Karlin Arthur, Wang Chaojian, Li Jing, Xu Qiang
Center for Molecular Recognition, College of Physicians and Surgeons, Columbia University, 630 West 168th Street, New York, NY 10032, USA.
Biotechniques. 2004 Jun;36(6):1010-6. doi: 10.2144/04366RR02.
Avidin was covalently linked to aldehyde-derivatized polyethersulfone membrane filters. These filters were used in Western blot analysis of proteins reacted with biotinylation reagents and electrophoresed in sodium dodecyl sulfate (SDS) on polyacrylamide gels. Electrophoretic transfer from the gels to these filters was in 0.1% SDS, in which the covalently bound avidin retained its biotin-binding capacity. We compared Western blots on avidin-coated membrane filters of biotinylated and nonbiotinylated forms of mouse immunoglobulin G (IgG), mouse IgG heavy chain, muscle-type acetylcholine receptor alpha subunit, and fused alpha and beta subunits of receptor. Biotinylated proteins were captured with high specificity compared to their nonbiotinylated counterparts and sensitively detected on the avidin-coated membranes.
抗生物素蛋白与醛基衍生化的聚醚砜膜滤器共价连接。这些滤器用于蛋白质的蛋白质印迹分析,该蛋白质与生物素化试剂反应,并在聚丙烯酰胺凝胶上的十二烷基硫酸钠(SDS)中进行电泳。从凝胶到这些滤器的电泳转移是在0.1%的SDS中进行的,其中共价结合的抗生物素蛋白保留了其生物素结合能力。我们比较了生物素化和非生物素化形式的小鼠免疫球蛋白G(IgG)、小鼠IgG重链、肌肉型乙酰胆碱受体α亚基以及受体的融合α和β亚基在抗生物素蛋白包被的膜滤器上的蛋白质印迹。与未生物素化的对应物相比,生物素化的蛋白质以高特异性被捕获,并在抗生物素蛋白包被的膜上被灵敏地检测到。