Ladam G, Gergely C, Senger B, Decher G, Voegel J C, Schaaf P, Cuisinier F J
Institut Charles Sadron (CNRS-ULP), 6, rue Boussingault, 67083 Strasbourg, France.
Biomacromolecules. 2000 Winter;1(4):674-87. doi: 10.1021/bm005572q.
The interactions between polystyrenesulfonate (PSS)/polyallylamine (PAH) multilayers with human serum albumin (HSA) were investigated by means of scanning angle reflectometry (SAR). We find that albumin adsorbs both on multilayers terminating with PSS (negatively charged) or PAH (positively charged) polyelectrolytes. On films terminating with PSS only, an albumin equivalent monolayer is found whereas when PAH constitutes the outer layer, albumin interacts with the multilayer in such a way as to form a protein film that extends over thicknesses that can be as high as four times the largest dimension of the native albumin molecule. Once the protein film is formed, it is found that when the albumin solution is replaced by a pure buffer solution of same ionic strength as the adsorption solution almost no desorption takes place. On the other hand, when a buffer solution of higher ionic strength is brought in contact with the albumin film, a significant amount of adsorbed proteins is released. One also observes that, for albumin solutions of a given protein concentration, the adsorbed protein amount depends on the ionic strength of the adsorption solution. On surfaces terminating with PAH, the adsorbed protein amount first increases rapidly but passes through a maximum and decreases with the ionic strength. The ionic strength corresponding to the maximum of the adsorbed albumin amount itself depends on the albumin concentration. On the other hand, on films terminating with PSS the adsorbed amount increases with the salt concentration before leveling-off. These results show that the underlying complexity of concentration and pH dependent adsorption/desorption equilibria often simply termed "protein adsorption" is the result of antagonist competing interactions that are mainly of electrostatic origin. We also propose two microscopic models, that are compatible with our experimental observations.
通过扫描角反射法(SAR)研究了聚苯乙烯磺酸盐(PSS)/聚烯丙胺(PAH)多层膜与人血清白蛋白(HSA)之间的相互作用。我们发现白蛋白既吸附在以PSS(带负电荷)或PAH(带正电荷)聚电解质终止的多层膜上。在仅以PSS终止的膜上,发现形成了相当于单层白蛋白的吸附层,而当PAH构成外层时,白蛋白与多层膜相互作用,形成一种蛋白质膜,其延伸厚度可达天然白蛋白分子最大尺寸的四倍之高。一旦形成蛋白质膜,发现当用与吸附溶液离子强度相同的纯缓冲溶液代替白蛋白溶液时,几乎不会发生解吸。另一方面,当将离子强度更高的缓冲溶液与白蛋白膜接触时,会释放出大量吸附的蛋白质。还观察到,对于给定蛋白质浓度的白蛋白溶液,吸附的蛋白质量取决于吸附溶液的离子强度。在以PAH终止的表面上,吸附的蛋白质量首先迅速增加,但经过最大值后随离子强度降低。对应于吸附白蛋白量最大值的离子强度本身取决于白蛋白浓度。另一方面,在以PSS终止的膜上,吸附量在趋于平稳之前随盐浓度增加。这些结果表明,通常简单称为“蛋白质吸附”的浓度和pH依赖性吸附/解吸平衡的潜在复杂性是主要源于静电的拮抗竞争相互作用的结果。我们还提出了两个与我们的实验观察结果相符的微观模型。