Hu G F, Vallee B L
Center for Biochemical and Biophysical Sciences and Medicine, Harvard Medical School, Boston, Massachusetts 02115.
Anal Biochem. 1994 Apr;218(1):185-91. doi: 10.1006/abio.1994.1158.
A gel retardation method for studying the interaction between proteins and carbohydrates employing fluorophore-assisted carbohydrate electrophoresis (FACE) has been developed. A carbohydrate (or carbohydrate mixture) is labeled fluorescently at its reducing end with 8-aminonaphthalene-1,3,6-trisulfonic acid, incubated with its binding protein(s), separated, visualized, and quantified by the FACE system. Protein-bound carbohydrate remains at the top of the high-percentage polyacrylamide gel, whereas free carbohydrate migrates into the gel and is thereby separated. Employing mixtures of carbohydrates, a side-by-side comparison between protein-present and protein-absent samples easily identifies the carbohydrate ligands of the protein. The method proposed provides a rapid, convenient, and visual alternative for screening and identifying protein-carbohydrate interactions. The feasibilities of the method and of the determination of the apparent association constants of protein-carbohydrate complexes were examined by the use of lectins and their known carbohydrate ligands. The potential of determining association constants for proteins and native carbohydrates through competition experiments with unlabeled carbohydrate is also discussed.
已开发出一种利用荧光团辅助碳水化合物电泳(FACE)研究蛋白质与碳水化合物之间相互作用的凝胶阻滞方法。碳水化合物(或碳水化合物混合物)在其还原端用8-氨基萘-1,3,6-三磺酸进行荧光标记,与它的结合蛋白一起孵育,通过FACE系统进行分离、可视化和定量。与蛋白结合的碳水化合物保留在高百分比聚丙烯酰胺凝胶的顶部,而游离碳水化合物则迁移到凝胶中从而被分离。使用碳水化合物混合物时,在有蛋白和无蛋白样品之间进行并排比较可轻松识别该蛋白的碳水化合物配体。所提出的方法为筛选和鉴定蛋白质-碳水化合物相互作用提供了一种快速、便捷且可视化的替代方法。通过使用凝集素及其已知的碳水化合物配体,检验了该方法的可行性以及测定蛋白质-碳水化合物复合物表观缔合常数的可行性。还讨论了通过与未标记碳水化合物的竞争实验来测定蛋白质与天然碳水化合物缔合常数的潜力。