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作 者:谭成[1] 万卫星[1] 张荣军[1] 张莲芬[1] 韩玉珉[2] 金坚[1]
机构地区:[1]江苏省原子医学研究所核医学国家重点实验室,无锡214063 [2]中国科学院生物物理研究所
出 处:《核技术》2000年第5期343-346,共4页Nuclear Techniques
基 金:卫生部科研基金!96-1-344
摘 要:氯胺-T法碘标水蛭素,采用固相饱和法、固相竞争法分析水蛭素与凝血酶-纤维蛋白原复合物的亲和力及定量结合关系,并分析水蛭素-凝血酶-纤维蛋白原复合物形成的时间反应动力学。结果显示,水蛭素可特异地与凝血酶-纤维蛋白原复合物形成三元复合物,它们的分子配比为14∶14∶1(水蛭素:凝血酶:纤维蛋白原)。生理Ca^(2+)浓度是它们的最佳结合环境,水蛭素与凝血酶-纤维蛋白原复合物结合的亲和常数K_a为9.72 ×10~6L/mol;其结合反应可在30-45min达到平衡,提示水蛭素有作为血栓显像配基的可能性。^(125)I-rhirudin was prepared by chloramine-T method. The affinity of rhirudin with thrombin-fibrin complex was analyzed with solid phase saturation method and competitive method. The kinetics of the rhirudin-thromb in-fibrin complex formation was studied too. Results indicated that rhirudin was able to bind with thrombin-fibrin complex as a tenary complex, but not directly with fibrinogen. The molecular binding ratio was 14:14:1 for rhirudin:thrombin:fibrinogen. The affinity constant of rhirudin with thrombin-fibrin complex was 9.72×10~6L/mol, and the physiological Ca^(2+) concentration was their optimal binding environment. The binding reaction of rhirudin with thrombin-fibrin complex could reach the equilibrium in 30 to 45 minutes. All these results indicate that rhirudin is hopefully a new ligand for thrombotic image.
分 类 号:R817.43[医药卫生—影像医学与核医学]
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