Trehalose Mediated Inhibition of Lactate Dehydrogenase from Rabbit Muscle. the Application of Kramers' Theory in Enzyme Catalysis
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Lactate dehydrogenase (LDH) catalyzes the reduction of pyruvate to lactate by using NADH. LDH kinetics has been proposed to be dependent on the dynamics of a loop over the active site. Kramers%27 theory has been useful in the study of enzyme catalysis dependent on large structural dynamics. In this work, LDH kinetics was studied in the presence of trehalose and at different temperatures. In the absence of trehalose, temperature increase raised exponentially the LDH Vmax and revealed a sigmoid transition of Km toward a low-affinity state similar to protein unfolding. Notably, LDH Vmax diminished when in the presence of trehalose, while pyruvate affinity increased and the temperature-mediated binding site transition was hindered. The effect of trehalose on kcat was viscosity dependent as described by Kramers%27 theory since Vmax correlated inversely with the viscosity of the medium. As a result, activation energy (Ea) for pyruvate reduction was dramatically increased by trehalose presence. This work provides experimental evidence that the dynamics of a structural component in LDH is essential for catalysis, i.e., the closing of the loop on the active site. While the trehalose mediated-increased of pyruvate affinity is proposed to be due to the compaction and/or increase of structural order at the binding site. © 2018 American Chemical Society.
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Lactate dehydrogenase (LDH) catalyzes the reduction of pyruvate to lactate by using NADH. LDH kinetics has been proposed to be dependent on the dynamics of a loop over the active site. Kramers' theory has been useful in the study of enzyme catalysis dependent on large structural dynamics. In this work, LDH kinetics was studied in the presence of trehalose and at different temperatures. In the absence of trehalose, temperature increase raised exponentially the LDH Vmax and revealed a sigmoid transition of Km toward a low-affinity state similar to protein unfolding. Notably, LDH Vmax diminished when in the presence of trehalose, while pyruvate affinity increased and the temperature-mediated binding site transition was hindered. The effect of trehalose on kcat was viscosity dependent as described by Kramers' theory since Vmax correlated inversely with the viscosity of the medium. As a result, activation energy (Ea) for pyruvate reduction was dramatically increased by trehalose presence. This work provides experimental evidence that the dynamics of a structural component in LDH is essential for catalysis, i.e., the closing of the loop on the active site. While the trehalose mediated-increased of pyruvate affinity is proposed to be due to the compaction and/or increase of structural order at the binding site. © 2018 American Chemical Society.
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Activation energy; Binding energy; Dynamics; Enzymes; Structural dynamics; Viscosity; Activation energies (Ea); Enzyme catalysis; Experimental evidence; Lactate dehydrogenase; Protein unfolding; Structural component; Structural ordering; Temperature increase; Catalysis; enzyme inhibitor; lactate dehydrogenase; trehalose; animal; antagonists and inhibitors; biocatalysis; chemistry; drug effect; enzymology; Leporidae; metabolism; molecular dynamics; skeletal muscle; Animals; Biocatalysis; Enzyme Inhibitors; L-Lactate Dehydrogenase; Molecular Dynamics Simulation; Muscle, Skeletal; Rabbits; Trehalose
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