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1.
Interaction of tetrandrine with human serum albumin: a fluorescence quenching study. 总被引:4,自引:0,他引:4
Chun Wang Qiu-Hua Wu Cai-Rui Li Zhi Wang Jing-Jun Ma Xiao-Huan Zang Na-Xin Qin 《Analytical sciences》2007,23(4):429-433
The interaction of tetrandrine with human serum albumin (HSA) was studied by measuring fluorescence quenching spectra, synchronous fluorescence spectra and ultra-violet spectra. The fluorescence quenching spectra of HSA in the presence of tetrandrine showed that tetrandrine quenched the fluorescence of HSA. The quenching constants of tetrandrine on HSA were determined using the Stern-Volmer equation. Static quenching and non-radiation energy transfer were the two main reasons leading to the fluorescence quenching of HSA by tetrandrine. According to the F?rster theory of non-radiation energy transfer, the binding distances (r) and the binding constants (K(A)) were obtained. The thermodynamic parameters obtained in this study revealed that the interaction between tetrandrine and HSA was mainly driven by a hydrophobic force. The conformational changes of HSA were investigated by synchronous spectrum studies. 相似文献
2.
Chibisov A. K. Alfimov M. V. Zakharova G. V. Avakyan V. G. Fedotova T. V. Gutrov V. N. 《Russian Chemical Bulletin》2022,71(2):199-211
Russian Chemical Bulletin - The review is devoted to the structure and photoprocesses in dimers of polymethine dyes and their complexes as objects of supramolecular photochemistry. The results of... 相似文献
3.
The interaction between BSA and epicatechin was studied using fluorescence quenching titrations combined with trilinear decomposition method and excitation-emission matrix(EEM)fluorescence.The resolved spectra were highly similar with the actual ones which indicated that the resolved results were reliable.The relevant parameters of the binding process were obtained by quantifying each substance in the complicated mixtures in situ.The quenching was static quenching,epicatechin had a weak interaction with BSA and the binding site was one.The total concentration and the free concentration of quenchers had different effect on the system.The results demonstrated that the method exploited in this article is a useful tool to investigate complicated interactions,avoiding complicated pretreatment and simplify experimental procedure. 相似文献
4.
Daphnetin (7,8-dihydroxycoumarin), one of the major bioactive components isolated from Daphne koreane Nakai, has been used in traditional Chinese medicine for the treatment of coagulation disorders. It is also a chelator, an antioxidant and a protein kinase inhibitor. In this paper, a combination of intrinsic fluorescence, Fourier transform infrared (FT-IR) spectroscopy and circular dichroic (CD) spectroscopy has been used to characterize the binding between daphnetin and human serum albumin (HSA) under physiological conditions with drug concentrations of 6.7 x 10(-6) - 2.3 x 10(-5) mol x L(-1), and a HSA concentration of 1.5 x 10(-6) mol x L(-1). Changes in the CD spectra and FT-IR spectra were observed upon ligand binding, and the degree of tryptophan fluorescence quenching did change significantly in the complexes. These data have proved the change in protein secondary structure accompanying ligand binding. The change in tryptophan fluorescence intensity was used to determine the binding constants. The thermodynamic parameters, the enthalpy change (DeltaH) and the entropy change (DeltaS) were calculated to be -12.45 kJ x mol(-1)and 52.48 J x mol(-1) x K(-1) according to the van't Hoff equation, which indicated that hydrophobic and electrostatic interactions played the main role in the binding of daphnetin to HSA, in accordance with the results of calculations performed on a Silicon Graphics Ocatane2 workstation. In addition, the binding distance between daphnetin and HSA was obtained (4.02 nm) based on the Forster energy transfer theory. 相似文献
5.
A study has been made on the energy structures and long-wave electronic transitions for linear trinuclear polymethine dyes by the method of additive generating functions. The necessary and sufficient conditions have been established for the occurrence of local levels related to the central nucleus. It is found that the bisvinylene shift is dependent on the structure of the central nucleus in this class of dyes. The relationship fits the available measurements, and it is predicted that there is a positive bridge effect, namely an increase in the bisvinylene shift in trinuclear dyes by comparison with binuclear ones.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 23, No. 1, pp. 10–21, January–February, 1987. 相似文献
6.
Raising the temperature even in a narrow range causes an appreciable fall in the fluorescence intensity for DODC and HIDC polymethine dyes. Quantum-chemical calculations lead one to interpret the temperature effects as due to an increase in the probabilities of rotation around the bonds in the polymethine chain on account of reduction in their orders on excitation.Organic Chemistry Institute, National Academy of Sciences of the Ukraine, 253094 Kiev, ul. Murmanskaya 5, Ukraine. Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 32, No. 4, pp. 220–223, July–August, 1996. Original article submitted November 30, 1995. 相似文献
7.
A. S. Tatikolov L. A. Shvedova Kh. S. Dzhulibekov Zh. A. Krasnaya A. L. Sigan V. A. Kuz'mina 《Russian Chemical Bulletin》1995,44(5):851-857
Photoinduced electron transfer in ion pairs of cation-anion polymethine dyes was studied by flash photolysis. The formation of radicals, which are the products of photoinduced transfer of an electron from an anion to a cation in the ion pairs, was observed during photoexcitation of a number of cation-anion dyes in nonpolar and some weakly polar solvents (in particular, in toluene and chloroform). Photoinduced electron transfer is also observed during triplet sensitization of ion pairs of the cation-anion dyes. The redox potentials of the cations and anions constituting the dyes were measured; the radical yields were compared with the free energies of photoinduced electron transfer. Photoinduced electron transfer in the systems under study was compared with similar process in cyanineborate ion pairs.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 878–884, May, 1995.The authors thank I. Ya. Levitin for help in measuring redox potentials.This work was financially supported by the Russian Foundation for Basic Research (Project No. 93-03-4217). 相似文献
8.
9.
Yan-Jun Hu Yi Liu Li-Xia Zhang Ru-Ming Zhao Song-Sheng Qu 《Journal of Molecular Structure》2005,750(1-3):174-178
We investigated the interaction between colchicine and bovine serum albumin (BSA) by fluorescence and UV–Vis absorption spectroscopy. In the mechanism discussion, it was proved that the fluorescence quenching of BSA by colchicine is a result of the formation of colchicine–BSA complex; van der Waals interactions and hydrogen bonds play a major role in stabilizing the complex. The modified Stern–Volmer quenching constant Ka and corresponding thermodynamic parameters ΔH, ΔG, ΔS at different temperatures were calculated. The distance r between donor (BSA) and acceptor (colchicine) was obtained according to fluorescence resonance energy transfer (FRET). 相似文献
10.
Modified Stern-Volmer equation is obeyed by bovine serum albumin (BSA)-iodide system showing selective quenching of tryptophanyl
fluorescence of BSA. The fraction of accessible protein fluorescence is 0.56 and the effective Stern-Volmer constant is 290
M-1 at pH 7.4 in 0.005 M phosphate buffer at 25°C. Collisional quenching is operative both in the BSA -I−1 system and the model system, tryptophan-I−1. It is supported by the observed relationship between the ratio of quenching rate constants (k
q
) and diffusion coefficients and alsok
q
with bulk viscosity. 相似文献
11.
12.
Wei Q Wu D Du B Li Y Duan C 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2006,63(3):532-535
In this paper, the binding characteristics of human serum albumin (HSA) and m-nitrophenylfluorone (m-NPF)-molybdenum (Mo(VI)) complex have been studied by fluorophotometry. The binding constants are measured at different temperature. Based on the theory of Forster energy transfer, the binding distance and the energy transfer efficiency between m-nitrophenylfluorone-Mo(VI) complex and protein are obtained. According to the thermodynamic parameters, the main sort of binding force can be judged. The results indicate that HSA and m-NPF-Mo(VI) complex have strong interactions. The mechanism of quenching belongs to static quenching and the main sort of binding force is electrostatic gravitation. 相似文献
13.
Study of the interaction of carbamazepine with bovine serum albumin by fluorescence quenching method. 总被引:1,自引:0,他引:1
The interaction between carbamazepine (CBZ) and bovine serum albumin (BSA) was studied using fluorescence spectroscopy (FS) and ultraviolet spectroscopy (UV). The experimental results showed that the CBZ could insert into the BSA and quench the inner fluorescence of BSA by forming the CBZ-BSA complex. It was found that both static quenching and non-radiation energy transfer were the main reasons leading to the fluorescence quenching. The apparent binding constants (K) between CBZ and BSA were found to be 1.8 x 10(4) (27 degrees C) and 2.8 x 10(4) (37 degrees C) and the binding site values (n) were 0.97 (27 degrees C) and 1.01 (37 degrees C), respectively. According to the Forster theory of non-radiation energy transfer, the binding distances (r) between CBZ and BSA were 3.6 nm and 3.4 nm at 27 degrees C and 37 degrees C, respectively. The process of the binding was a spontaneous molecular interaction in which entropy increased and Gibbs free energy decreased, indicating that the interaction between CBZ and BSA was mainly driven by the hydrophobic force. 相似文献
14.
Andrii V. Kulinich Nadezhda A. Derevyanko Alexander A. Ishchenko Stanislav L. Bondarev Valeri N. Knyukshto 《Journal of photochemistry and photobiology. A, Chemistry》2008,200(2-3):106-113
The fluorescent properties of a series of symmetric cationic cyanine dyes and merocyanines with trimethylene bridge connecting N-atom of the indole residue with α-position of the polymethine chain have been explored in detail. It is shown that the constraining group influences their fluorescent properties both by steric and electronic effects. It revealed an essential decrease of the fluorescence quantum yields of the constrained symmetric cyanine dyes in comparison with those of their analogues without bridge group in their chromophore. This effect diminishes essentially at polymethine chain lengthening. In the case of merocyanines the bridge group can cause a decrease as well a substantial increase of their fluorescence quantum yields depending on their type of solvatochromism and solvent polarity. The conclusions made on the basis of the experimental data are in good agreement with the results of semiempirical quantum-chemical calculations. 相似文献
15.
Interaction of human serum albumin with bendroflumethiazide studied by fluorescence spectroscopy 总被引:5,自引:0,他引:5
Pang YH Yang LL Shuang SM Dong C Thompson M 《Journal of photochemistry and photobiology. B, Biology》2005,80(2):139-144
The interactions between bendroflumethiazide (BFTZ) and human serum albumin (HSA) have been studied by fluorescence spectroscopy. Binding constants for drug attachment to the various binding sites of HSA have been measured at different temperatures in physiological buffer solution. The effect of metal ions on BFTZ interaction with HSA was also investigated. The thermodynamic parameters, DeltaH and DeltaS, have been calculated to be 49.28kJmol(-1)>0, and 258.83Jmol(-1)K(-1)>0, respectively. The distance between HSA and BFTZ, r, was determined to be 1.47nm based on F?rster's non-radiative energy transfer theory. The experimental results reveal that BFTZ has a strong ability to quench the intrinsic fluorescence of HSA through a static quenching mechanism. Furthermore, the binding constants between BFTZ and HSA are remarkably independent of temperature, and decrease in the presence of various ions, usually by about 30-55%. Hydrophobic interaction occurs between BFTZ and the sub-domain II A of HSA. 相似文献
16.
Hou X Tong X Dong W Dong C Shuang S 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2007,66(3):552-556
A new synchronous fluorescence scan analysis was developed for the determination of HSA with high sensitivity with a triphenylmethane acid dye methyl blue as a fluorescence probe. When Deltalambda=140 nm, the synchronous fluorescence peak of methyl blue is located at 323 nm and the synchronous fluorescence intensity of the methyl blue is significantly increased in the presence of trace HSA due to the complex formed between methyl blue and HSA at pH 4.1. Under optimal conditions, the calibration graphs are linear over the range 0.03-266.0 and 266.0-665.0 microg mL(-1) for human serum albumin (HSA). Limit of determination were 0.03 microg mL(-1) for HSA. In the detection of HSA in human serum samples, this method gave values close the clinical data got from hospital. 相似文献
17.
A. K. Chibisov M. V. Alfimov G. V. Zakharova L. S. Atabekyan V. G. Avakyan V. G. Plotnikov 《High Energy Chemistry》2017,51(6):440-448
Thiacarbo- and thiadicarbocyanine indolenine and thiazoline polymethine dyes form host?guest complexes with cucurbit[7,8]urils in water. Cucurbit[7]uril forms preferentially 1: 1 and 1: 2 monomeric complexes and cucurbit[8]uril forms 2: 1 and 2: 2 dimeric complexes. On the basis of quantum-chemical calculations, the structure of monomeric and dimeric complexes has been suggested. The complexation manifested itself in absorption, prompt and thermally activated delayed fluorescence spectra, as well as in the triplet?triplet absorption spectra. Dimeric complexes in the triplet state are involved in one-electron oxidation and participate in triplet?triplet energy transfer. 相似文献
18.
19.
The lifetimes of the blue fluorescence from a higher excited state are directly measured to be 80 ± 30 ps for cryptocyanine and 35 ± 15 ps for DTTC in methanolic solution. The relaxation processes associated with electronic excited states are discussed in the case of DTTC. 相似文献
20.
A. Kathiravan R. Renganathan 《Colloids and surfaces. A, Physicochemical and engineering aspects》2008,324(1-3):176-180
The interaction between colloidal TiO2 and bovine serum albumin (BSA) was studied by using absorption and fluorescence spectroscopic methods. The quenching of the intrinsic protein fluorescence in the presence of different concentrations of colloidal TiO2 was analyzed and number of binding sites (n) and apparent binding constant (K) were measured. The quenching mechanism of albumin by colloidal TiO2 is discussed. The energy transfer efficiency (E) and critical transfer distance (R0) were determined. 相似文献