Smejkal Gary B, Robinson Myra H, Lazarev Alexander
Proteome Systems, Woburn, MA 01801, USA.
Electrophoresis. 2004 Aug;25(15):2511-9. doi: 10.1002/elps.200406005.
The fluorescence of proteins stained with Deep Purple and SYPRO Ruby was measured over a time course of UV transillumination to determine the relative photostability of each stain. Mean spot fluorescence (n = 200 matched spots) in gels stained with Deep Purple decreased 27% following 2 min of UV transillumination, compared to SYPRO Ruby, which decreased 17%. After 19 min, an 83% decrease in Deep Purple fluorescence was observed, compared to 44% for SYPRO Ruby. By interpolation, the half-life of Deep Purple fluorescence was estimated to be approximately 6 min. The half-life of SYPRO Ruby fluorescence was not reached during the 19 min time course. Further, differential staining of proteins was observed in gels stained with Deep Purple and SYPRO Ruby as compared to colloidal Coomassie Brilliant Blue and silver staining.
在紫外线透射照明的时间进程中测量用深紫和SYPRO Ruby染色的蛋白质的荧光,以确定每种染色剂的相对光稳定性。与SYPRO Ruby相比,用深紫染色的凝胶中的平均斑点荧光(n = 200个匹配斑点)在紫外线透射照明2分钟后下降了27%,而SYPRO Ruby下降了17%。19分钟后,观察到深紫荧光下降了83%,而SYPRO Ruby为44%。通过插值法,深紫荧光的半衰期估计约为6分钟。在19分钟的时间进程中未达到SYPRO Ruby荧光的半衰期。此外,与考马斯亮蓝胶体染色和银染色相比,在用深紫和SYPRO Ruby染色的凝胶中观察到蛋白质的差异染色。