Ciesiolka T, Gabius H J
Max-Planck-Institut für Experimentelle Medizin, Abteilung Chemie, Göttingen, Federal Republic of Germany.
Anal Biochem. 1988 Feb 1;168(2):280-3. doi: 10.1016/0003-2697(88)90319-3.
We have modified the highly sensitive protein assay of C. M. Stoscheck (1987, Anal. Biochem. 160, 301-305), resulting in a further 8- to 10-fold enhancement of sensitivity. This assay, responding to protein quantities with a detection limit of 1 ng, involves the single step of addition of colloidal gold solution, as now commonly used in histochemistry and protein blotting, to the protein sample, followed by simple measurement of the change in absorbance at 590 nm within minutes. By increasing the concentration of the colloidal gold, by using gold sol that has been stabilized with 0.01% polyethylene glycol and adjusted to pH 3.8, and by adapting the assay to microtiter plates, this type of assay can be applied to reliably determine proteins in the complete nanogram range. This assay therefore compares favorably to other assay procedures in terms of rapidity, sensitivity, expense, and lack of interference by many laboratory reagents, although like the others it suffers from the drawback of differences in response of different proteins, which is inherent in dye-binding assays.
我们对C.M.斯托施克(1987年,《分析生物化学》160卷,301 - 305页)的高灵敏度蛋白质检测方法进行了改进,灵敏度进一步提高了8至10倍。该检测方法对蛋白质含量的检测限为1纳克,只需将胶体金溶液(如今在组织化学和蛋白质印迹中常用)加入蛋白质样品这一步骤,随后在几分钟内简单测量590纳米处吸光度的变化即可。通过提高胶体金的浓度,使用用0.01%聚乙二醇稳定并调至pH 3.8的金溶胶,并使检测方法适用于微量滴定板,这种检测方法可用于可靠地测定纳克范围内的蛋白质。因此,这种检测方法在速度、灵敏度、成本以及不受许多实验室试剂干扰方面优于其他检测方法,不过与其他方法一样,它也存在不同蛋白质响应存在差异的缺点,这是染料结合检测法固有的问题。