AChE inhibitors and substrates (Part II)

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Revision as of 12:41, 25 June 2009

AChE monovalent inhibitors (continuation of the page AChE inhibitors and substrates)

6) Edrophonium (EDR) (2ack) is stacked between the aromatic rings of , near the TcAChE which consists of S200, E327, and H440.

7) Rivastigmine (Exelon) is a carbamate inhibitor of AChE, and it is currenly used in therapy of Alzheimer's disease. Rivastigmine (colored yellow) interacts with TcAChE (colored lime) at the . The carbamyl moiety of rivastigmine is to the active-site S200 Oγ. The second part of rivastigmine (the leaving group), NAP ((−)-S-3-[1-(dimethylamino)ethyl]phenol) is also held in the active-site gorge, but it is from the carbamyl moiety, hence, carbamylation took place. The of TcAChE/NAP (colored magenta) is known (1gqs). The TcAChE active-site residues which are interacting with NAP are colored violet. NAP is located in a similar region of TcAChE active site, but with different orientation than that of the NAP part (colored yellow) in the TcAChE/rivastigmine complex. Only H440 and F330 significantly change their side-chain conformations. of the TcAChE active sites in 4 different structures (TcAChE/rivastigmine, TcAChE/NAP, native TcAChE(2ace), and TcAChE/VX (1vxr, TcAChE colored white and VX black)) reveals that the conformation of H440 in the TcAChE/NAP structure is very similar its conformation in the native TcAChE (2ace), but the distance between H440 Nδ and E327 Oε is significantly longer in the TcAChE/rivastigmine and the TcAChE/VX complexes. This structural change disrupts the catalytic triad consisting of S200, E327, H440. This could explain the very slow kinetics of AChE reactivation after its inhibition by rivastigmine.

8) The TcAChE active site consists of two binding subsites. One of them is the "catalytic anionic site" (CAS), which involves the catalytic triad (colored orange) and the conserved residues which also participate in ligand recognition. Another conserved residue (colored cyan) is situated at the second binding subsite, termed the "peripheral anionic site" (PAS), ~14 Å from CAS. is a good example of the PAS-binding AChE inhibitors. of the crystal structure of the edrophonium /TcAChE (mentioned above as a CAS-binding inhibitor) (2ack) on the thioflavin T /TcAChE complex structure (2j3q) shows that these ligands' positions do not overlap. Of note is that Phe330, which is part of the CAS, is the single residue interacting with thioflavin T. This residue is the only one which significantly to avoid clashes in comparison to other CAS residues of the edrophonium /TcAChE complex.

9) Organophosphorus acid anhydride (OP) nerve agents are potent inhibitors which rapidly phosphonylate AChE and then may undergo an internal dealkylation reaction (called "aging") to produce an OP-enzyme conjugate that cannot be reactivated.

Reaction between Ser200OG and Soman, assuming an in-line attack by the OG, followed by spontaneous dealkylation of the O-pinacolyl group.

To understand the basis for irreversible inhibition, we solved the structure of the aged conjugate obtained by reaction of Torpedo californica AChE (TcAChE) with O-pinacolylmethylphosphonofluoridate (soman) by X-ray crystallography to 2.2Å resolution. The highest positive difference density peak corresponded to the OP phosphorus and was located within covalent bonding distance of the active-site serine (S200). The are within hydrogen-bonding distance of four potential donors from catalytic subsites of the enzyme, suggesting that electrostatic forces significantly stabilize the aged enzyme. The methyl group of soman occupies the , bounded by Trp233, Phe288, and Phe290. The active sites of aged sarin-TcAChE (1cfj) and soman-TcAChE were essentially identical and provided structural models for the negatively charged, tetrahedral intermediate that occurs during deacylation with the natural substrate, acetylcholine.

10) is a nonhydrolyzable substrate analogue of AChE. Its hydrolysis is impossible as OTMA possesses atom instead of the in the AChE natural substrate ACh. Similarly to ACh, OTMA covalently binds to the TcAChE (2vja) Oγ at the CAS. At this subsite OTMA also interacts with (cation-π interactions); (electrostatic interaction); (hydrogen bonds). OTMA binds not only at CAS, but also at PAS. A second OTMA molecule interacts with (cation-π interactions), and (weak hydrogen bond). Thus, this dual binding mode of OTMA with TcAChE (to CAS and PAS) could be prototypical for AChE bivalent inhibitors.

Please see also our pages AChE bivalent inhibitors and AChE bivalent inhibitors (Part II).

Selected 3D Structures of AChE

• 2ace This is the original solved structure for Torpedo Californica
• 1ea5 This is one of the highest quality representative X-ray structures in the PDB.
• 1eve The E2020 (Aricept) complex.
• 1ax9 Endrophonium complex.
• 1vot Complex with Huperzine, a Chinese folk medicine.
• 1fss Complex with snake venum toxin Fasciculin-II.
• 1acj Complex with tacrine.
• 1e66 Complex with huprine X.
• 1dx6 Complex with galanthamine.
• 1w6r Complex with galanthamine iminium derivative.
• 2ack Complex with edrophonium.
• 1vzj Structure of the tetramerization domain of acetylcholinesterase.
• 1gqr Complex with rivastigmine.
• 1gqs Complex with NAP alone.
• 1vxr Complex with VX.
• 2vja Complex with OTMA.

References

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