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MS Binding Assays with UNC0642 as reporter ligand for the MB327 binding site of the nicotinic acetylcholine receptor.
Nitsche, Valentin; Höfner, Georg; Kaiser, Jesko; Gertzen, Christoph G W; Seeger, Thomas; Niessen, Karin V; Steinritz, Dirk; Worek, Franz; Gohlke, Holger; Paintner, Franz F; Wanner, Klaus T.
Afiliação
  • Nitsche V; Department of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Höfner G; Department of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Kaiser J; Institute for Pharmaceutical and Medicinal Chemistry, Heinrich Heine Universität Düsseldorf, Düsseldorf, Germany.
  • Gertzen CGW; Institute for Pharmaceutical and Medicinal Chemistry, Heinrich Heine Universität Düsseldorf, Düsseldorf, Germany.
  • Seeger T; Bundeswehr Institute of Pharmacology and Toxicology, Munich, Germany.
  • Niessen KV; Bundeswehr Institute of Pharmacology and Toxicology, Munich, Germany.
  • Steinritz D; Bundeswehr Institute of Pharmacology and Toxicology, Munich, Germany.
  • Worek F; Bundeswehr Institute of Pharmacology and Toxicology, Munich, Germany.
  • Gohlke H; Institute for Pharmaceutical and Medicinal Chemistry, Heinrich Heine Universität Düsseldorf, Düsseldorf, Germany; Institute of Bio, and Geosciences (IBG-4: Bioinformatics), Forschungszentrum Jülich, Jülich, Germany.
  • Paintner FF; Department of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, Munich, Germany.
  • Wanner KT; Department of Pharmacy - Center for Drug Research, Ludwig-Maximilians-Universität München, Munich, Germany. Electronic address: klaus.wanner@cup.uni-muenchen.de.
Toxicol Lett ; 392: 94-106, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38216073
ABSTRACT
Intoxications with organophosphorus compounds (OPCs) based chemical warfare agents and insecticides may result in a detrimental overstimulation of muscarinic and nicotinic acetylcholine receptors evolving into a cholinergic crisis leading to death due to respiratory failure. In the case of the nicotinic acetylcholine receptor (nAChR), overstimulation leads to a desensitization of the receptor, which cannot be pharmacologically treated so far. Still, compounds interacting with the MB327 binding site of the nAChR like the bispyridinium salt MB327 have been found to re-establish the functional activity of the desensitized receptor. Only recently, a series of quinazoline derivatives with UNC0642 as one of the most prominent representatives has been identified to address the MB327 binding site of the nAChR, as well. In this study, UNC0642 has been utilized as a reporter ligand to establish new Binding Assays for this target. These assays follow the concept of MS Binding Assays for which by assessing the amount of bound reporter ligand by mass spectrometry no radiolabeled material is required. According to the results of the performed MS Binding Assays comprising saturation and competition experiments it can be concluded, that UNC0642 used as a reporter ligand addresses the MB327 binding site of the Torpedo-nAChR. This is further supported by the outcome of ex vivo studies carried out with poisoned rat diaphragm muscles as well as by in silico studies predicting the binding mode of UNC0646, an analog of UNC0642 with the highest binding affinity, in the recently proposed binding site of MB327 (MB327-PAM-1). With UNC0642 addressing the MB327 binding site of the Torpedo-nAChR, this and related quinazoline derivatives represent a promising starting point for the development of novel ligands of the nAChR as antidotes for the treatment of intoxications with organophosphorus compounds. Further, the new MS Binding Assays are a potent alternative to established assays and of particular value, as they do not require the use of radiolabeled material and are based on a commercially available compound as reporter ligand, UNC0642, exhibiting one of the highest binding affinities for the MB327 binding site known so far.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos de Piridínio / Receptores Nicotínicos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Toxicol Lett Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Compostos de Piridínio / Receptores Nicotínicos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Toxicol Lett Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Holanda