Cong Wei-Tao, Hwang Sun-Young, Jin Li-Tai, Choi Jung-Kap
College of Pharmacy & Research Institute of Drug Development, Chonnam National University, Gwangju, South Korea.
Electrophoresis. 2008 Nov;29(22):4487-94. doi: 10.1002/elps.200800124.
A simple and sensitive fluorescent staining method for the detection of proteins in SDS-PAGE, namely IB (improved 4,4'-dianilino-1,1'-binaphthyl-5,5'-disulfonic acid) stain, is described. Non-covalent hydrophobic probe 4,4'-dianilino-1,1'-binaphthyl-5,5'-disulfonic acid was applied as a fluorescent dye, which can bind to hydrophobic sites in proteins non-specifically. As low as 1 ng of protein band can be detected briefly by 30 min washing followed by 15 min staining without the aiding of stop or destaining step. The sensitivity of the new presented protocol is similar to that of SYPRO Ruby, which has been widely accepted in proteomic research. Comparative analysis of the MS compatibility of IB stain and SYPRO Ruby stain allowed us to address that IB stain is compatible with the downstream of protein identification by PMF.
本文描述了一种用于在SDS-PAGE中检测蛋白质的简单且灵敏的荧光染色方法,即IB(改进的4,4'-二苯胺基-1,1'-联萘-5,5'-二磺酸)染色法。非共价疏水探针4,4'-二苯胺基-1,1'-联萘-5,5'-二磺酸被用作荧光染料,它可以非特异性地结合蛋白质中的疏水位点。只需30分钟洗涤,随后15分钟染色,无需终止或脱色步骤,就能短暂检测到低至1 ng的蛋白条带。新提出的方案的灵敏度与SYPRO Ruby相似,SYPRO Ruby在蛋白质组学研究中已被广泛接受。对IB染色和SYPRO Ruby染色的质谱兼容性进行比较分析,使我们能够确定IB染色与通过PMF进行蛋白质鉴定的下游过程兼容。