Michels David A, Hu Shen, Schoenherr Regine M, Eggertson Michael J, Dovichi Norman J
Department of Chemistry, University of Washington, Seattle, Washington 98195-1700, USA.
Mol Cell Proteomics. 2002 Jan;1(1):69-74. doi: 10.1074/mcp.t100009-mcp200.
We report a system for automated protein analysis. In the system, proteins are labeled with the fluorogenic reagent 3-(2-furoyl)quinoline-2-carboxaldehyde, which reacts with lysine residues and creates a highly fluorescent product. These labeled proteins are analyzed by submicellar capillary electrophoresis at pH 7.5 to perform a first dimension separation. Once the first components migrate from the capillary, a fraction is transferred to a second dimension capillary, where electrophoresis is performed at pH 11.1 to further separate the proteins. Laser-induced fluorescence is used as an ultrasensitive detector of the separated proteins. Successive fractions are transferred from the first dimension capillary to the second dimension capillary for further separation to generate, in serial fashion, a two-dimensional electropherogram. The transfer of fractions is computer-controlled; there is no operator intervention once the sample has been injected. Zeptomoles of labeled proteins are detected, providing exquisite sensitivity.
我们报道了一种用于蛋白质自动分析的系统。在该系统中,蛋白质用荧光试剂3-(2-呋喃甲酰基)喹啉-2-甲醛进行标记,该试剂与赖氨酸残基反应并生成高荧光产物。这些标记的蛋白质通过在pH 7.5的亚胶束毛细管电泳进行分析,以进行一维分离。一旦第一批组分从毛细管中迁移出来,一部分就会转移到二维毛细管中,在pH 11.1下进行电泳以进一步分离蛋白质。激光诱导荧光用作分离蛋白质的超灵敏检测器。连续的组分从一维毛细管转移到二维毛细管进行进一步分离,以连续方式生成二维电泳图。组分的转移由计算机控制;一旦注入样品,就无需操作员干预。可以检测到zeptomole级别的标记蛋白质,灵敏度极高。