Quill T A, Hedrick J L
Section of Molecular and Cellular Biology, University of California, Davis 95616, USA.
Arch Biochem Biophys. 1996 Sep 15;333(2):326-32. doi: 10.1006/abbi.1996.0398.
The fertilization layer of Xenopus laevis eggs is formed by the cortical granule lectin binding to its ligand. The binding requires Ca2+, is specific for galactose, and functionally establishes a block to polyspermy at fertilization. We have designed a new enzyme-linked lectin assay for the cortical granule lectin (CGL) ligand which can detect the presence of the CGL ligand at a sensitivity of 1-2 ng/ml. This assay is specifically inhibited with galactose, 50% inhibition at 9.9 mM, and produces a linear response between 2 and 20 ng of jelly adsorbed to the microtiter plate. Using this assay, the CGL ligand was purified through gel filtration, anion-exchange, and CGL affinity chromatography. Hydrolysis of the purified CGL ligand with a series of exoglycosidases showed that a terminal alpha-galactose is the ligand structure required for recognition by CGL.
非洲爪蟾卵的受精层是由皮质颗粒凝集素与其配体结合形成的。这种结合需要Ca2+,对半乳糖具有特异性,并且在功能上建立了受精时对多精入卵的阻断。我们设计了一种针对皮质颗粒凝集素(CGL)配体的新型酶联凝集素测定法,该方法能够以1-2 ng/ml的灵敏度检测CGL配体的存在。该测定法被半乳糖特异性抑制,在9.9 mM时50%被抑制,并且在吸附到微量滴定板上的2至20 ng卵胶之间产生线性响应。使用该测定法,通过凝胶过滤、阴离子交换和CGL亲和色谱法纯化了CGL配体。用一系列外切糖苷酶对纯化的CGL配体进行水解表明,末端α-半乳糖是CGL识别所需的配体结构。