed to discuss the quenching mechanism. In addition, the present approach was successfully applied in real water samples. 相似文献
20.
The fluorescence and ultraviolet spectroscopies were explored to study the interaction between edaravone (EDA) and bovine serum albumin (BSA) under imitated physiological condition. The experimental results show that the fluorescence quenching mechanism between EDA and BSA is a combined quenching (dynamic and static quenching). The binding constants, binding sites, and the corresponding thermodynamic parameters (ΔG, ΔH, and ΔS) of the interaction system were calculated at different temperatures. According to Förster non-radiation energy transfer theory, the binding distance between EDA and BSA was calculated to be 3.10 nm. The effect of EDA on the conformation of BSA was analyzed using synchronous fluorescence spectroscopy. In addition, the effects of some common metal ions Mg2+, Ca2+, Cu2+, and Ni2+ on the binding constant between EDA and BSA were examined. 相似文献