posted on 2012-02-14, 00:00authored bySangyun Lee, Ji-Hyun Kim, Sangyoub Lee
Acetylcholinesterase is an enzyme with a very high turnover
rate;
it quenches the neurotransmitter, acetylcholine, at the synapse. We
have investigated the kinetics of the enzyme reaction by calculating
the diffusion rate of the substrate molecule along an active site
channel inside the enzyme from atomic-level molecular dynamics simulations.
In contrast to the previous works, we have found that the internal
substrate diffusion is the determinant of the acetylcholinesterase
kinetics in the low substrate concentration limit. Our estimate of
the overall bimolecular reaction rate constant for the enzyme is in
good agreement with the experimental data. In addition, the present
calculation provides a reasonable explanation for the effects of the
ionic strength of solution and the mutation of surface residues of
the enzyme. The study suggests that internal diffusion of the substrate
could be a key factor in understanding the kinetics of enzymes of
similar characteristics.