The role of Li+, Na+, and K+ in the ligand binding inside the human acetylcholinesterase gorge

Alkali cations can affect the catalytic efficiency of enzymes. This is particularly true when dealing with enzymes whose substrate bears a formal positive charge. Computational and biochemical approaches have been combined to shed light on the atomic aspects of the role of Li+, Na+, and K+ on human acetylcholinesterase (hAChE) ligand binding. In this respect, molecular dynamics simulations and our recently developed metadynamics method were applied to study the entrance of the three cations in the gorge of hAChE, and their effect on the dynamical motion of a ligand (tetramethylammonium) from the bulk of the solvent into the deep narrow enzyme gorge. Furthermore, in order to support the theoretical results, KM and kcat for the acetylcholine hydrolysis in the presence of the three cations were evaluated by using an approach based on the Ellman's method. The combination of computational and biochemical experiments clearly showed that Li+, Na+, and K+ may influence the ligand binding at the hAChE gorge. Proteins 2008. © 2007 Wiley‐Liss, Inc.

[1]  U. P. Fringeli,et al.  Activation of acetylcholinesterase by monovalent (Na+,K+) and divalent (Ca2+,Mg2+) cations. , 1984, Biochemistry.

[2]  J Andrew McCammon,et al.  Role of the catalytic triad and oxyanion hole in acetylcholinesterase catalysis: an ab initio QM/MM study. , 2002, Journal of the American Chemical Society.

[3]  N. Ariel,et al.  Structures of recombinant native and E202Q mutant human acetylcholinesterase complexed with the snake-venom toxin fasciculin-II. , 2000, Acta crystallographica. Section D, Biological crystallography.

[4]  Maurizio Recanatini,et al.  A computational study of the binding of propidium to the peripheral anionic site of human acetylcholinesterase. , 2004, Journal of medicinal chemistry.

[5]  M. Carrillo-Tripp,et al.  A Theoretical Study of the Hydration of Li+ by Monte Carlo Simulations with Refined Ab Initio Based Model Potentials , 2006 .

[6]  Piero Procacci,et al.  ORAC: A Molecular dynamics program to simulate complex molecular systems with realistic electrostatic interactions , 1997 .

[7]  A. Laio,et al.  Flexible docking in solution using metadynamics. , 2005, Journal of the American Chemical Society.

[8]  P Taylor,et al.  Rapid binding of a cationic active site inhibitor to wild type and mutant mouse acetylcholinesterase: Brownian dynamics simulation including diffusion in the active site gorge. , 1998, Biopolymers.

[9]  C. Bartolucci,et al.  "Back door" opening implied by the crystal structure of a carbamoylated acetylcholinesterase. , 1999, Biochemistry.

[10]  J. Mccammon,et al.  Electrostatic Influence on the Kinetics of Ligand Binding to Acetylcholinesterase , 1997, The Journal of Biological Chemistry.

[11]  P. Goodford A computational procedure for determining energetically favorable binding sites on biologically important macromolecules. , 1985, Journal of medicinal chemistry.

[12]  W. L. Jorgensen,et al.  Comparison of simple potential functions for simulating liquid water , 1983 .

[13]  Francesco Luigi Gervasio,et al.  The role of the peripheral anionic site and cation-pi interactions in the ligand penetration of the human AChE gorge. , 2005, Journal of the American Chemical Society.

[14]  D. Quinn,et al.  Acetylcholinesterase: enzyme structure, reaction dynamics, and virtual transition states , 1987 .

[15]  P. Kollman,et al.  A Second Generation Force Field for the Simulation of Proteins, Nucleic Acids, and Organic Molecules , 1995 .

[16]  A. Laio,et al.  Escaping free-energy minima , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[17]  A. Laio,et al.  Assessing the accuracy of metadynamics. , 2005, The journal of physical chemistry. B.

[18]  Ettore Novellino,et al.  Specific targeting of acetylcholinesterase and butyrylcholinesterase recognition sites. Rational design of novel, selective, and highly potent cholinesterase inhibitors. , 2003, Journal of medicinal chemistry.

[19]  K. Courtney,et al.  A new and rapid colorimetric determination of acetylcholinesterase activity. , 1961, Biochemical pharmacology.

[20]  Richard H. Henchman,et al.  The dynamics of ligand barrier crossing inside the acetylcholinesterase gorge. , 2003, Biophysical journal.

[21]  Alessandro Laio,et al.  Efficient exploration of reactive potential energy surfaces using Car-Parrinello molecular dynamics. , 2003, Physical review letters.