Hogg P J, Winzor D J
Biochim Biophys Acta. 1985 Dec 13;843(3):159-63. doi: 10.1016/0304-4165(85)90134-5.
A general counterpart of the Scatchard analysis has been developed which takes into account the valence of the ligand. Its use is first demonstrated by application to binding data obtained by exclusion chromatography of mixtures of Dextran T2000 and concanavalin A (a bivalent ligand) on a column of porous glass beads (Glyceryl-CPG 170) equilibrated at 5 degrees C with phosphate-chloride buffer (pH 5.5), I 0.5. A recycling partition equilibrium study with Sephadex G-100 as gel phase then provides a quantitative evaluation of the interaction between haemoglobin and a monoclonal mouse antihaemoglobin antibody preparation in 0.1 M phosphate (pH 7.0) in order to emphasize the ability of the present analysis to consider collectively binding results obtained with a range of acceptor concentrations. Finally, the use of the generalized Scatchard analysis to assess acceptor site homogeneity is illustrated by reappraisal of results for the binding of glyceraldehyde-3-phosphate dehydrogenase to erythrocyte membranes.
已开发出一种考虑配体价态的Scatchard分析通用对应方法。首先通过将其应用于在5℃下用磷酸盐 - 氯化物缓冲液(pH 5.5)、离子强度0.5平衡的多孔玻璃珠柱(甘油基 - CPG 170)上对葡聚糖T2000和伴刀豆球蛋白A(一种二价配体)混合物进行排阻色谱法获得的结合数据,来证明其用途。然后以葡聚糖凝胶G - 100作为凝胶相进行循环分配平衡研究,对血红蛋白与单克隆小鼠抗血红蛋白抗体制剂在0.1 M磷酸盐(pH 7.0)中的相互作用进行定量评估,以强调本分析能够综合考虑一系列受体浓度下获得的结合结果。最后,通过重新评估甘油醛 - 3 - 磷酸脱氢酶与红细胞膜结合的结果,说明了使用广义Scatchard分析评估受体位点同质性的情况。