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METHOD FOR DETERMINING INTRINSIC BINDING PARAMETERS OF AN ANALYTE TO A LIGAND, A METHOD FOR SELECTING AN ANALYTE FROM A GROUP OF ANALYTS, THE SELECTED LIGAND OR ANALYTE, AND SENSOR
METHOD FOR DETERMINING INTRINSIC BINDING PARAMETERS OF AN ANALYTE TO A LIGAND, A METHOD FOR SELECTING AN ANALYTE FROM A GROUP OF ANALYTS, THE SELECTED LIGAND OR ANALYTE, AND SENSOR
The present invention relates to a method for determining intrinsic binding parameters, such as KD, kd and ka, of an analyte to a ligand, such as a drug and a protein, a drug and a receptor, and an antibody and antigen, wherein the maximal binding response Rmax or RL and at least one binding parameter is determined at at least two different ligand surface densities present on a sensor support, and extrapolating the value of the binding parameter to ligand density = 0, characterized by Rmax=0 or R1=0, to a method of selecting an analyte and/or ligand, and to the selected ligand, analyte and a sensor.
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机译:本发明涉及一种确定内在结合参数的方法,例如K D Sub>,k d Sub>和k a Sub>。配体,例如药物和蛋白质,药物和受体以及抗体和抗原,其中最大结合反应为R max Sub>或R L Sub>和至少一个至少在传感器支持物上存在的两个不同的配体表面密度下确定结合参数,并将结合参数的值外推至配体密度= 0,其特征为Rmax = 0或R 1 Sub> = 0,本发明涉及选择分析物和/或配体的方法,以及选择的配体,分析物和传感器。
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