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出 处:《标记免疫分析与临床》1999年第4期227-231,共5页Labeled Immunoassays and Clinical Medicine
基 金:卫生部科学研究基金
摘 要:用放射配体结合分析技术建立了125I- CYP测定人外周淋巴细胞β肾上腺素能受体(βAR)的方法, 并进行了系列鉴定。用结合饱和实验、动力学实验及竞争抑制实验来鉴定125I-CYP测定人外周淋巴细胞βAR 的可靠性及实用性。结果证明: 125I- CYP与βAR 的结合符合配体可饱和, 结合与解离迅速, 结构特异性等特征。由于此方法需血量少, 特异性高, 操作方便, 结果可靠, 且所需设备简单, 可以在临床及科研中推广使用。In order to establish and identify the method measuring β-adrenoceptor (βAR) in human peripheral lymphocyte using 125 I-cyanopindolol ( 125 I-CYP) with radioligand binding assay (RLBA), binding assay, kinetic experiments and competitive inhibition analysis were used to measure binding of βAR to 125 I-CYP and to identify it.Binding assay showed that there was a saturable process with 4406±484 receptors/per cell at maximal occupancy of the sites and a high affinity ( K d=37.23±3.62pmol/L, n=22).Kinetic studies showed that 125 I-CYP binding to βAR was rapid and reversible.Analysis of inhibition of 125 I-CYP binding to βAR possessed high specificity.Conclusion: The method used in the present study possessed the advantages of lesser blood sample, easiness to operate and reliability of result, therefore, it might be further popularized in clinical applications.
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