Tjernberg Agneta, Carnö Sofi, Oliv Frida, Benkestock Kurt, Edlund Per-Olof, Griffiths William J, Hallén Dan
Department of Structural Chemistry, Biovitrum AB, SE-112 76 Stockholm, Sweden.
Anal Chem. 2004 Aug 1;76(15):4325-31. doi: 10.1021/ac0497914.
A fully automated biophysical assay based on electrospray ionization mass spectrometry (ESI-MS) for the determination of the dissociation constants (KD) between soluble proteins and low molecular mass ligands is presented. The method can be applied to systems where the relative MS response of the protein and the protein-ligand complexes do not reflect relative concentrations. Thus, the employed approach enables the use of both electrostatically and nonpolar bound complexes. The dynamic range is wider than for most biological assays, which facilitates the process of establishing a structure-activity relationship. This fully automated ESI-MS assay is now routinely used for ligand screening. The entire procedure is described in detail using hGHbp, a 25-kDa extracellular soluble domain of the human growth hormone receptor, as a model protein.
本文介绍了一种基于电喷雾电离质谱(ESI-MS)的全自动生物物理分析方法,用于测定可溶性蛋白质与低分子量配体之间的解离常数(KD)。该方法可应用于蛋白质和蛋白质-配体复合物的相对质谱响应不能反映相对浓度的系统。因此,所采用的方法能够使用静电结合和非极性结合的复合物。其动态范围比大多数生物分析方法更宽,这有助于建立构效关系。这种全自动ESI-MS分析方法现在已常规用于配体筛选。以人生长激素受体25 kDa的细胞外可溶性结构域hGHbp作为模型蛋白,详细描述了整个过程。