Journal of Chemistry

Volume 2013 (2013), Article ID 494706, 7 pages

http://dx.doi.org/10.1155/2013/494706

Research Article

Molecular Modeling and Spectroscopic Studies on the Interaction of Transresveratrol with Bovine Serum Albumin

Xiaoli Liu,1,2 Yonghui Shang,³ Xudong Ren,⁴ and Hua Li⁴

¹College of Life Sciences, Northwest University, Xi'an 710069, China

²College of Environmental Science and Engineering, Chang'an University, Xi'an 710054, China

³Department of Chemistry, Xianyang Normal College, Xianyang 712000, China

⁴College of Chemistry and Materials Science, Northwest University, Xi'an 710069, China

Received 7 January 2013; Revised 25 February 2013; Accepted 2 March 2013

Academic Editor: André Silva Pimentel

Copyright © 2013 Xiaoli Liu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The interaction of transresveratrol (TRES) with bovine serum albumin (BSA) has been investigated by ultraviolet-visible, fluorescence, Fourier transform infrared spectroscopic methods and molecular modeling techniques. The fluorescence results show that the intrinsic fluorescence of BSA is quenched by TRES through a static quenching procedure. The binding constants of TRES with BSA at 292, 297 and 302 K are calculated as , , and  L , respectively, and corresponding numbers of binding sites are approximately equal to unity. The thermodynamic parameters ΔH and ΔS are estimated to be −21.82 kJ  and +21.15 J  K⁻¹, which indicates that the interaction of TRES with BSA is driven mainly by hydrophobic forces and there are also hydrogen bonds and electrostatic interactions. The competitive experiments suggest that the binding site of TRES to BSA is probably located on site II. The results of infrared spectra show that the binding of TRES with BSA leads to conformational changes of BSA, and the binding stabilizes the α-helix and β-sheet at the cost of a corresponding loss in the β-turn structure of BSA. The results of molecular modeling calculation clarify the binding mode and the binding sites which are in good accordance with the experiment results.

1. Introduction

Serum albumins, the major soluble protein constituents in the blood stream, bind and transport several exogenous and endogenous molecules like fatty acids, nutrients, steroids, and a large list of drugs. The formed complexes are involved in transport and regulatory processes. Since most of the administered drugs bind extensively and reversibly to serum albumins and drugs are transported mainly as complexes with proteins, the biological activities of the drug such as the overall distribution, metabolism, and efficacy in the body are correlated with their affinities towards serum albumins. Therefore, protein-drug interaction has an enormous biological interest and has been found to play a significant role in pharmacology [1]. Among the serum albumins, bovine serum albumin (BSA) is an appropriate protein model for studying the interaction between serum albumins and drugs because of its medically important, unusual ligand-binding properties, low cost, availability, and structural homology with human serum albumin (HSA) [2, 3].

Transresveratrol (trans-3,5,4′-trihydroxystilbene, TRES) is a polyphenolic natural product existing in a variety of plant species including Polygonum cuspidatum, grapes, peanuts, and various berries. TRES has been shown to prevent or slow the progression of a wide variety of diseases, including cancer, cardiovascular disease, ischemic injuries, and Alzheimer’s disease [4–8]. These properties accompanied with the lack of harmful effects make TRES attractive as a phytoalexin. The molecular structure of TRES is provided in Figure 1. So far, most researches are focusing on its pharmacological activities; only a little has been done on the interaction of TRES with serum albumin. Li et al. [9], Wei et al. [10], and Cao et al. [11] had reported the interaction between resveratrol and BSA, but the binding site of TRES on BSA had not been identified, the changes of secondary structure of BSA had not been quantitatively analyzed, and the binding had not been calculated by molecular modeling techniques. In this paper, the interaction of TRES with BSA is investigated in detail with the purpose to provide basic information for pharmaceutical applications of TRES.

Figure 1: Molecular structure of TRES.

In this work, the interaction of TRES with BSA has been investigated under imitated physiological conditions via spectroscopic methods and molecular modeling techniques. Fluorescence and UV-vis spectroscopy were employed to understand the quenching mechanism of BSA-TRES binding. The binding constants, number of binding sites, and thermodynamic parameters have been calculated, and the binding site of TRES on BSA was identified by fluorescence displacement experiments. Furthermore, Fourier transform infrared (FTIR) spectroscopy was used to demonstrate the conformational changes of BSA, and the changes of secondary structure were quantitatively analyzed by the curve fitting method. In addition, the molecular modeling was used to improve the understanding of the interaction of TRES with BSA.

2. Experimental

2.1. Materials

BSA was purchased from Huamei Bioengineering Company (Shanghai, China). TRES was obtained from Xi’an Sino-Herb Biotechnology Company (Xi’an, China). All other reagents were analytical-reagent grade, and double-distilled water was employed for solutions.

2.2. Fluorescence and UV-Vis Experiments

The fluorescence experiments were performed with an F-4500 fluorescence spectrophotometer (Hitachi). For different samples, the concentrations of BSA were constant at 3 × 10⁻⁷ mol L⁻¹ and the concentrations of TRES were alterable and ranged from 0 to 2.4 × 10⁻⁶ mol L⁻¹. Fluorescence quenching spectra were measured at 292, 297 and 302 K with exciting wavelength of 280 nm. The UV-vis absorption experiments were performed on a UV-2450 spectrophotometer (Shimadzu, Japan).

2.3. Displacement Experiments

The displacement experiments were performed using three different site probes, namely, phenylbutazone, flufenamic acid, and digitoxin, for site I, II, and III, respectively. BSA and the site probe were added to colorimeter tube first, and the concentrations were constant at 3 × 10⁻⁷ mol L⁻¹ and 2 × 10⁻⁷ mol L⁻¹, respectively. Then appropriate amount TRES was added to the BSA-phenylbutazone/flufenamic acid/digitoxin systems.

2.4. FTIR Experiments

FTIR spectra were measured on a Vertex 70 FTIR spectrometer (Bruker Optics, Germany). All FTIR spectra were taken via the attenuated total reflection method. The spectra processing procedure involved collecting spectra of Tris-HCl buffer solution, BSA solution, TRES solution, and BSA-TRES solution under the same conditions. Next, the absorbance of the buffer solution was subtracted from the spectrum of the BSA solution to obtain the spectrum of free BSA, and the absorbance of the TRES solution was subtracted from the spectrum of the BSA-TRES solution to obtain the spectrum of the BSA after interaction. At last, the two difference spectra were compared and analyzed.

2.5. Molecular Modeling

The crystal structure of BSA was obtained from protein databank (PDB) (http://www.rcsb.org/pdb, PDB ID: 3V03), the PDB file was imported into AutoDock Tools, all water molecules were removed, and Kollman charges and solvation parameters were added. The initial 3D structures of TRES were generated by ChemSkcteh software, and the geometries of TRES were subsequently optimized using GAMESS software on DFT/B3LYP/6-31G level. AutoDock4.2 (http://autodock.scripps.edu) program was applied to calculate the interaction modes between TRES and BSA. First the grid box was set as 126 × 100 × 126 points with a grid spacing of 0.560 Å, whole protein was covered, and the initial search was carried out. The region of the most populated of the first five clusters was selected as the probable binding region. Then the accurate search was executed in the probable binding region with a smaller grid map. Lamarckian genetic algorithm was applied in the docking. 100 genetic algorithm (GA) runs were performed with the following parameters: population size of 150, maximum number of energy evaluations, and maximum number of 27,000 generations, and other parameters were default. The resulting conformations were clustered using a root-mean-square deviation (RMSD) of 2.0 Å and the clusters were ranked in order of increasing binding energy of the lowest binding energy conformation in each cluster. Finally the lowest energy conformation in the most populated of the first five clusters was used for docking analysis. The output from AutoDock was rendered with PyMOL.

3. Results and Discussion

3.1. Fluorescence Quenching Mechanism

The fluorescence spectra of BSA in the presence of different concentrations of TRES are shown in Figure 2. It is obvious that BSA has a strong fluorescence emission peak at about 347 nm, and the fluorescence intensity decreases gradually with increasing concentration of TRES, which indicates that TRES can interact with BSA and quench its intrinsic fluorescence. Furthermore, there is a slight red shift of maximum emission wavelength occurring with the addition of TRES, implying that the microenvironment around the chromophore of BSA is changed.

Figure 2: Fluorescence quenching spectra of BSA in presence of different concentrations of TRES. = 3.0 × 10⁻⁷ mol L⁻¹; (×10⁻⁷ mol L⁻¹) (1–6): 0, 3, 6, 12, 18, and 24, respectively; ; .

Fluorescence quenching can occur by different mechanisms, usually classified as dynamic quenching and static quenching. In order to clarify the quenching mechanism of TRES on BSA, the Stern-Volmer equation (1) is used to analyze the fluorescence quenching data [12], where and are the fluorescence intensities in the absence and presence of quencher, is the quenching rate constant of the biomolecule, is the average lifetime of the biomolecule in the absence of quencher which equals  s [13], is the Stern-Volmer quenching constant, and [] is the concentration of quencher. One has

Within certain concentration, the curve of versus [] would be linear if the quenching type is single static or dynamic process. The Stern-Volmer curves of TRES with BSA at three different temperatures exhibit good linear relationship within the investigated concentrations, so the values of and can be determined from the slope of regression curve of versus [], and the results are listed in Table 1. For dynamic quenching, the maximum scatter collision quenching constant of various quenchers with the biopolymers is 2.0 × 10¹⁰ L mol⁻¹ s⁻¹. In addition, dynamic and static quenching can be distinguished by temperature dependence of the quenching, the values of decrease with an increasing temperature for static quenching and the reverse result for dynamic quenching. From Table 1, the results show that the values of and decrease with the increasing of temperature and the values of is much greater than 2.0 × 10¹⁰ L mol⁻¹ s⁻¹, which indicates that the probable quenching mechanism of BSA-TRES interaction is initiated by static quenching rather than by dynamic collision [14, 15]. The results are also confirmed by UV-vis experiments as shown in Figure 3. Figure 3 illustrates that the UV-vis absorption spectrum of BSA and the difference absorption spectrum between BSA-TRES and TRES at the same concentration could not be superposed. After interaction with TRES, the absorbance band intensity of BSA at 280 nm decreases and the peak position shows a slight blue shift, suggesting the formation of BSA-TRES complex.

Table 1: Stern-Volmer quenching constants for the interaction of TRES with BSA at different temperatures.

(L mol⁻¹)
(L mol⁻¹ s⁻¹)
Correlation coefficient

292
7.36 × 10⁴
7.36 × 10¹²
0.9978

297
5.27 × 10⁴
5.27 × 10¹²
0.9921

302
4.64 × 10⁴
4.64 × 10¹²
0.9960

Figure 3: UV-vis absorption spectra of BSA , TRES , and the difference spectrum between TRES-BSA and TRES . =  mol L⁻¹; pH = 7.4.

3.2. The Binding Constant and Number of Binding Sites

When small molecules bind independently to a set of equivalent sites on a macromolecule, the binding constant () and the number of binding sites () can be obtained from fluorescence intensity data by [16]

Based on (2), the values of and can be determined from the slope and intercept of the double logarithm regression curve (] versus ), and the corresponding calculated results are listed in Table 2. It is found that the values of decrease with the increasing of temperature, indicating that the stability of BSA-TRES complex reduces with the temperature rising. The values of approximately equal unity, indicating that there is one independent class of binding sites in BSA for TRES.

Table 2: Binding constants and thermodynamic parameters of BSA-TRES interaction at different temperatures.

(L mol⁻¹)

(kJ mol⁻¹)

(J mol⁻¹ K⁻¹)
(kJ mol⁻¹)

292
10.22 × 10⁴
1.03

−28.00

297
8.71 × 10⁴
1.03
−21.82
21.15
−28.10

302
7.59 × 10⁴
1.04

−28.21

3.3. Thermodynamic Analysis and Binding Mode

Thermodynamic parameters relying on temperatures are analyzed to characterize the acting forces between TRES and BSA. Generally speaking, the binding forces between drugs and biomolecules mainly include electrostatic interaction, hydrogen bond, van der Waals interaction, and hydrophobic interaction [17]. Thermodynamic parameters, free energy change (), enthalpy change (), and entropy change () of interaction, are essential to interpret the binding mode of BSA-drugs complexes. When enthalpy change () does not vary significantly in the temperature range studied, both enthalpy change () and entropy change () can be determined from van’t Hoff equation (3). In (3), corresponds to the binding constant at specific temperature and is the gas constant. and can be calculated from the slope and intercept of the regression curve of ln versus 1/. is consequently obtained according to (4). One has

The Values of , , and for the interaction of TRES with BSA are presented in Table 2. The negative value of indicates the binding process is spontaneous. Positive value of is evidence of hydrophobic interactions [18]. In addition, specific electrostatic interaction between ionic species in aqueous solution is also characterized by a positive and a negative . Generally, mainly comes from the large contribution of with little contribution from for electrostatic interaction [19]. However, in this work, mainly comes from the contribution of . Therefore, we infer that hydrophobic interaction might play a major role in the interaction of TRES with BSA, and electrostatic force may also be involved in the binding process. Meanwhile, hydrogen bond can not be excluded as TRES is a polyphenolic compound.

3.4. Identification of Binding Site

Similar to HSA, the globular protein BSA consists of three distinct drug-binding sites [20]. Sudlow et al. have suggested that site I of serum albumin shows affinity for warfarin, phenylbutazone, and so forth and site II for ibuprofen, flufenamic acid, and so forth [21]. Later studies indicated that digitoxin binding is independent of sites I and II and binds to site III [22]. To identify the binding site of TRES on BSA, competition experiments were carried out with phenylbutazone, flufenamic acid, and digitoxin as site probes for site I, II, and III, respectively [23, 24]. According to (2), the experiment data are analyzed and the binding constants of BSA-TRES system in the presence of different site markers are calculated in Table 3. Obviously, flufenamic acid could significantly influence the binding of TRES with BSA, whereas phenylbutazone or digitoxin has a lesser effect on the binding of TRES to BSA. Hence, it can be concluded that TRES is mainly bound to site II (subdomain IIIA) of BSA.

Table 3: Binding constants of competitive experiments ( K,  nm).

Site marker
(L mol⁻¹)

Blank
7.59 × 10⁴
0.9973
1.03

phenylbutazone
6.17 × 10⁴
0.9860
1.01

flufenamic acid
1.17 × 10⁴
0.9794
0.85

digitoxin
6.11 × 10⁴
0.9899
0.98

3.5. Conformation Investigation

To verify whether the conformation of BSA had changed or not in the absence and presence of TRES, FTIR measurements were performed. FTIR spectra of proteins exhibit a number of amide bands due to different vibrations of the peptide moiety. The amide I peak position occurs in the region 1600–1700 cm⁻¹ (mainly C=O stretch) and amide II band in the region 1500–1600 cm⁻¹ (C–N stretch coupled with N–H bending mode). They both have a relationship with the secondary structure of proteins, and amide I band is more sensitive to the change of proteins secondary structure than amide II [25]. The FTIR difference spectra of free BSA and bonded BSA (after binding with TRES) are shown in Figure 4. It is noticed that the peak position of amide I moves from 1651 to 1655 cm⁻¹, and that of amide II shifts from 1541 to 1545 cm⁻¹ in the FTIR spectrum of BSA after addition of TRES. From the shift in peaks position we can confirm that the conformation of BSA has been affected by the addition of TRES.

Figure 4: FTIR difference spectra of BSA in Tris-HCl buffer solution. free BSA ( = 1.0 × 10⁻⁴ mol L⁻¹); bonded BSA ( = 1.0 × 10⁻⁴ mol L⁻¹, = 2.0 × 10⁻⁴ mol L⁻¹). pH = 7.4.

According to the literature [26, 27], The spectral ranges 1610–1640 cm⁻¹, 1640–1650 cm⁻¹, 1650–1659 cm⁻¹, and 1660–1700 cm⁻¹ in the amide I are assigned generally to β-sheet, random coil, α-helical, and β-turn structure, respectively. To analyze quantitatively the protein secondary structure, the infrared self-deconvolution and second derivative resolution enhancement were applied to estimate the number, position, and width of component bands in the region of 1700–1600 cm; then curve fitting procedures were used to get the best Gaussian-shaped curves that fit the original protein spectrum. The percentage of each secondary structure of BSA can be calculated based on the integrated areas of the component bands in amide I, and the results are shown in Figure 5. The results show that before and after the interaction with TRES, the protein major secondary structures had changed, α-helical structure increased from 53% to 57%, β-sheet increased from 22% to 32%, and β-turn structures decreased from 25% to 11%, respectively.

(a)

(b)

Figure 5: Curve-fitted amide I region for FTIR difference spectra of BSA. (a) Free BSA ( = 1.0 × 10⁻⁴ mol L⁻¹); (b) bonded BSA (= 1.0 × 10⁻⁴ mol L⁻¹, = 2.0 × 10⁻⁴ mol L⁻¹). .

3.6. Molecular Modeling Study

The fluorescence, UV-vis, and FTIR spectroscopic results were complemented with molecular modeling in which TRES was docked to BSA to determine the preferred binding site and the binding mode [28, 29]. In the initial exploration, the results predict that compared with site I and III, the TRES was mostly concentrated in site II with lower binding energy, so site II was selected as the probable binding region. Then the further exploration was carried out with a smaller grid map of points centered at 39.148, 20.061, and 53.329 with a spacing of 0.375 Å at site II. The clustering histogram of further exploration at site II is shown in Figure 6. From Figure 6 we can see that the most populated cluster with 51 conformations has the second lower binding energy, so the lowest binding energy conformation of this cluster is selected and analyzed as the best binding mode. The best energy ranked results of the binding mode between TRES and BAS are shown in Figures 7 and 8. From Figure 7, it can be seen that TRES is located within the binding pocket of subdomain IIIA (site II, the flufenamic acid binding pocket) of the protein and the two rings are not coplanar. In Figure 8, TRES molecule is surrounded by 27 amino acid residues within 6 Å: 14 hydrophobic residues (Leu-387, Leu-407, Leu-453, Leu-430, Leu-457, Ile-388, Phe-403, Phe-488, Gly-431, Gly-434, Val-433, Pro-486, Ala-449, Ala-490), 7 hydrophilic residues (Asn-391, Cys-392, Cys-437, Cys-438, Tyr-411, Ser-435, Ser-489), and 6 ionic residues (Arg-410, Arg-445, Arg-485, Lys-414, Lys-432, Lys-436). It is important to note that the ring of TRES is adjacent to more hydrophobic residues, so hydrophobic forces may play major rule in the binding. Furthermore there are three hydrogen bonds between the hydroxyl groups of TRES and the amino acid residues of BSA; they are 3-OH and Ser-489 with a bond length of 2.0 Å, 5-OH and Arg-410 with a bond length of 2.2 Å, and 4′-OH and Val-433 with a bond length of 2.0 Å. The formation of hydrogen bonds decreases the hydrophilicity and increases the hydrophobicity to stabilize the BSA-TRES system. In addition, electrostatic interactions may play a subordinate role in stabilizing the drug molecule due to the presence of the ionic and polar residues proximity to TRES. Therefore, it can be concluded that the interaction between TRES and BSA is dominated by hydrophobic forces, and there are also hydrogen bonds and electrostatic interactions, which is in good agreement with the results of binding mode study. The calculated binding Gibbs free energy change is −29.95 kJ mol⁻¹ (298 ), which is close to the experimental value (−28.10 kJ mol⁻¹, 297 K) to a certain degree.

Figure 6: The clustering histogram at site II (RMSD: 2.0 Å).

Figure 7: Best conformation for TRES docked to BSA. BSA is represented using cartoon ribbons and TRES is represented using ball.

Figure 8: The amino acid residues around TRES within 6 Å. The residues of BAS are represented using line, TRES structure is represented using stick, and the hydrogen bonds are represented using green dashed line.

4. Conclusions

Interaction mechanism of TRES with BSA has been investigated by fluorescence spectroscopic, UV-vis spectroscopic, FTIR spectroscopic methods and molecular modeling techniques. The results show that TRES interacts with BSA through a combination of static quenching. The interaction is a spontaneous process and is driven by enthalpy and entropy together. The main interaction forces are hydrophobic forces accompanied by hydrogen bonds and electrostatic interactions. The secondary structure of BSA is changed after bonding with TRES. TRES can bind to BSA at site II in subdomain IIIA according to displacement experiments and molecular modeling.

Conflict of Interests

The authors declare that they have no conflict of interests with each other, and they also have no conflict of interests with Huamei Bioengineering Company, Xi’an Sino-Herb Biotechnology Company, ChemSkcteh, or GAMESS software.

Acknowledgments

The authors gratefully acknowledge the financial support of this study by the National Natural Science Foundation of China (Grant no. 20975081) and the special fund for basic scientific research of central colleges, Chang’an University (CHD2012JC093).

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