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In biochemistry, an Eadie–Hofstee diagram (also Woolf–Eadie–Augustinsson–Hofstee or Eadie–Augustinsson plot) is a graphical representation of enzyme kinetics in which reaction rate is plotted as a function of the ratio between rate and substrate concentration: : where ''v'' represents reaction rate, ''Km'' is the Michaelis–Menten constant, () is the substrate concentration, and ''V''max is the maximum reaction rate. It can be derived from the Michaelis–Menten equation as follows: : invert and multiply with : : Rearrange: : Isolate v: : A plot of v against ''v''/() will hence yield ''V''max as the y-intercept, ''V''max/Km as the x-intercept, and ''Km'' as the negative slope. Like other techniques that linearize the Michaelis–Menten equation, the Eadie-Hofstee plot was used historically for rapid identification of important kinetic terms like ''Km'' and ''V''max, but has been superseded by nonlinear regression methods that are significantly more accurate and no longer computationally inaccessible. It is also more robust against error-prone data than the Lineweaver–Burk plot, particularly because it gives equal weight to data points in any range of substrate concentration or reaction rate. (The Lineweaver–Burk plot unevenly weights such points.) Both plots remain useful as a means to present data graphically. One drawback from the Eadie–Hofstee approach is that neither ordinate nor abscissa represent independent variables: both are dependent on reaction rate. Thus any experimental error will be present in both axes. Also, experimental error or uncertainty will propagate unevenly and become larger over the abscissa thereby giving more weight to smaller values of ''v''/(). Therefore, the typical measure of goodness of fit for linear regression, the correlation coefficient ''R'', is not applicable. ==See also== * Michaelis–Menten equation * Lineweaver–Burk plot * Hanes–Woolf plot 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Eadie–Hofstee diagram」の詳細全文を読む スポンサード リンク
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