Wu C S, Chen G C
Cardiovascular Research Institute, University of California, San Francisco 94143-0524.
Anal Biochem. 1989 Feb 15;177(1):178-82. doi: 10.1016/0003-2697(89)90036-5.
Errors in analyzing CD spectra of proteins arising from adsorption loss onto glass surfaces were examined for six proteins: apolipoproteins A-I and E, fibronectin, bovine serum albumin, insulin, and glucagon. Among these, the glycoproteins, apolipoprotein E and fibronectin, adsorbed most onto glass surfaces. Their CD intensities decreased by about 50% when proteins were diluted serially from 1 to 0.01 mg/ml in regular glass-ware and CD was measured in uncoated cells. The other proteins, except glucagon, also showed a certain degree of adsorption. Thus, adsorption loss of proteins onto glass surfaces is common and may lead to serious errors in experimental results. Adsorption can be minimized by using plastic containers and pipet tips, coating the cell with silicone, and wetting the cell before adding the protein solution.
研究了六种蛋白质(载脂蛋白A-I和E、纤连蛋白、牛血清白蛋白、胰岛素和胰高血糖素)在玻璃表面吸附损失导致的蛋白质圆二色光谱分析误差。其中,糖蛋白载脂蛋白E和纤连蛋白在玻璃表面的吸附最多。当在普通玻璃器皿中将蛋白质从1mg/ml连续稀释至0.01mg/ml并在未涂层的细胞中测量圆二色光谱时,它们的圆二色强度降低了约50%。除胰高血糖素外,其他蛋白质也表现出一定程度的吸附。因此,蛋白质在玻璃表面的吸附损失很常见,可能会导致实验结果出现严重误差。使用塑料容器和移液器吸头、用硅酮包被细胞以及在加入蛋白质溶液之前湿润细胞,可以将吸附降至最低。