Jiang W, Hearn M T
Department of Biochemistry and Molecular Biology, Monash University, Victoria, Australia.
Anal Biochem. 1996 Nov 1;242(1):45-54. doi: 10.1006/abio.1996.0426.
An investigation into the adsorption behavior under batch equilibrium binding conditions of hen egg white lysozyme (HEWL) with the immobilized metal ion affinity chromatographic adsorbent, Cu(2+)-IDA Sepharose CL-4B, in the presence of high concentrations of NaCl or KCl has been undertaken. When the concentration of NaCl or KCl in the adsorption buffer was < or = 0.2 M, the adsorption data correlated with predictions based on the Langmuir model. However, when the salt concentration was > or = 0.5 M, the adsorption data appeared to follow the Freundlich-Langmuir model under these higher ionic strength conditions. Under elevated ionic strength conditions, the protein-ligand interactions were shown to involve positive cooperativity by Scatchard plot analysis of the experimental data. The number, n, of interacting protein molecules increased with the salt concentration, while the apparent dissociation constant Kd under these high ionic strength conditions was less dependent on the type of salt present in the adsorption buffer. These studies reveal that the binding of Cu(2+)-IDA Sepharose CL-4B to HEWL acceptor molecules under conditions of high ionic strength is characteristic of general heterogeneous interactions, whereby the immobilized metal ion affinity chromatography (IMAC) ligands bind to a protein acceptor undergoing isodesmic indefinite self-association and multisite attachment. As a consequence, these results on the adsorption behavior of HEWL have important general implications for the preparative use of immobilized metal ion affinity adsorbents in packed and expanded bed systems, particularly with regard to the resolution and productivity of the separation for the target protein. In addition, the results from these studies are relevant to investigations involving analytical affinity chromatographic or biosensor assessment of the interaction of proteins with immobilized IMAC ligands when high ionic strength equilibration feedstocks or conditions are employed.
已对蛋清溶菌酶(HEWL)在高浓度NaCl或KCl存在下与固定化金属离子亲和色谱吸附剂Cu(2+)-IDA Sepharose CL-4B在批量平衡结合条件下的吸附行为进行了研究。当吸附缓冲液中NaCl或KCl的浓度≤0.2 M时,吸附数据与基于朗缪尔模型的预测相关。然而,当盐浓度≥0.5 M时,在这些较高离子强度条件下,吸附数据似乎遵循弗罗因德利希-朗缪尔模型。在升高的离子强度条件下,通过对实验数据进行斯卡查德图分析表明,蛋白质-配体相互作用涉及正协同性。相互作用的蛋白质分子数n随盐浓度增加,而在这些高离子强度条件下的表观解离常数Kd对吸附缓冲液中存在盐的类型依赖性较小。这些研究表明,在高离子强度条件下,Cu(2+)-IDA Sepharose CL-4B与HEWL受体分子的结合具有一般异质相互作用的特征,即固定化金属离子亲和色谱(IMAC)配体与经历等键不定自缔合和多位点附着的蛋白质受体结合。因此,这些关于HEWL吸附行为的结果对于固定化金属离子亲和吸附剂在填充床和膨胀床系统中的制备应用具有重要的普遍意义,特别是对于目标蛋白质分离的分辨率和生产率而言。此外,这些研究结果与在采用高离子强度平衡原料或条件时涉及蛋白质与固定化IMAC配体相互作用的分析亲和色谱或生物传感器评估的研究相关。