Hanes–Woolf plot

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Hanes–Woolf plot

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

where is the Michaelis constant and is the limiting rate.[1]

J B S Haldane stated, reiterating what he and K. G. Stern had written in their book,[2] that this rearrangement was due to Barnet Woolf.[3] However, it was just one of three transformations introduced by Woolf, who did not use it as the basis of a plot. There is therefore no strong reason for attaching his name to it. It was first published by C. S. Hanes, though he did not use it as plot either.[4] Hanes said 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 , rather than .[5]

Starting from the Michaelis–Menten equation:

we can take reciprocals of both sides of the equation to obtain the equation underlying the Lineweaver–Burk plot:

·

which can be rearranged to express a different straight-line relationship:

which can be rearranged to give

·

Thus in the absence of experimental error data a plot of against yields a straight line of slope , an intercept on the ordinate of and an intercept on the abscissa of .

Like other techniques that linearize the Michaelis–Menten equation, the Hanes–Woolf plot was used historically for rapid determination of the kinetic parameters , and ', but it has been largely superseded by nonlinear regression methods that are significantly more accurate and no longer computationally inaccessible.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.

See also[edit]

References[edit]

  1. ^ The term maximum rate is often used, but not recommended by the IUBMB; see Cornish-Bowden, A (2014). "Current IUBMB recommendations on enzyme nomenclature and kinetics". Persp. Sci. 1: 74–87. doi:10.1016/j.pisc.2014.02.006].
  2. ^ Haldane, J B S; Stern, K G (1932). Allgemeine Chemie der Enzyme. Dresden and Leipzig: Steinkopff. pp. 119–120.
  3. ^ Haldane, J. B. S. (20 April 1957). "Graphical Methods in Enzyme Chemistry". Nature. 179 (832): 832. Bibcode:1957Natur.179R.832H. doi:10.1038/179832b0. S2CID 4162570.
  4. ^ Hanes, CS (1932). "Studies on plant amylases: The effect of starch concentration upon the velocity of hydrolysis by the amylase of germinated barley". Biochem. J. 26 (5): 1406–1421. doi:10.1042/bj0261406. PMC 1261052. PMID 16744959.
  5. ^ Hanes's comment is itself flawed, because deviations in are not proportional to deviations in and do not requiring the same weighting.