Maher P, Molday R S
Biochim Biophys Acta. 1981 Oct 2;647(2):259-69. doi: 10.1016/0005-2736(81)90254-6.
The binding sites for the lectins wheat germ agglutinin, Ricinus communis agglutinin and concanavalin A on mouse neuroblastoma cell membranes were identified using SDS-gel electrophoresis in combination with fluorescent lectins. Ricinus communis agglutinin and wheat germ agglutinin were found to bind almost exclusively to a single polypeptide with an apparent molecular weight of 30 000. Concanavalin A labeled over 20 different polypeptides, most with molecular weights greater than 50 000. However, when the neuroblastoma cells were treated with concanavalin A so as to internalize all the concanavalin A binding sites visible at the level of the fluorescent microscope and the purified plasma membranes analyzed for their concanavalin A binding polypeptides, only four of the 20 glycopolypeptides were missing or significantly reduced in amount. Thus, these four high molecular weight concanavalin A-binding polypeptides appear to be the major cell surface receptors for concanavalin A. Binding studies with iodinated concanavalin A indicated that these polypeptides represented the high affinity concanavalin A binding sites (Kd = 2 . 10(-7) M). Low affinity concanavalin A binding sites were present on the cell surface after internalization of high affinity concanavalin A binding sites.
运用十二烷基硫酸钠凝胶电泳结合荧光凝集素的方法,鉴定了小麦胚凝集素、蓖麻凝集素和伴刀豆球蛋白A在小鼠神经母细胞瘤细胞膜上的结合位点。结果发现,蓖麻凝集素和小麦胚凝集素几乎只与一条表观分子量为30000的单一多肽结合。伴刀豆球蛋白A标记了20多种不同的多肽,大多数多肽的分子量大于50000。然而,当用伴刀豆球蛋白A处理神经母细胞瘤细胞,使荧光显微镜下可见的所有伴刀豆球蛋白A结合位点内化,并分析纯化的质膜上的伴刀豆球蛋白A结合多肽时,20种糖多肽中只有4种缺失或含量显著减少。因此,这4种高分子量的伴刀豆球蛋白A结合多肽似乎是伴刀豆球蛋白A的主要细胞表面受体。用碘化伴刀豆球蛋白A进行的结合研究表明,这些多肽代表高亲和力的伴刀豆球蛋白A结合位点(解离常数Kd = 2×10⁻⁷ M)。高亲和力的伴刀豆球蛋白A结合位点内化后,细胞表面仍存在低亲和力的伴刀豆球蛋白A结合位点。