Hanes–Woolf plot

Hanes–Woolf plot

In biochemistry, a Hanes–Woolf plot is a graphical representation of enzyme kinetics in which the ratio of the initial substrate concentration [S] to the reaction velocity v is plotted against [S]. It is based on the rearrangement of the Michaelis–Menten equation shown below:

{[S] \over v}={[S] \over V_{\max }}+{K_{m} \over V_{\max }}

where K_m is the Michaelis–Menten constant and V_max is the maximum reaction velocity.

J B S Haldane stated that this method was due to Barnet Woolf.^[1] It was also used by Charles Samuel Hanes, even though he neither mentions nor cites Woolf.^[2] Hanes pointed out that the use of linear regression to determine kinetic parameters from this type of linear transformation is flawed, because it generates the best fit between observed and calculated values of 1/v, rather than v.

The equation can be derived from the Michaelis–Menten equation as follows:

v={{V_{{\max }}[S]} \over {K_{m}+[S]}}

invert and multiply by [S]:

{[S] \over v}={{[S](K_{m}+[S])} \over {V_{{\max }}[S]}}={{K_{m}+[S]} \over {V_{\max }}}

Rearrange:

{[S] \over v}={1 \over V_{\max }}[S]+{K_{m} \over V_{\max }}

As is clear from the equation, perfect data will yield a straight line of slope 1/V_max, a y-intercept of K_m/V_max and an x-intercept of −K_m.

Like other techniques that linearize the Michaelis–Menten equation, the Hanes–Woolf plot was used historically for rapid determination of the important kinetic parameters K_m, V_max and V_max/K_m, but it has been superseded by nonlinear regression methods that are significantly more accurate and no longer computationally inaccessible. It remains useful, however, as a means to present data graphically.

One drawback of the Hanes–Woolf approach is that neither ordinate nor abscissa represent independent variables: both are dependent on substrate concentration. As a result, the typical measure of goodness of fit, the correlation coefficient R, is not applicable.

References

↑ Haldane, J. B. S. (20 April 1957). "Graphical Methods in Enzyme Chemistry". Nature. 179 (832). doi:10.1038/179832b0.
↑ Hanes, CS (1932). "Studies on plant amylases: The effect of starch concentration upon the velocity of hydrolysis by the amylase of germinated barley.". Biochemical Journal. 26 (5): 1406–1421. PMC 1261052 . PMID 16744959.

Enzymes
Activity	Active site Binding site Catalytic triad Oxyanion hole Enzyme promiscuity Catalytically perfect enzyme Coenzyme Cofactor Enzyme catalysis
Regulation	Allosteric regulation Cooperativity Enzyme inhibitor
Classification	EC number Enzyme superfamily Enzyme family List of enzymes
Kinetics	Enzyme kinetics Eadie–Hofstee diagram Hanes–Woolf plot Lineweaver–Burk plot Michaelis–Menten kinetics
Types	EC1 Oxidoreductases (list) EC2 Transferases (list) EC3 Hydrolases (list) EC4 Lyases (list) EC5 Isomerases (list) EC6 Ligases (list)

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Hanes–Woolf plot

See also

References