Tailoring Drug Development in the Cholinergic Nervous System through Structural Templates Three targets: Nicotinic Acetylcholine Receptors (nAChR) ~15 subunits in various pentameric permutations Acetylcholinesterase (AChE) Alternatively spliced single gene Neuroligin and Neurexin Synaptic adhesion molecules in situ, Click-Chemistry Leads to Drug Candidates (1) in situ Azide-Alkyne Cycloaddition on WT AChBPs (2) in situ Azide-Alkyne Cycloaddition on MT AChBPs Triazole Regioisomer Identification Cu++/Ru++ catalyzed lead synthesis in microarray AChBP Binding Assay (SPA), Kd X-Ray Structure with AChBPs Whole Cell Binding Assay with nAChRS (SPA), Kd Concentration dependence functional responses Interaction Energy with crystallographic model Binding poses, potential interacting residues Receptor Subtype Occupation Receptor Selectivity Agonism (EC50) or Antagonism (KA) H3-Radioligand Novel Drug Discovery & Development • Synthesis by in situ freeze-frame, click chemistry • Physical analysis of lead complexes (binding energy, conformational changes, X-ray crystallography) • Catalytic synthesis at the milligram level (refinement of SAR is done in microarrays and only leads are taken forward). • Quantitate affinity and activity in vitro • Assay cellular toxicity and efficacy • Efficacy in intact animals • Pharmacokinetic studies of disposition in the target tissues (CNS) and plasma Mechanism and Therapeutic Indications Acetylcholinesterase • Mechanism Antidotal Action at CNS and skeletal muscle targets Scavenging in environment, portals of entry & circulation • Therapeutic Indications Organophosphate pesticide toxicity Nerve agents in terrorism Nicotinic Acetylcholine Receptor • Mechanism Agonist, Partial Agonist and Antagonist Activity at nAChRs. Allosteric Modifiers at nAChRs • Therapeutic Indications Disorders of nervous system development & aging dementias Tobacco cessation Click Chemistry TSRI K. Barry Sharpless* Valery Fokin* Rakesh Sit* Timo Weide Joseph Fotsing Neil Grimster M.G. Finn, Georgia Tech* Kasia Kaczanowska* Gabi Amitai (IIBR) Acetylcholine Binding Protein Scott Hansen Todd Talley Ryan Hibbs Zoran Radic’* Ákos Nemecz* John Yamauchi* Nan Arunrungvichian* Bill Chen* AChE and AChBP Crystal Structures Scott Hansen Ryan Hibbs Todd Talley Akos Nemecz Kasia Kaczanowska* Zoran Radic’* Jean-Pierre Changeux* Pascale Marchot (Marseille)* Yves Bourne (Marseille)* Andy McCammon(UCSD) Jon Lindstrom (Penn) Michal Harel (Weizmann)* David Johnson (UC, Riverside) Steve Sine (Mayo, Rochester) Pharmacokinetics John Casida (UC, Berkeley) & Disposition Zoran Radic* Jordi Molgo (Gif-sur-Yvette) Jeremiah Momper* Mike McIntosh (Univ. of Utah) Edmund Capparelli* Toto Olivera (Univ. of Utah) Manjunatha Kini (NUS) Active center gorge Peripheral site Active center CNS O H 3C P O F CH 3 CH 3 O + A C h E -O H A C h E -O P O CH 3 CH 3 CH 3 Blood-Brain Barrier O P O H 3C F CH 3 CH 3 O + A C h E -O H A C h E -O P O CH 3 Plasma CH 3 CH 3 O + R N OH R N- O P O CH 3 CH 3 CH 3 + A C h E -O H Reactivation of native peripheral AChE Oxime-assisted Catalytic OP hydrolysis in Plasma Alveolar Membrane Site of Exposure O H 3C P O F CH 3 CH 3 CNS O H 3C P O F CH 3 CH 3 O + A C h E -O H A C h E -O P O CH 3 CH 3 CH 3 O P O H 3C F CH 3 CH 3 O + A C h E -O H A C h E -O P O CH 3 x Blood-Brain Barrier Plasma CH 3 CH 3 HON N Reactivation of native peripheral AChE Oxime-assisted Catalytic OP hydrolysis in Plasma Alveolar Membrane Site of Exposure O H 3C P O F CH 3 CH 3 CH O O P O H 3C F CH 3 CH 3 O + A C h E -O H CH 3 P P O CH A C h E -O OH3 CHR3 N R N- O O CH 3 CH + ACh E -O H CNS 3 3 N RR ' N RR 'H + HON HON HN H+ + HN O O x Oxime Reactivation of native AChE in CNS Blood-Brain Barrier Plasma N RR ' O H 3C P O F CH 3 CH 3 O + A C h E -O H P O A C h E -O CH 3 CH 3 CH 3 N RR 'H HON HON H+ HN + HN O O Reactivation of native peripheral AChE Oxime-assisted Catalytic OP hydrolysis in Plasma Alveolar Membrane Site of Exposure O H 3C P O F CH 3 CH 3 AChBP: a structural surrogate of the nAChR Ligand Binding Domain 5 subunits each of which have: I. A large extra cellular domain II. 4 membrane-spanning regions III. α β combinations make up most neuronal receptors Hansen, S. et. al. 2005 Brejc, K. et. al. 2001 Nicotine Anabaseine Cytisine DMXBA Epibatidine Anatoxin-a d-Tubocurarine MLA SPX GYM Lobeline a-Conotoxin Tropisetron Waglerin Sazetidine A a-cobratoxin Granisetron