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Acetylcholine and Acetylcholine Receptors: Textbook Knowledge and New Data

机译:乙酰胆碱和乙酰胆碱受体:教科书知识和新数据

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摘要

It was a pleasure to receive a proposal to organize and be a guest editor of a Special Issue of This is the field in which I am working and personally know some of the leading scientists. My narrow field is the research on the peptide and protein neurotoxins from animal venoms and their application as sophisticated tools for analysis of nicotinic acetylcholine receptors (nAChRs). Recently, together with my colleagues from several European laboratories, I was a guest editor for the Special Issue of devoted to diverse neurotoxins acting on various ligand-gated or voltage-gated ion channels. In this Special Issue, it was decided to focus mostly on the nAChRs. The word “acetylcholine” in the title of the issue is due to the interest in the mechanism of action of this naturally-occurring agonist and also in other endogenous or synthetic compounds regulating nAChR functions and having the potential to lead to novel drugs. Since there are examples where a compound acts on different targets, like galanthamine which inhibits acetylcholinestrase, but is a positive allosteric modulator of the α7 nAChR, or some non-conventional snake venom neurotoxins interacting with both nAChRs and with muscarinic receptors, we decided to cover, although with less detail, muscarinic acetylcholine receptors.
机译:很高兴收到组织和担任《特刊》特约编辑的建议,这是我正在研究的领域,并且我自己认识一些领先的科学家。我的狭窄领域是研究动物毒液中的肽和蛋白质神经毒素及其作为分析烟碱乙酰胆碱受体(nAChRs)的先进工具的应用。最近,我与来自几个欧洲实验室的同事一起,作为特刊的特约编辑,专门研究作用于各种配体门控或电压门控离子通道的多种神经毒素。在本期特刊中,决定主要关注nAChR。问题标题中的“乙酰胆碱”一词是由于对该天然激动剂的作用机理以及对调节nAChR功能并具有导致新药潜力的其他内源性或合成化合物的兴趣。由于存在化合物对不同靶标起作用的例子,例如加兰他敏抑制乙酰胆碱酯酶,但它是α7nAChR的正变构调节剂,或与nAChR和毒蕈碱受体相互作用的某些非常规蛇毒神经毒素,因此我们决定涵盖毒蕈碱型乙酰胆碱受体,尽管细节较少。

著录项

  • 期刊名称 Biomolecules
  • 作者

    Victor I. Tsetlin;

  • 作者单位
  • 年(卷),期 2020(10),6
  • 年度 2020
  • 页码 -1
  • 总页数 3
  • 原文格式 PDF
  • 正文语种
  • 中图分类 生物学;
  • 关键词

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