Wind T, Stausbøl-Grøn B, Kjaer S, Kahns L, Jensen K H, Clark B F
Department of Biostructural Chemistry, Institute of Molecular and Structural Biology, Aarhus University, Denmark.
J Immunol Methods. 1997 Nov 10;209(1):75-83. doi: 10.1016/s0022-1759(97)00151-8.
Phage displayed repertoires of antibody fragments, either single chain Fv (scFv) or Fab, have become a real alternative to traditional hybridoma technology in the generation of monoclonal antibodies. The steps usually taken in the selection from such repertoires were analysed and the necessity of chemical elution of bound phage-Abs and precipitation of amplified phage particles questioned. By using a semi-synthetic scFv library as a source, phage antibodies recognising a panel of seven antigens were isolated utilising direct bacterial elution of bound phage. Selections against two antigens were subsequently performed with bacterial or chemical elution in parallel and the resulting pools of phage antibodies compared. It is demonstrated that direct bacterial elution can be used when selecting from phage displayed antibody repertoires but that the enrichment of high affinity binders might be jeopardised. In addition, a simplified and more rapid scheme for amplification and use of phage displayed repertoires is described.
噬菌体展示的抗体片段文库,无论是单链Fv(scFv)还是Fab,在单克隆抗体的产生中已成为传统杂交瘤技术的真正替代方法。分析了从此类文库中进行筛选通常采取的步骤,并对结合的噬菌体抗体进行化学洗脱以及扩增的噬菌体颗粒沉淀的必要性提出了质疑。以一个半合成scFv文库为来源,利用结合噬菌体的直接细菌洗脱法,分离出了识别一组七种抗原的噬菌体抗体。随后,针对两种抗原同时采用细菌洗脱或化学洗脱进行筛选,并对所得的噬菌体抗体库进行比较。结果表明,从噬菌体展示的抗体文库中筛选时可以使用直接细菌洗脱法,但高亲和力结合物的富集可能会受到影响。此外,还描述了一种用于噬菌体展示文库扩增和使用的简化且更快速的方案。