Moriyama Yoshiko, Takeda Kunio
Department of Applied Chemistry, Okayama University of Science, 1-1 Ridai-cho, Okayama 700-0005, Japan.
Langmuir. 2005 Jun 7;21(12):5524-8. doi: 10.1021/la050252j.
The protective effect of an anionic double-tailed surfactant, sodium bis(2-ethylhexyl)sulfosuccinate (AOT), on the structures of human serum albumin (HSA) and bovine serum albumin (BSA) in their thermal denaturations was examined by means of circular dichroism measurements. The structural changes of these albumins were reversible in the thermal denaturation below 50 degrees C, but became partially irreversible above this temperature. The effect was observed in the thermal denaturation above 50 degrees C. Although the helicity of HSA decreased from 66% to 44% at 65 degrees C in the absence of the surfactant, the decrement of it was restrained in the coexistence of AOT of extremely low concentrations. When the HSA concentration was 10 muM, the maximal protective effect appeared at 0.15 mM AOT. In the coexistence of the surfactant of this concentration, the helicity was maintained at 58% at 65 degrees C, increasing to the original value upon cooling to 25 degrees C. Beyond 0.15 mM AOT, the helicity sharply decreased until 3 mM AOT. A particular AOT concentration required to induce the maximal protective effect ([AOT]REQ) was examined at different HSA concentrations. [AOT]REQ shifted to higher values with an increase of the protein concentration. From the protein concentration dependences of [AOT]REQ, the maximal protection was estimated to require 8.0 and 5.0 AOT ions per a molecule of HSA and BSA, respectively. The AOT concentration, where the protective effect was observed, was too low to form its micelle-like aggregate. Then the protein structures might be stabilized by a cross-linking of surfactant monomers bound to specific sites. These specific sites might exist between a group of nonpolar residues and a positively charged residue located on several sets of amphiphilic helical rods in the proteins. Such a unique function of the double-tailed ionic surfactant is first presented by its characteristic nature as an amphiphilic material.
通过圆二色性测量研究了阴离子双尾表面活性剂双(2-乙基己基)磺基琥珀酸钠(AOT)对人血清白蛋白(HSA)和牛血清白蛋白(BSA)热变性结构的保护作用。在50℃以下的热变性中,这些白蛋白的结构变化是可逆的,但在该温度以上则部分不可逆。在50℃以上的热变性中观察到了这种效应。在没有表面活性剂的情况下,HSA的螺旋度在65℃时从66%降至44%,但在极低浓度AOT共存时,其下降受到抑制。当HSA浓度为10μM时,最大保护作用出现在0.15mM AOT时。在该浓度的表面活性剂共存下,螺旋度在65℃时保持在58%,冷却至25℃时恢复到原始值。超过0.15mM AOT,螺旋度急剧下降,直到3mM AOT。在不同的HSA浓度下研究了诱导最大保护作用所需的特定AOT浓度([AOT]REQ)。[AOT]REQ随着蛋白质浓度的增加而向更高值移动。根据[AOT]REQ对蛋白质浓度的依赖性,估计每分子HSA和BSA分别需要8.0和5.0个AOT离子才能达到最大保护作用。观察到保护作用的AOT浓度太低,无法形成其胶束状聚集体。那么蛋白质结构可能是通过与特定位点结合的表面活性剂单体的交联而稳定的。这些特定位点可能存在于蛋白质中几组两亲性螺旋杆上的一组非极性残基和一个带正电荷的残基之间。这种双尾离子表面活性剂的独特功能首次通过其作为两亲性材料的特性展现出来。