The novel nonapeptide acein targets angiotensin converting enzyme in the brain and induces dopamine release

新型九肽乙酰辅酶 A 靶向大脑中的血管紧张素转换酶并诱导多巴胺释放

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作者:Jérémie Neasta, Charlène Valmalle, Anne-Claire Coyne, Eric Carnazzi, Gilles Subra, Jean-Claude Galleyrand, Didier Gagne, Céline M'Kadmi, Nicole Bernad, Gilbert Bergé, Sonia Cantel, Philippe Marin, Jacky Marie, Jean-Louis Banères, Marie-Lou Kemel, Valérie Daugé, Karine Puget, Jean Martinez

Background and purpose

Using an in-house bioinformatics programme, we identified and synthesized a novel nonapeptide, H-Pro-Pro-Thr-Thr-Thr-Lys-Phe-Ala-Ala-OH. Here, we have studied its biological activity, in vitro and in vivo, and have identified its target in the brain. Experimental approach: The affinity of the peptide was characterized using purified whole brain and striatal membranes from guinea pigs and rats . Its effect on behaviour in rats following intra-striatal injection of the peptide was investigated. A photoaffinity UV cross-linking approach combined with subsequent affinity purification of the ligand covalently bound to its receptor allowed identification of its target. Key

Purpose

Using an in-house bioinformatics programme, we identified and synthesized a novel nonapeptide, H-Pro-Pro-Thr-Thr-Thr-Lys-Phe-Ala-Ala-OH. Here, we have studied its biological activity, in vitro and in vivo, and have identified its target in the brain. Experimental approach: The affinity of the peptide was characterized using purified whole brain and striatal membranes from guinea pigs and rats . Its effect on behaviour in rats following intra-striatal injection of the peptide was investigated. A photoaffinity UV cross-linking approach combined with subsequent affinity purification of the ligand covalently bound to its receptor allowed identification of its target. Key

Results

The peptide bound with high affinity to a single class of binding sites, specifically localized in the striatum and substantia nigra of brains from guinea pigs and rats. When injected within the striatum of rats, the peptide stimulated in vitro and in vivo dopamine release and induced dopamine-like motor effects. We purified the target of the peptide, a ~151 kDa protein that was identified by MS/MS as angiotensin converting enzyme (ACE I). Therefore, we decided to name the peptide acein.

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