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Title: A new crystal form of human acetylcholinesterase for exploratory room-temperature crystallography studies

Journal Article · · Chemico-Biological Interactions
ORCiD logo [1];  [2];  [3];  [4];  [2];  [5];  [2]
  1. Univ. of Tennessee, Knoxville, TN (United States)
  2. Univ. of California San Diego, La Jolla, CA (United States)
  3. The Ohio State Univ., Columbus, OH (United States)
  4. Univ. of Utah, Salt Lake City, UT (United States)
  5. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

Structure-guided design of novel pharmacologically active molecules relies at least in part on functionally relevant accuracy of macromolecular structures for template based drug design. Currently, about 95% of all macromolecular X-ray structures available in the PDB (Protein Data Bank) were obtained from diffraction experiments at low, cryogenic temperatures. However, it is known that functionally relevant conformations of both macromolecules and pharmacological ligands can differ at higher, physiological temperatures. We describe in this article development and properties of new human acetylcholinesterase (AChE) crystals of space group P31 and a new unit cell, amenable for room-temperature X-ray diffraction studies. Here, we co-crystallized hAChE in P31 unit cell with the reversible inhibitor 9-aminoacridine that binds at the base of the active center gorge in addition to inhibitors that span the full length of the gorge, donepezil (Aricept, E2020) and AChE specific inhibitor BW284c51. Their new low temperature P31 space group structures appear similar to those previously obtained in the different P3121 unit cell. Successful solution of the new room temperature 3.2 Å resolution structure of BW284c51*hAChE complex from large P31 crystals enables us to proceed with studying room temperature structures of lower affinity complexes, such as oxime reactivators bound to hAChE, where temperature-related conformational diversity could be expected in both oxime and hAChE, which could lead to better informed structure-based design under conditions approaching physiological temperature.

Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1559608
Alternate ID(s):
OSTI ID: 1529996
Journal Information:
Chemico-Biological Interactions, Vol. 309, Issue C; ISSN 0009-2797
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 50 works
Citation information provided by
Web of Science

References (18)

Primary structure of Torpedo californica acetylcholinesterase deduced from its cDNA sequence journal January 1986
Atomic structure of acetylcholinesterase from Torpedo californica: a prototypic acetylcholine-binding protein journal August 1991
Structure of acetylcholinesterase complexed with E2020 (Aricept®): implications for the design of new anti-Alzheimer drugs journal March 1999
The impact of crystallization conditions on structure-based drug design: A case study on the methylene blue/acetylcholinesterase complex: The Impact of Crystallization Conditions on Structure-Based Drug Design journal March 2016
Oxime-assisted Acetylcholinesterase Catalytic Scavengers of Organophosphates That Resist Aging journal July 2011
HKL -3000: the integration of data reduction and structure solution – from diffraction images to an initial model in minutes journal July 2006
Structures of Human Acetylcholinesterase in Complex with Pharmacologically Important Ligands journal October 2012
PHENIX: a comprehensive Python-based system for macromolecular structure solution journal January 2010
MolProbity: all-atom contacts and structure validation for proteins and nucleic acids journal May 2007
Features and development of Coot journal March 2010
Inference of Macromolecular Assemblies from Crystalline State journal September 2007
Three distinct domains in the cholinesterase molecule confer selectivity for acetyl- and butyrylcholinesterase inhibitors journal November 1993
Interaction Kinetics of Reversible Inhibitors and Substrates with Acetylcholinesterase and Its Fasciculin 2 Complex journal February 2001
Donepezil: An Important Prototype to the Design of New Drug Candidates for Alzheimer’s Disease journal January 2014
Biochemical and Histochemical Comparison of Cholinesterases in Normal and Alzheimer Brain Tissues journal August 2010
Quaternary ligand binding to aromatic residues in the active-site gorge of acetylcholinesterase. journal October 1993
Crystal structures of human cholinesterases in complex with huprine W and tacrine: elements of specificity for anti-Alzheimer's drugs targeting acetyl- and butyryl-cholinesterase journal July 2013
Structure of a complex of the potent and specific inhibitor BW284C51 with Torpedo californica acetylcholinesterase journal September 2002

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Chasing ChEs-MAO B Multi-Targeting 4-Aminomethyl-7-Benzyloxy-2H-Chromen-2-ones journal December 2019
Design, Synthesis, Molecular Docking, and Cholinesterase Inhibitory Potential of Phthalimide‐Dithiocarbamate Hybrids as New Agents for Treatment of Alzheimer's Disease journal October 2019