Anostario M, Li S H, Huang K S
Department of Inflammation/Autoimmuine Disease, Hoffmann-La Roche, Inc., Nutley, New Jersey 07110.
Anal Biochem. 1994 Sep;221(2):317-22. doi: 10.1006/abio.1994.1419.
We describe here a cell-free ligand binding assay for E-selectin. The assay involves immobilizing soluble E-selection onto microtiter plates and incubating with 125I-labeled carcinoembryonic antigen (CEA) which carries the tetrasaccharide sialyl Lewis x (sLex). The bound CEA is eluted by ethylene glycol bis(beta-aminoethyl ether)-N,N,N',N',-tetraacetic acid and monitored by radioactivity. The binding is abolished by preincubation of either CEA with an anti-sLex antibody or E-selectin with a neutralizing anti-E-selectin antibody, indicating that this is an E-selectin/sLex-specific interaction. The binding is Ca2+ and pH dependent (the optimal pH at 7.0) and also requires sialic acid. Removal of sialic acid from CEA by neuraminidase digestion abrogates the binding. When the protein but not carbohydrate constituent of CEA was denatured by reduction and alkylation, the binding was partially eliminated, indicating that the interaction may also be dependent on either protein conformation or carbohydrate orientation. The assay is simple, sensitive, and comparable to other methods as indicated by an IC50 of 1 mM for sLex. Thus, the assay should be useful for screening antagonists and studying E-selectin structure/function.
我们在此描述一种用于E-选择素的无细胞配体结合测定法。该测定法包括将可溶性E-选择素固定在微量滴定板上,并与携带四糖唾液酸化路易斯x(sLex)的125I标记癌胚抗原(CEA)一起孵育。结合的CEA用乙二醇双(β-氨基乙醚)-N,N,N',N'-四乙酸洗脱,并通过放射性监测。通过将CEA与抗sLex抗体预孵育或E-选择素与中和性抗E-选择素抗体预孵育,结合被消除,表明这是一种E-选择素/sLex特异性相互作用。该结合依赖于Ca2+和pH(最佳pH为7.0),并且还需要唾液酸。通过神经氨酸酶消化从CEA中去除唾液酸可消除结合。当CEA的蛋白质而非碳水化合物成分通过还原和烷基化变性时,结合部分消除,表明该相互作用也可能依赖于蛋白质构象或碳水化合物取向。该测定法简单、灵敏,并且如sLex的IC50为1 mM所示,与其他方法相当。因此,该测定法对于筛选拮抗剂和研究E-选择素的结构/功能应该是有用的。