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在空气-水界面具有可调分子间相互作用的β-乳球蛋白和十二烷基硫酸钠混合层。

Mixed layers of β-lactoglobulin and SDS at air-water interfaces with tunable intermolecular interactions.

作者信息

Engelhardt Kathrin, Weichsel Ulrike, Kraft Elena, Segets Doris, Peukert Wolfgang, Braunschweig Björn

机构信息

Institute of Particle Technology (LFG), University of Erlangen-Nuremberg , Cauerstrasse 4, 91058 Erlangen, Germany.

出版信息

J Phys Chem B. 2014 Apr 17;118(15):4098-105. doi: 10.1021/jp501541q. Epub 2014 Apr 8.

Abstract

Mixtures of β-lactoglobulin (BLG) and sodium dodecyl sulfate (SDS) were studied at pH 3.8 and 6.7 under equilibrium conditions. At these pH conditions, BLG carries either a positive or a negative net charge, respectively, which enables tunable electrostatic interactions between anionic SDS surfactants and BLG proteins. For pH 3.8, vibrational sum-frequency generation (SFG) and ellipsometry indicate strong BLG-SDS complex formation at air-water interfaces that is caused by attractive electrostatic interactions. The latter complexes are already formed in the bulk solution which was confirmed by a thermodynamic study of BLG-SDS mixtures using isothermal titration calorimetry (ITC). For acidic conditions we determine from our ITC data an exothermal binding enthalpy of -40 kJ mol(-1). Increasing SDS/BLG molar ratios above 10 leads to a surface excess of SDS and thus to a charge reversal from a positive net charge with BLG as the dominating surface adsorbed species to a negatively charged layer with SDS as the dominating surface species. The latter is evidenced by a pronounced minimum in SFG intensities that is also accompanied by a phase change of O-H stretching bands due to a reorientation of H2O within the local electric field. This phase change which occurs at SDS/BLG molar ratio between 1 and 10 causes a polarity change in SFG intensities from BLG aromatic C-H stretching vibrations. Conclusions from SFG spectra are corroborated by ellipsometry which shows a dramatic increase in layer thicknesses at molar ratios where a charge reversal occurs. The formation of interfacial multilayers comprising SDS-BLG complexes is, thus, caused by cancellation of electrostatic interactions which leads to agglomeration at the interface. In contrast to pH 3.8, behavior of BLG-SDS mixtures at pH 6.7 is different due to repulsive electrostatic interactions between SDS and BLG which lead to a significantly reduced binding enthalpy of -17 kJ mol(-1). Finally, it has to be mentioned that SFG spectra show a coexistence of BLG and SDS molecules at the interface for BLG-SDS molar ratios > 2.

摘要

在平衡条件下,研究了β-乳球蛋白(BLG)与十二烷基硫酸钠(SDS)在pH 3.8和6.7时的混合物。在这些pH条件下,BLG分别带有正净电荷或负净电荷,这使得阴离子SDS表面活性剂与BLG蛋白质之间能够发生可调谐的静电相互作用。对于pH 3.8,振动和频产生(SFG)和椭偏测量表明,在空气-水界面处形成了强烈的BLG-SDS复合物,这是由有吸引力的静电相互作用引起的。通过使用等温滴定量热法(ITC)对BLG-SDS混合物进行热力学研究证实,后者的复合物已在本体溶液中形成。对于酸性条件,我们从ITC数据中确定放热结合焓为-40 kJ mol⁻¹。将SDS/BLG摩尔比增加到10以上会导致SDS在表面过量,从而导致电荷反转,即从以BLG作为主要表面吸附物种的正净电荷转变为以SDS作为主要表面物种的带负电荷层。后者通过SFG强度的明显最小值得到证明,该最小值还伴随着由于局部电场中H₂O的重新取向而导致的O-H伸缩带的相变。这种在SDS/BLG摩尔比在1到10之间发生的相变导致了SFG强度中BLG芳香族C-H伸缩振动的极性变化。SFG光谱的结论得到椭偏测量的证实,椭偏测量表明在发生电荷反转的摩尔比下,层厚度急剧增加。因此,包含SDS-BLG复合物的界面多层的形成是由静电相互作用的抵消引起的,这导致在界面处发生团聚。与pH 3.8相反,由于SDS和BLG之间的排斥性静电相互作用,BLG-SDS混合物在pH 6.7时的行为不同,这导致结合焓显著降低至-17 kJ mol⁻¹。最后,必须提到的是,对于BLG-SDS摩尔比>2,SFG光谱显示界面处存在BLG和SDS分子共存。

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