Tan Anmin, Ziegler André, Steinbauer Bernhard, Seelig Joachim
Department of Biophysical Chemistry, Biozentrum, University of Basel, CH-4056 Basel, Switzerland.
Biophys J. 2002 Sep;83(3):1547-56. doi: 10.1016/S0006-3495(02)73924-6.
The partition equilibria of sodium dodecyl sulfate (SDS) and lithium dodecyl sulfate between water and bilayer membranes were investigated with isothermal titration calorimetry and spectroscopic methods (light scattering, (31)P-nuclear magnetic resonance) in the temperature range of 28 degrees C to 56 degrees C. The partitioning of the dodecyl sulfate anion (DS(-)) into the bilayer membrane is energetically favored by an exothermic partition enthalpy of Delta H(O)(D) = -6.0 kcal/mol at 28 degrees C. This is in contrast to nonionic detergents where Delta H(O)(D) is usually positive. The partition enthalpy decreases linearly with increasing temperature and the molar heat capacity is Delta C(O)(P) = -50 +/- 3 cal mol(-1) K(-1). The partition isotherm is nonlinear if the bound detergent is plotted versus the free detergent concentration in bulk solution. This is caused by the electrostatic repulsion between the DS(-) ions inserted into the membrane and those free in solution near the membrane surface. The surface concentration of DS(-) immediately above the plane of binding was hence calculated with the Gouy-Chapman theory, and a strictly linear relationship was obtained between the surface concentration and the extent of DS(-) partitioning. The surface partition constant K describes the chemical equilibrium in the absence of electrostatic effects. For the SDS-membrane equilibrium K was found to be 1.2 x 10(4) M(-1) to 6 x 10(4) M(-1) for the various systems and conditions investigated, very similar to data available for nonionic detergents of the same chain length. The membrane-micelle phase diagram was also studied. Complete membrane solubilization requires a ratio of 2.2 mol SDS bound per mole of total lipid at 56 degrees C. The corresponding equilibrium concentration of SDS free in solution is C (sat)(D,F) approximately 1.7 mM and is slightly below the critical micelles concentration (CMC) = 2.1 mM (at 56 degrees C and 0.11 M buffer). Membrane saturation occurs at approximately 0.3 mol SDS per mol lipid and the equilibrium SDS concentration is C (sat)(D,F)approximately equal 2.2 mM +/- 0.6 mM. SDS translocation across the bilayer is slow at ambient temperature but increases at high temperatures.
在28℃至56℃的温度范围内,采用等温滴定量热法和光谱方法(光散射、³¹P核磁共振)研究了十二烷基硫酸钠(SDS)和十二烷基硫酸锂在水和双层膜之间的分配平衡。在28℃时,十二烷基硫酸根阴离子(DS⁻)分配到双层膜中在能量上是有利的,其分配焓ΔH₀(D)= -6.0 kcal/mol。这与非离子洗涤剂不同,非离子洗涤剂的ΔH₀(D)通常为正值。分配焓随温度升高呈线性下降,摩尔热容为ΔC₀(P)= -50±3 cal mol⁻¹ K⁻¹。如果将结合的洗涤剂与本体溶液中的游离洗涤剂浓度作图,分配等温线是非线性的。这是由插入膜中的DS⁻离子与膜表面附近溶液中游离的DS⁻离子之间的静电排斥引起的。因此,利用古依-查普曼理论计算了结合平面上方DS⁻的表面浓度,并且在表面浓度与DS⁻分配程度之间获得了严格的线性关系。表面分配常数K描述了不存在静电效应时的化学平衡。对于所研究的各种体系和条件,发现SDS - 膜平衡的K为1.2×10⁴ M⁻¹至6×10⁴ M⁻¹,与相同链长的非离子洗涤剂的可用数据非常相似。还研究了膜 - 胶束相图。在56℃时,完全溶解膜需要每摩尔总脂质结合2.2摩尔SDS的比例。溶液中游离SDS的相应平衡浓度为C(sat)(D,F)≈1.7 mM,略低于临界胶束浓度(CMC)= 2.1 mM(在56℃和0.11 M缓冲液中)。膜饱和发生在每摩尔脂质约0.3摩尔SDS时,平衡SDS浓度为C(sat)(D,F)≈2.2 mM±0.6 mM。在环境温度下,SDS跨双层的转运很慢,但在高温下会增加。