常规的蛋白质碘标方法易引起被标细胞因子的失活,是受体配基竞争结合实验失败的原因之一.试用氯胺-T双相碘标法标记rhG-CSF和rhEPO,并应用受体配基竞争结合分析法测定NFS-60细胞G-CSF受体及BET-2细胞EPO受体的特性.结果显示所获 125I-EPO和 125I-G-CSF放射比活度均较高;发现BET-2细胞有高、低两种亲和力的EPO受体,NFS-60细胞只有一种高亲和力的G-CSF受体,所获结果与文献资料相一致.说明氯胺-T双相碘标法是细胞因子同位素碘标记的理想方法之一.
The routine iodination methods are easy to lead to biological inactivation of cytokines, which is one of reasons for failure of ligand receptor binding assay. By using two-phase iodination of chromine-T, rhG-CSF and rhEPO were iodinated with Na125I and the characteristic of EPO receptor in BET-2 cell and G-CSF receptor in NFS-60 cell were observed by receptor ligand binding assay. It was showed that the radioactivity of 125I-G-CSF and 125I-EPO were much higher than that obtained by other methods and it was found that there are high and low affinity EPO receptors in BET-2 cells and one high affinity G-CSF receptor in NFS-60 cells. These results are in accord with literature data. It suggests that the two-phase iodination of chromine-T is an ideal method to iodinate cytokines.
从玉文,陈家佩,邵源.蛋白质氯胺-T双相碘标法的建立及其应用[J].生物化学与生物物理进展,1999,26(6):593-596
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