Computer simulation studies of the catalytic mechanism of human aldose reductase

Varnai, Peter and Warshel, Arieh (2000) Computer simulation studies of the catalytic mechanism of human aldose reductase. Journal of American Chemical Society, 122 (16). 3849¿3860. ISSN 00027863

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Aldose reductase, an NADPH dependent oxidoreductase, has received considerable attention due to its possible link to diabetic and galactosemic complications. It is known that the catalytic reaction involves a hydride shift from NADPH and a proton transfer from a suitable proton donor to the carbonyl group of the substrate. However, the details of the process are still unclear. The present work explores the catalytic mechanism of the enzyme by using the semi-microscopic protein dipoles Langevin dipoles (PDLD/S) and the empirical valence bond (EVB) methods. The pKa values of His-110 and Tyr-48 are evaluated to determine which of these two residues donates the proton in the reaction. It is found that the free energy of protonation of His-110 in its protein site is 9 kcal/mol and hence the pKa of this residue is abnormally low. Consequently, His-110 is not protonated in the active site of aldose reductase. On the other hand, it is found that the pKa of Tyr-48 is lowered to 8.5 in the active site due to the stabilization by the unique local environment of the phenol group. We conclude that Tyr-48 acts as the proton donor in the reduction of aldehydes by aldose reductase, while the neutral His-110 has a role in substrate binding during the catalysis. To obtain a quantitative picture of the energetics of different feasible catalytic mechanisms in the protein we follow the EVB philosophy and calibrate the potential surface of the catalytic reaction in a solvent cage by using the relevant energetics from experiments. It is found that a mechanism where a proton transfer precedes the hydride transfer is unfavorable in the solvent cage, relative to the alternative mechanism where the hydride transfer precedes protonation. Furthermore, our study of the reaction in the actual protein environment indicates that an initial proton transfer step would require prohibitively high energy. Thus, the most probable catalytic mechanism commences with the hydride shift, followed by a proton transfer from Tyr-48. The calculations show that in water the activation barrier for the hydride shift is 20 kcal/mol, which is far above the barrier of the subsequent proton transfer. The protein environment stabilizes the transition state of the hydride shift by 3 kcal/mol and destabilizes the intermediate state by 8 kcal/mol relative to the corresponding states in the water cage. This finding is consistent with the physiological role of the enzyme in detoxification where it catalyzes the reduction of a wide range of carbonyl-containing substrates without particular specificity. It is argued that it may be difficult for an enzyme to both satisfy this demand and catalyze the reaction beyond the simple role of bringing the proton and hydride donor groups to the proximity of the substrate.

Item Type: Article
Schools and Departments: School of Life Sciences > Chemistry
Depositing User: Peter Varnai
Date Deposited: 06 Feb 2012 18:45
Last Modified: 19 Mar 2012 14:53
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