Rabilloud Thierry
Laboratory of Chemistry and Biology of Metals, CNRS UMR 5249 Grenoble, France.
Laboratory of Chemistry and Biology of Metals, Univ. Grenoble Alpes, Grenoble, France.
Electrophoresis. 2016 Oct;37(20):2595-2601. doi: 10.1002/elps.201600270. Epub 2016 Sep 12.
Determination of protein concentration is often an absolute prerequisite in preparing samples for biochemical and proteomic analyses. However, current protein assay methods are not compatible with both reducers and detergents, which are however present simultaneously in most denaturing extraction buffers used in proteomics and electrophoresis, and in particular in SDS electrophoresis. It was found that inclusion of cyclodextrins in a Coomassie blue-based assay made it compatible with detergents, as cyclodextrins complex detergents in a 1:1 molecular ratio. As this type of assay is intrinsically resistant to reducers, a single-step assay that is both detergent and reducer compatible was developed. Depending on the type and concentration of detergents present in the sample buffer, either beta-cyclodextrin or alpha-cyclodextrin can be used, the former being able to complex a wider range of detergents and the latter being able to complex higher amounts of detergents due to its greater solubility in water. Cyclodextrins are used at final concentrations of 2-10 mg/mL in the assay mix. This typically allows to measure samples containing as little as 0.1 mg/mL protein, in the presence of up to 2% detergent and reducers such as 5% mercaptoethanol or 50 mM DTT in a single step with a simple spectrophotometric assay.
蛋白质浓度的测定通常是为生化和蛋白质组学分析制备样品时的绝对前提条件。然而,目前的蛋白质测定方法与还原剂和去污剂都不兼容,而在蛋白质组学和电泳中使用的大多数变性提取缓冲液中,特别是在SDS电泳中,还原剂和去污剂是同时存在的。研究发现,在基于考马斯亮蓝的测定中加入环糊精可使其与去污剂兼容,因为环糊精以1:1的分子比例与去污剂形成复合物。由于这种类型的测定本质上对还原剂具有抗性,因此开发了一种既与去污剂兼容又与还原剂兼容的单步测定方法。根据样品缓冲液中存在的去污剂的类型和浓度,可以使用β-环糊精或α-环糊精,前者能够与更广泛的去污剂形成复合物,而后者由于其在水中的溶解度更高,能够与更多量的去污剂形成复合物。环糊精在测定混合物中的终浓度为2-10mg/mL。这通常允许在一步简单的分光光度测定中,在存在高达2%的去污剂和还原剂(如5%的巯基乙醇或50mM DTT)的情况下,测量低至0.1mg/mL蛋白质的样品。