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作 者:杜珙 薛红[2] 陈保生[2] 吴钢[2] 曾武威[2] 白玲[2] 张文成[2]
机构地区:[1]暨南大学附属第二医院,深圳市人民医院,广东省深圳市518020 [2]中国医学科学院医学分子生物学国家重点实验室,北京市100005
出 处:《中国动脉硬化杂志》2003年第5期470-472,共3页Chinese Journal of Arteriosclerosis
基 金:国家攀登计划项目 (G2 0 0 0 0 0 5 6 5 6 9);国家自然科学基金 (39770 16 8)资助
摘 要:从机采浓缩血小板中 ,应用凝胶柱刀豆素A—琼脂糖、肝素—琼脂糖亲和层析与分子筛层析法 ,分离、纯化并得到血小板膜糖蛋白Ⅱb/Ⅲa受体复合物。血小板膜糖蛋白Ⅱb/Ⅲa受体复合物由α、β两个亚单位组成 ,糖蛋白Ⅱb可还原为糖蛋白Ⅱbα(分子量为 12 5kDa)和糖蛋白Ⅱbβ(分子量为 2 3kDa) ,而糖蛋白Ⅲa为一条多肽链 ,分子量为 95kDa ,还原后为 10 8kDa。经不同凝胶亲和层析、凝胶电泳分析 ,得到血小板膜糖蛋白Ⅱb/Ⅲa受体复合物 ,为进一步筛选单克隆抗体和进行药物研发打下了基础。Aim A method has been developed for the rapid isolation of platelet membrane glycoproteins (GP) Ⅱb and Ⅲa. Methods The GP Ⅱb/Ⅲa complex was purified with concanavalin A-sepharose, heparin-sepharose and sephacryl S-300HR chromatography. Results The GP Ⅱb/Ⅲa complex, GP Ⅱb is composed of two disulfide-linked chains, a heavy chain of 125 kDa, called GPⅡbα, and a light chain of 23 kDa, called GP Ⅱbβ, in reduced conditions. The GP Ⅲa is a single polypeptide of 108 kDa in reduced conditions, or 95 kDa in nonreduced conditions. Conclusions Concanavalin A affinity chromatography was used to purify a platelet glycoprotein fraction. The concanavalin A-retained glycoproteins were eluted and adsorbed with a heparin-sepharose column to remove a major contaminant, thrombospondin. Sephacryl S-300 gel filtration was used as the final purification step to remove most fibrinogen and low-molecular-weight contaminants. The GP Ⅱb/Ⅲa complex can be used for the development of its biological products and further study.
关 键 词:生物化学 血小板膜糖蛋白受体复合物的制备 柱层析法 血小板 糖蛋白Ⅱb/Ⅲa受体复合物 凝胶电泳
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