謝湖均 劉程程 孫 強 顧 青 雷群芳 方文軍,*

(1浙江工商大學應(yīng)用化學系，杭州310018；2浙江工商大學食品與生物工程學院，杭州310018；3浙江大學化學系，杭州310028)

季銨鹽型陽離子表面活性劑與牛血清白蛋白的相互作用

謝湖均1,*劉程程1孫 強1顧 青2,*雷群芳3方文軍3,*

(1浙江工商大學應(yīng)用化學系，杭州310018；2浙江工商大學食品與生物工程學院，杭州310018；3浙江大學化學系，杭州310028)

本文合成并表征了三種不同烷基鏈長度的季銨鹽型陽離子表面活性劑：N-十二烷基-N-(2-羥乙基)-N, N-二甲基溴化銨(DHDAB)、N-十四烷基-N-(2-羥乙基)-N,N-二甲基溴化銨(THDAB)、N-十六烷基-N-(2-羥乙基)-N,N-二甲基溴化銨(CHDAB)。采用熒光光譜法、紫外-可見光譜法、動態(tài)光散射法和等溫滴定量熱法對三種表面活性劑與牛血清白蛋白(BSA)的相互作用進行研究。熒光光譜研究表明，三種表面活性劑主要與BSA分子內(nèi)的色氨酸殘基發(fā)生相互作用，導(dǎo)致蛋白質(zhì)的構(gòu)象發(fā)生變化，且表面活性劑烷基鏈越長，與BSA的相互作用就越強。BSA熒光猝滅的主要原因是靜態(tài)猝滅，紫外光譜實驗同樣驗證了靜態(tài)猝滅的存在。等溫滴定量熱法結(jié)果表明低濃度的表面活性劑與BSA主要發(fā)生靜電作用和疏水作用而放熱。動態(tài)光散射結(jié)果表明高濃度的表面活性劑會使BSA結(jié)構(gòu)被破壞。本文揭示了表面活性劑與BSA相互作用的機理，為表面活性劑的廣泛應(yīng)用提供了理論基礎(chǔ)。

表面活性劑；牛血清白蛋白；熒光猝滅；動態(tài)光散射；等溫滴定量熱

1 Introduction

Surfactants and proteins have attracted wide interest in the field of biology,food,medicine and cosmetics1－3.The structure,concentration,solvent,pH,ionic strength and temperature have significant effects on the interactions between surfactants and proteins.The combination of surfactants with proteins often leads to the changes of conformations of proteins and surrounding microenvironment of certain amino acid residues.The main interaction types between ionic surfactants and proteins contain specific binding(electrostatic and hydrophobic interactions)and cooperative binding4－7.The influence of the alkyl chain length and types of surfactants on these interactions have been widely studied8－11.In addition to traditional methods,such as surface tension,conductivity,electrochemical method,viscosity method, etc,some modern techniques containing UV-visible absorption spectroscopy,fluorescence spectroscopy,dynamic light scattering, circular dichroism spectroscopy,small-angle X-ray scattering, electron spin resonance spectroscopy and calorimetry were also employed to get a clear insight into the interactions between surfactants and proteins12－15.

Bovine serum albumin(BSA)is one of the most abundant proteins in mammalian plasma,capable of storing and transporting numerous endogenous and exogenous compounds16.Thus BSA is often employed as a protein model to study the interactions of protein with metal ions,drugs,dyes,surfactants,etc17－20.Study on the interaction mechanisms between proteins and surfactants,as well as the effects of different surfactants on the conformations of proteins,function and aggregation are of great significance for the development of relevant theory and practical applications.

In this manuscript,the interactions between quaternary ammonium surfactants and BSAhave been studied by means of UV-visible(UV-Vis)absorption spectroscopy,fluorescence(FL) spectrometry,dynamic light scattering(DLS)and isothermal titration calorimetry(ITC)methods.The effect of alkyl chain length of surfactants on the interactions have also been discussed and explored.A series of important interaction parameters have been obtained to clarify the interaction mechanisms.

2 Materials and methods

2.1Materials

BSAwas purchased fromAladdin(nitrogen content≥13.5%); trihydroxy aminomethane(Tris)(purity≥99.9%);HCl(concentration 36%－38%);NaCl(purity≥99.5%).Ultra-pure water was used for the preparation of all solutions.Three kinds of quaternary ammonium surfactants:N-dodecyl-N-(2-hydroxyethyl)-N,N-dimethyl ammonium bromide(DHDAB),N-tetradecyl-N-(2-hydroxyethyl)-N,N-dimethyl ammonium bromide(THDAB)and N-cetyl-N-(2-hydroxyethyl)-N,N-dimethyl ammoniu bromide (CHDAB)were synthesized in our laboratory.

The synthesis process is listed below.

Infrared(IR)spectroscopy,1H nuclear magnetic resonance (NMR)analyses and elemental analysis(EA)of the synthesized surfactants were carried out on a NEXES 470 Fourier infrared spectrometer and Bruker Advance 2B 400 MHz NMR spectrometer and Carlabo EA1110 elemental analyzer,respectively. The spectra and EA result are presented in the Supporting Information(Figs.S1－S3,Tables S1－S3,Supporting Information).

IR and NMR spectra of DHDAB are shown in Fig.S1 and EA result of DHDAB is listed in Table S1.The IR characteristic absorption peaks are as follows:3238.3 cm－1(OH),2917.0 cm－1(C―H),1077.0 cm－1(C―N).The information obtained from the NMR spectra is as follows:(CDCl3,400 MHz,289 K)δH,0.85(t,J=6.8 Hz,3H),1.24－1.34(m,18H),1.75(m,2H),3.35(s,6H),3.50(t, J=8.4 Hz,2H),3.76(t,J=4.6 Hz,2H),4.08－4.14(m,2H), 4.30－4.51(m,1H).

IR and NMR spectra of THDAB are shown in Fig.S2 and EA result of THDAB is listed in Table S2.The IR characteristic absorption peaks are as follows:3232.4 cm－1(OH),2914.0 cm－1(C―H),1060.5 cm－1(C―N).The chemical shifts of THDAB are as follows:(CDCl3,400 MHz,289 K)δH,0.86(t,J=6.8 Hz,3H), 1.24－1.33(m,22H),1.73(m,2H),3.34(s,6H),3.51(t,J=8.4 Hz,2H),3.78(t,J=4.6 Hz,2H),4.08－4.12(m,2H),4.62－4.67 (m,1H).

IR and NMR spectra of CHDAB are shown in Fig.S3 and EA result of CHDAB is listed in Table S3.The IR characteristic absorption peaks are as follows:3229.4 cm－1(OH),2914.0 cm－1(C―H),1090.2 cm－1(C―N).The chemical shifts of CHDAB are as follows:(CDCl3,400 MHz,289 K)δH,0.86(t,J=6.6 Hz,3H), 1.21－1.31(m,26H),1.72－1.77(m,2H),3.34(s,6H),3.53(t,J= 8.2 Hz,2H),3.72(t,J=4.6 Hz,2H),4.09－4.13(m,2H),4.31－4.53(m,1H).

The thermogravimetric analysis(TGA)curves are presented in Figs.S4－S6(Supporting Information).TGA results showed that the decomposition temperature is increased with the increase of alkyl chain length of surfactants.

Tris-HCl buffer solution(pH=7.0,containing 0.1 mol·L－1NaCl to maintain ionic strength)was prepared,which was used to prepare 50 μmol·L－1BSA solution and a series of different concentrations of surfactant solutions.

2.2Spectral measurements

The fluorescence spectra were obtained using a RF-5301PC fluorescence spectrophotometer(Shimadzu,Japan)equipped with a 1.0 cm path length quartz cell.The excitation and emission wavelengths of BSA were monitored at 280 and 350 nm,respectively.The excitation and emission slits are 3 nm.Synchronous fluorescence spectra acquired by fixing the difference of excitation and emission wavelength(Δλ)at 15 and 60 nm.All samples were thermostated at 298 K.

The UV-visible absorption spectra were measured on a UV-2450 ultraviolet-visible spectrophotometer(Shimadzu,Japan)at 298 K.The absorption spectra were recorded in the wavelength range from 250 to 350 nm,and a 1.0 cm path length quartz cell was used for the absorbance measurements.

2.3DLS measurements

DLS experiments were performed using a Ζ-sizer nano ZS (Malvern,UK)at 298 K.The concentration of BSA was 5.0 μmol·L－1and all BSA-surfactants mixed solutions went through 0.22 μm micro membrane filter twice.For each concentration of BSA-surfactant mixed solution,particle size was measured three times and the average values are reported.

2.4ITC determination

ITC data were collected on a high precision microcalorimeter VP-ITC(Micro Co.,USA).The enthalpy changes(ΔH)were obtained by injecting surfactant into the 1.4 mL calorimetric cell, in the absence and presence of BSAin Tris-HCl buffer solution at pH=7.0.The experiments were performed by one injection of 10 μL with a 240 s interval between each injection and the temperature was set to 298 K.The surfactant solution in the cell was stirred at 270 r·min－1.

3 Results and discussion

3.1BSA-surfactants interactions by fluorescencespectrometry

Previous studies suggested that the chromophores of BSA including tryptophan(Trp),tyrosine(Tyr)and phenylalanine(Phe) can launch strong intrinsic fluorescence21,22.In present experiments,the excitation and emission wavelengths of BSA were monitored at 280 and 340 nm,respectively(Fig.1).The results showed that three surfactants can lead to the fluorescence quenching,similar to other cationic surfactants23.With the increase of the concentration of surfactant solutions,it showed good fluorescence quenching to BSA,and the blue shift of maximum emission wavelength of BSAwas also observed,which were attributed to the unfold of the BSA structure.Previous researches reported that the interaction information involving the quenching mechanism,binding constant and binding sites between BSA and surfactants can be obtained by analyzing the fluorescence spectra24.On the basis of the fluorescence emission spectra of BSA-surfactants mixed systems,fluorescence intensity ratio(I0/I)can be obtained by the addition of different concentrations of surfactants,where I0and I are the fluorescence intensities of BSAin the absence and presence of quenchers(surfactants),respectively.

Fig.1 Fluorescence emission spectra of BSA(5.0 μmol·L－1)in the surfactants/Tris-HCl buffer systems(T=298 K)

As shown in Fig.2,the fluorescence quenching effect of three surfactants on BSA is related to the alkyl chain length of surfactants,and the surfactants with long alkyl chain length have strong fluorescence quenching effect on BSA.The isoelectric point of BSAwas 4.9,thus the BSAcarries negative charge at the pH value of 7.0.As three kinds of quaternary ammonium surfactants carries positive charge,electrostatic interactions between surfactants and BSA play an important role in the mixed systems25,26.Another important role is the hydrophobic interactions between the hydrophobic carbon chains of the surfactants and the hydrophobic groups of the protein.Three surfactants have same structures of cationic quaternary ammonium moiety and show similar electrostatic interactions with BSA.Thus the main factors affecting the interactions between different surfactants and BSA are hydrophobic interactions.It is interesting to note that a long length of alkyl chain of surfactant can lead to the strong hydrophobic interactions.Therefore,the hydrophobic interaction strength of surfactants follows the order.CHDAB＞THDAB＞DHDAB.The curve of I0/I－surfactant concentration(C)rela-tionship for CHDAB with the longest alkyl chain has an inflection point,after which it changes slowly to the platform;the curve of I0/I－C relationship for THDAB also has a inflection point,and after the inflection point the increase of I0/I tends to be gentle;the curve of I0/I－C surfactant relationship for DHDAB with the shortest alkyl chain does not show a inflection point.The inflexion point,especially with the emergence of the platform,indicates that the combination of surfactants and BSA tends to be complete or the aggregation of surfactants on the surface of BSA gradually tends to be saturated27.

Fig.2 Fluorescence intensity ratio(I0/I)versus concentration of three surfactants(C)

Fluorescence quenching contains static and dynamic quenching28－31,and the static quenching is caused by the formation of a non-fluorescence complex between quencher and fluorophore, while dynamic quenching is caused by collisional encounters between quencher and fluorophore.The fluorescence data were further analyzed via Stern-Volmer equation32,33.

where I0and I are the fluorescence intensity of BSAin the absence and presence of quencher,respectively.Tois the average lifetime of BSA(To=10－8s)34.Kqstands for the quenching rate constant of the biological macromolecule;Ksvis the Stern-Volmer quenching constant.

Fig.3 shows the Stern-Volmer plots of the surfactants interactions with BSAat 289 and 298 K,and the Stern-Volmer quenching constants of three interactions can be found inTable 1.For the lowconcentration linear region of the surfactants,the fluorescence quenching effect of surfactants on the BSAis well accord with the Stern-Volmer equation.In Table 1,Ksvis inversely correlated with temperature and Kqis much greater than the value of the maximum scatter collision quenching constant of 2.0×1010L·mol－1·s－135,36, thus this quenching process is static quenching37.

Fig.3 Stern-Volmer plots of interactions of three surfactants with BSAat 289 and 298 K

The following double-reciprocal formula was used to deal with the experimental data for static quenching interaction38.

where KAis the binding constant between BSAand quencher;n is the number of binding sites.Fig.4 shows the double-reciprocal curve of surfactants interacting with BSA at 289 and 298 K,and the binding constant KAand binding sites n are listed in Table 1.

For different surfactants,both quenching(Ksv)and binding(KA) constants follow the order:CHDAB＞THDAB＞DHDAB.The results indicated that the long alkyl chains of surfactants have the stronger binding interactions with BSA.The numbers of binding sitesofthreesurfactantswithBSAat289and298Karecloseto1.

Synchronous fluorescence spectroscopy can give information about the change of protein microenvironment.A shift of the maximum emission wavelength is involved in the alteration of the polarity in the microenvironment around the chromophore39.Δλ represents the value of the difference between excitation and emission wavelengths.When the values of Δλ are stabilized at 15 and 60 nm,the synchronous fluorescence shows the characteristics of tyrosine and tryptophan residues,respectively40.Since the maximum emission wavelength of residues is related to its environmental polarity,the change of the protein conformation is determined by the analysis of emission wavelength change41. When Δλ was set at 15 nm,the fluorescence intensity decreased obviously with the increase of surfactant concentrations(Figs.5A－7A);when Δλ was set at 60 nm,the fluorescence intensity increased significantly with the increase of surfactants concentrations(Figs.5B to 7B).In addition,the maximum emission wavelength showed a blue shift,which indicated that the microenvironment around Trp residues was disturbed and the hydrophobicity was increased in the presence of surfactants42. The fluorescence intensity of Trp residues was significantly higher than that of Tyr residues,indicating that the main contribution of the intrinsic fluorescence of BSA comes from Trp residues,thus three surfactants mainly interact with Trp residues of BSA.

Table 1 Binding constant(KA),quenching constant(Ksv)and binding sites(n)of surfactants with BSAat 289 and 298 K

Fig.4 Double-reciprocal curve of interactions of three surfactants with BSAat 289 and 298 K

Fig.5 Synchronous fluorescence spectra of BSAin the DHDAB/Tris-HCl buffer system

Fig.6 Synchronous fluorescence spectra of BSAin the THDAB/Tris-HCl buffer system

3.2BSA-surfactants interactions by UV-Vis absorption spectroscopy

Further evidence of static quenching of BSA upon addition of surfactants was provided by UV-visible absorption spectrum data. Collisional encounters between quencher and fluorophore have no effect on the absorption spectra of protein,and they only affect the excited states of the fluorophores.In contrast,the formation of a ground-state complex between quencher and fluorophore can influence on the absorption spectra43,44.Fig.8 shows the UV-visible absorption spectra of BSAin surfactants/Tris-HCl buffer systems. As shown in Fig.8,the intensity of absorption spectra decreases gradually with the increase of surfactant(DHDAB,THDAB and CHDAB)concentrations from 1 to 6,which indicates that surfactants and protein may form complex,and also proves that the fluorescence quenching of BSA is caused by static quenching. While three surfactant solutions without BSA have no absorption peak near 280 nm.

3.3BSA-surfactants interactions by DLS

As shown in Fig.9,the initial particle size of BSA(5.0 μmol·L－1)in the Tris-HCl buffer solution(pH=7.0)at 298 K is about 7.58 nm.The particle size of surfactant-BSAcomplexes gradually grows with the increase of the surfactants concentrations.The particle size of three surfactants-BSA complexes at low concentration(less than 1 mmol·L－1)follows the order:CHDAB＞THDAB＞DHDAB.Moreover,the surfactants with longer alkylchain interact much stronger with BSA.As the concentrations of DHDAB,THDAB and CHDAB reach to 6,2.56 and 1.28 mmol·L－1,it shows the largest particle size of surfactant-BSAcomplexes with the values of 10.76,11.30 and 11.42 nm,respectively.As the surfactant concentrations continue to increase,the particle size of surfactant-BSA complexes began to decline,and finally the particle diameters fall below the initial value,which indicates that the geometry of BSAhas changed.

Fig.7 Synchronous fluorescence spectra of BSAin the CHDAB/Tris-HCl buffer system

3.4BSA-surfactants interactions by ITC

We then determined the CMC values of three surfactants in buffer solution by isothermal titration calorimetry(ITC)45－47.Fig.10 (A,C,E)displays the representative heat flow profiles as a function of time,which is related to 10 μL aliquot injections of three surfactants(80,10 and 1 mmol·L－1)into the cell containing Tris-HCl buffer solution(pH=7.0,T=298 K).The enthalpy changes of surfactants(ΔH)as a function of surfactants concentration are shown in Fig.10(B,D,F).ΔH was calculated by integrating each heat flow peak with time.According to Fig.10(A, C,E),when the first surfactant aliquots are added into the cell, intense endothermic peaks are observed due to the demicellization of surfactants.It is known that the concentrations of three surfactants in the cell at the first injections remain below the CMC. Upon the increase of surfactant concentration in the cell,the intensity of the endothermic peaks decreases drastically owing to the formation of micelles in solution.Further increase of surfactants concentration above the CMC,the intensity of the endothermic peaks keeps constant resulting from the micelle dilution.The CMC values of three surfactants in Tris-HCl buffer solution were determined from the first derivative of the ΔH curve against surfactant concentration.The CMC values of DHDAB,THDAB and CHDAB are around 6.44,0.58 and 0.06 mmol·L－1(Fig.10(B, D,F)),which indicates that the CMC values of surfactants increase with the increase of alkyl chain length of surfactants.

Fig.8 UV-visible spectra of BSA(5.0 μmol·L－1)in surfactants/Tris-HCl buffer systems(T=298 K)

Fig.9 Hydrodynamic diameter(DH)of BSAin surfactants/Tris-HCl buffer systems at 298 K

In the ITC experiments,the blank experiments involving thesurfactants and BSA solutions titration into the buffer solution were separately carried out,which can offset the effects related to the dissociation of surfactant micelles and the dilution of the surfactant micelles.ΔH was then obtained via deducting the dilution effect of surfactants and BSA solution during titration (Fig.11(B,D,F)).The concentrations of surfactants in these ITC experiments are far greater than that of CMC.Several factors may mediate the interaction enthalpy ΔH between surfactants and BSA, including the dissociation of surfactant micelles,the dilution of the surfactant micelles,the interaction between surfactant monomer and BSA,the interaction between micelles and BSA,and the break of the secondary structure of BSA48.

Fig.10 Control experiment showing typical calorimetric titration curves for three surfactants dilution in buffer solution

Heat flow and interaction enthalpy for surfactants solution titration into BSA solution are shown in Fig.11.As shown inFig.11A,the interaction between DHDAB and BSA is an endothermic process in the experimental concentration range.In Fig. 11C,the interaction process between THDAB and BSA was initially exothermic,and then endothermic with the increase of concentration of THDAB.For Fig.11E,the interaction between CHDAB and BSAis an exothermic process.Fig.11(B,D,F)reveal that when the concentrations of three surfactants are less than CMC,the reaction enthalpy between surfactant and BSA is gradually increased with the increase of concentration of three surfactants.In the case of DHDAB,when the concentration of DHDAB goes beyond CMC,the reaction enthalpy decreases until almost zero.In the case of THDAB and CHDAB,when the concentration of surfactant goes beyond CMC,the reaction enthalpy tends to keep constant.

Fig.11 Heat flow and interaction enthalpy for three surfactants solution titration to 5.0 μmol·L－1BSAsolution in pH 7.0 Tris-HCl buffer solution against the concentration of surfactant at 298 K

The BSAcarries negative charge at the pH value of 7.0,thus the electrostatic interaction caused mainly by the polar positive groupsof surfactants and amino acid residues is an exothermic process. While the hydrophobic interaction between the hydrophobic carbon chains of surfactants and the hydrophobic groups of the protein is an exothermic process.The destruction of the hydrated layer structure of polar groups and BSA molecules is an endothermic process49.In addition,the alternation of secondary structure of BSAis an endothermic process50.

The initial titration concentrations of DHDAB,THDAB and CHDAB solution in syringe are 80,10 and 1 mmol·L－1,respectively.In the case of high titration concentration of surfactant (Fig.11A),the exothermic value from the electrostatic attraction and hydrophobic interaction is less than the endothermic value from the destroyed of hydrated layer structure and the change of secondary structure of BSA.When the concentration of surfactant in the cell is higher than CMC,the surfactant micelles is formed, and the electrostatic attraction is weakened.The interaction enthalpy between surfactants and BSA becomes stable at certain concentrations of surfactants.

4 Conclusions

In this manuscript,the interactions between three kinds of quaternary ammonium cationic surfactants with different lengths of alkyl chains(C12,C14and C16)in the Tris-HCl buffer solution (pH=7.0)with BSAhave been investigated by UV-Vis,FL,DLS and ITC.The results showed that the conformation of BSA is changed by the addition of surfactants,and the increase of alkyl chain length of surfactant is beneficial to the binding of BSA. Three quaternary ammonium cationic surfactants have the static quenching effect on the intrinsic fluorescence of BSA and the maximum emission wavelength of BSA occurs blue shift.In the cases of solutions with low surfactant concentrations,the particle size of surfactants-BSA systems is increased with the increase of alkyl chain length of surfactants.While in concentrated surfactant solutions,surfactant is able to destroy the secondary structure of BSA.ITC results indicated that the main force types of interactions between BSAand three surfactants at low concentrations are hydrophobic and electrostatic interactions,and surfactants with long alkyl chain interact with BSA completely at very low concentrations without the break of the secondary structure of BSA.

The results of interaction between BSAand DHDAB,THDAB, CHDAB are similar to the interaction between BSAand traditional quaternary ammonium cationic surfactants:dodecyltrimethylammonium bromide(DTAB),tetradecyltrimethylammonium bromide(TTAB),and cetyltrimethylammonium bromide(CTAB). While,since the existence of―OH group,the electrostatic interaction between DHDAB,THDAB,CHDAB and BSA is stronger than the electrostatic interaction between DTAB,TTAB, CTAB and BSA51.

Supporting Information:The infrared spectra,NMR,EAand TG-DTG curves of DHDAB,THDAB and CHDAB have been included.This information is available free of charge via the internet at http://www.whxb.pku.edu.cn.

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The Interactions between Quaternary Ammonium Cationic Surfactants and Bovine Serum Albumin

XIE Hu-Jun1,*LIU Cheng-Cheng1SUN Qiang1GU Qing2,*LEI Qun-Fang3FANG Wen-Jun3,*
(1Department of Applied Chemistry,Zhejiang Gongshang University,Hangzhou 310018,P.R.China;
2School of Food Science and Biotechnology,Zhejiang Gongshang University,Hangzhou 310018,P.R.China;3Department of Chemistry,Zhejiang University,Hangzhou 310028,P.R.China)

UV-visible(UV-Vis)absorption spectroscopy,fluorescence spectroscopy(FL),dynamic light scattering(DLS)and isothermal titration calorimetry(ITC)were used to study the interactions between bovine serum albumin(BSA)and the three quaternary ammonium surfactants N-dodecyl-N-(2-hydroxyethyl)-N,N-dimethyl ammonium bromide(DHDAB),N-tetradecyl-N-(2-hydroxyethyl)-N,N-dimethyl ammonium bromide (THDAB)and N-cetyl-N-(2-hydroxyethyl)-N,N-dimethyl ammonium bromide(CHDAB).These surfactants quenched the intrinsic fluorescence of BSA,with longer alkyl chains resulting in more significant quenching. This was attributed to static quenching.Further evidence of static quenching was provided by UV-Vis absorption spectroscopy.The particle size of BSA was found to initially increase and then decrease with increasing surfactant concentration.The concentration of surfactant changed the type of interaction mode.This work revealed the mechanism and binding characteristics between surfactants and protein,and provides the basisfor further applications of surfactants.

Surfactants;Bovine serum albumin;Fluorescence quenching;Dynamic light scattering; Isothermal titration calorimetry

O648

10.3866/PKU.WHXB201609231

Received:July 18,2016;Revised:September 22,2016;Published online:September 23,2016.

*Corresponding authors.XIE Hu-Jun,Email:hujunxie@gmail.com;Tel:+86-571-28008974.FANG Wen-Jun,Email:fwjun@zju.edu.cn.

GU Qing,Email:guqing2002@hotamail.com.

The project was supported by the National Natural Science Foundation of China(21203166,21473157),Natural Science Foundation of Zhejiang

Province,China(LY16B030001),and Food Science and Engineering the Most Important Discipline of Zhejiang Province,China(JYTsp2014111).

國家自然科學基金(21203166,21473157),浙江省自然科學基金(LY16B030001)與浙江省重中之重學科食品科學與工程(JYTsp2014111)資助項目