Evans D M, Williams K P, Parsons G, Jindal S
PerSeptive Biosystems, Framingham, Massachusetts 01701, USA.
Anal Biochem. 1995 Jul 20;229(1):42-7. doi: 10.1006/abio.1995.1376.
The identification of a lead ligand from a library of compounds for a specific target requires both a selection process and a method to assess relative affinities. Using a tandem-column chromatographic technique, we have developed a novel and rapid method for determination of relative affinities for ligands binding to a specific target molecule. We demonstrate, using known ligands for the lipid A region of lipopolysaccharide, that the relative affinities of these ligands can be determined and may be used to characterize the competitive interaction between ligands for the same target. The method can be adapted toward screening of soluble libraries of peptides and small molecules and those ligands exhibiting a desired affinity can be rapidly selected for further characterization/development.
从化合物库中为特定靶点鉴定先导配体既需要一个筛选过程,也需要一种评估相对亲和力的方法。我们利用串联柱色谱技术开发了一种新颖且快速的方法,用于测定配体与特定靶分子结合的相对亲和力。我们使用脂多糖脂质A区域的已知配体证明,这些配体的相对亲和力可以被测定,并且可用于表征配体之间对同一靶点的竞争性相互作用。该方法可适用于筛选肽和小分子的可溶性文库,并且可以快速选择那些表现出所需亲和力的配体进行进一步表征/开发。