Asante-Appiah E, Chan W W
Department of Biochemistry, McMaster University, Hamilton, ON, Canada.
Biochem J. 1996 Nov 15;320 ( Pt 1)(Pt 1):17-26. doi: 10.1042/bj3200017.
The concurrent effects of two enzyme inhibitors have been analysed previously with the Yonetani-Theorell plot to obtain insight into the interactions between bound inhibitors. This procedure, like many other traditional graphical methods in enzymology, is based on the estimation of intersecting tendencies in a family of lines. In a recent paper from this laboratory [Chan (1995) Biochem. J. 311, 981-985] it was shown that a plot of this nature may sometimes be replaced, with advantage, by a 'combination plot' in which all data points are accommodated in a single line. We have now extended this approach to analyse the effects of multiple inhibitors and have developed combination plots which illustrate the interaction behaviour in an optimal manner. Thus, in these plots, the synergistic or antagonistic nature of the interactions is clearly evident from the slope, which also provides a direct estimate of the interaction coefficient. The analysis is more efficient and consequently requires fewer enzyme assays. This approach is applicable to various special cases, including that in which three inhibitors bind simultaneously to the enzyme.
先前已用米氏-泰奥雷尔图分析了两种酶抑制剂的协同效应,以深入了解结合抑制剂之间的相互作用。与酶学中许多其他传统的图形方法一样,该方法基于对一组直线相交趋势的估计。在本实验室最近发表的一篇论文中[陈(1995年)《生物化学杂志》311卷,981 - 985页]表明,这种性质的图有时可以用“组合图”取而代之,这样做有好处,因为在组合图中所有数据点都能容纳在一条直线上。我们现在已经扩展了这种方法来分析多种抑制剂的效应,并开发了能以最佳方式说明相互作用行为的组合图。因此,在这些图中,相互作用的协同或拮抗性质从斜率上清晰可见,斜率还能直接估计相互作用系数。这种分析更高效,因此所需的酶分析次数更少。该方法适用于各种特殊情况,包括三种抑制剂同时与酶结合的情况。