Yarmush M L, Antonsen K P, Sundaram S, Yarmush D M
Department of Chemical and Biochemical Engineering, Rutgers University, Piscataway, New Jersey.
Biotechnol Prog. 1992 May-Jun;8(3):168-78. doi: 10.1021/bp00015a001.
Immunoadsorption is a powerful and generalizable method for protein purification that exploits the fine specificity of antigen-antibody interactions. In spite of its potential utility, the more widespread process scale use of immunoadsorption has been limited by the high cost of the antibody and the lack of gentle elution schemes that completely preserve the activity of both the immunoadsorbent and the eluted product. In this report, we review common chemical elution strategies such as pH, ionic strength, chaotropic salts, denaturants, and organic solvents as well as physical techniques such as pressure, electrokinetics, and temperature. In general, selection of elution strategies has largely been an empirical art, balancing stability of the immunoadsorbent and the eluted product and efficiency. The limitations of the available choices demonstrate that more attention must be placed on the antibody. Techniques which assist in the identification or creation of new antibodies with improved binding properties and resistance to degradation, e.g., screening and/or rational protein engineering, are also discussed.
免疫吸附是一种强大且可推广的蛋白质纯化方法,它利用了抗原 - 抗体相互作用的高特异性。尽管具有潜在的实用性,但免疫吸附在更广泛的工艺规模应用中受到了限制,原因在于抗体成本高昂,且缺乏能完全保留免疫吸附剂和洗脱产物活性的温和洗脱方案。在本报告中,我们综述了常见的化学洗脱策略,如pH值、离子强度、离液盐、变性剂和有机溶剂,以及物理技术,如压力、电动学和温度。一般来说,洗脱策略的选择在很大程度上一直是一门经验性的技艺,需要平衡免疫吸附剂和洗脱产物的稳定性以及效率。现有选择的局限性表明,必须更加关注抗体。还讨论了有助于鉴定或创建具有改善结合特性和抗降解能力的新抗体的技术,例如筛选和/或合理的蛋白质工程。