• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于在自动QPatch-16中评估α7烟碱型乙酰胆碱受体激动剂的自动膜片钳检测方法的开发。

Development of Automated Patch Clamp Assay for Evaluation of α7 Nicotinic Acetylcholine Receptor Agonists in Automated QPatch-16.

作者信息

Hao Yuchen, Tang Jingshu, Wang KeWei

机构信息

1 Department of Molecular and Cellular Pharmacology, State Key Laboratory of Natural and Biomimetic Drugs, Peking University School of Pharmaceutical Sciences , Beijing, China .

出版信息

Assay Drug Dev Technol. 2015 Apr;13(3):174-84. doi: 10.1089/adt.2014.622. Epub 2015 Apr 16.

DOI:10.1089/adt.2014.622
PMID:25880723
Abstract

The α7 nicotinic acetylcholine receptor (α7 nAChR) is an important and challenging target for drug discovery in the area of neuropsychiatric disorders. The current screening for chemicals targeting α7 nAChRs is primarily achieved by the use of low-throughput assay two-electrode voltage clamp (TEVC) in nonmammalian Xenopus oocytes. Automated patch clamp system has emerged as an attractive approach compared to conventional electrophysiology. To develop a mammalian cell-based functional assay in an automated electrophysiology system, we in this study generated a stable expression of α7 nAChRs in GH3 cells that originated from a rat pituitary tumor cell line and utilized automated QPatch-16 to test a set of tool compounds and chemicals identified as α7 agonists by TEVC. For the improvement of evaluating weak or partial α7 nAChRs agonists, we achieved enhancement of the signal-to-noise ratio by the addition of a positive allosteric modulator PNU-120596, which only activates α7 current in the presence of agonist. This improved assay was further validated by using known α7 partial agonists, such as RG3487, EVP-6124, and A-P90. Using this validated assay, we were able to identify a novel agonist 140507C that partially activates α7 nAChRs. Taken together, our results validate the use of QPatch-16 for evaluation α7 partial agonists, demonstrating its utility as an effective tool for α7 ion channel drug discovery.

摘要

α7烟碱型乙酰胆碱受体(α7 nAChR)是神经精神疾病药物研发领域一个重要且具有挑战性的靶点。目前针对α7 nAChRs的化学物质筛选主要通过在非哺乳动物非洲爪蟾卵母细胞中使用低通量双电极电压钳(TEVC)检测来实现。与传统电生理学相比,自动膜片钳系统已成为一种有吸引力的方法。为了在自动电生理系统中开发基于哺乳动物细胞的功能检测方法,我们在本研究中使源自大鼠垂体肿瘤细胞系的GH3细胞稳定表达α7 nAChRs,并利用自动QPatch-16检测一组经TEVC鉴定为α7激动剂的工具化合物和化学物质。为了改进对弱或部分α7 nAChRs激动剂的评估,我们通过添加正变构调节剂PNU-120596提高了信噪比,该调节剂仅在激动剂存在时激活α7电流。使用已知的α7部分激动剂,如RG3487、EVP-6124和A-P90,进一步验证了这种改进的检测方法。使用这种经过验证的检测方法,我们能够鉴定出一种新型激动剂140507C,它能部分激活α7 nAChRs。综上所述,我们的结果验证了使用QPatch-16评估α7部分激动剂的有效性,证明了其作为α7离子通道药物研发有效工具的实用性。

相似文献

1
Development of Automated Patch Clamp Assay for Evaluation of α7 Nicotinic Acetylcholine Receptor Agonists in Automated QPatch-16.用于在自动QPatch-16中评估α7烟碱型乙酰胆碱受体激动剂的自动膜片钳检测方法的开发。
Assay Drug Dev Technol. 2015 Apr;13(3):174-84. doi: 10.1089/adt.2014.622. Epub 2015 Apr 16.
2
Evaluation of alpha7 nicotinic acetylcholine receptor agonists and positive allosteric modulators using the parallel oocyte electrophysiology test station.使用平行卵母细胞电生理测试站评估α7烟碱型乙酰胆碱受体激动剂和正变构调节剂。
Assay Drug Dev Technol. 2009 Aug;7(4):374-90. doi: 10.1089/adt.2009.0194.
3
In vitro pharmacological characterization of a novel selective alpha7 neuronal nicotinic acetylcholine receptor agonist ABT-107.新型选择性 alpha7 型烟碱型乙酰胆碱受体激动剂 ABT-107 的体外药理学特性研究。
J Pharmacol Exp Ther. 2010 Sep 1;334(3):863-74. doi: 10.1124/jpet.110.167072. Epub 2010 May 26.
4
Characterization of compounds on nicotinic acetylcholine receptor alpha7 channels using higher throughput electrophysiology.使用高通量电生理学对烟碱型乙酰胆碱受体α7通道上的化合物进行表征。
J Neurosci Methods. 2009 Feb 15;177(1):142-8. doi: 10.1016/j.jneumeth.2008.10.007. Epub 2008 Oct 19.
5
A novel positive allosteric modulator of the alpha7 neuronal nicotinic acetylcholine receptor: in vitro and in vivo characterization.一种新型α7神经元烟碱型乙酰胆碱受体正向变构调节剂:体外和体内特性研究
J Neurosci. 2005 Apr 27;25(17):4396-405. doi: 10.1523/JNEUROSCI.5269-04.2005.
6
Distinct profiles of alpha7 nAChR positive allosteric modulation revealed by structurally diverse chemotypes.结构多样的化学类型揭示了α7烟碱型乙酰胆碱受体阳性变构调节的不同特征。
Mol Pharmacol. 2007 Sep;72(3):715-24. doi: 10.1124/mol.107.035410. Epub 2007 Jun 12.
7
Electrophysiological investigation of the effect of structurally different bispyridinium non-oxime compounds on human α7-nicotinic acetylcholine receptor activity-An in vitro structure-activity analysis.结构不同的双吡啶𬭩非肟类化合物对人α7-烟碱型乙酰胆碱受体活性的电生理学研究-体外结构-活性分析。
Toxicol Lett. 2018 Sep 1;293:157-166. doi: 10.1016/j.toxlet.2017.11.025. Epub 2017 Nov 27.
8
Synthesis, Pharmacological Characterization, and Structure-Activity Relationships of Noncanonical Selective Agonists for α7 nAChRs.非经典选择性α7 nAChR 激动剂的合成、药理学特征及构效关系。
J Med Chem. 2019 Nov 27;62(22):10376-10390. doi: 10.1021/acs.jmedchem.9b01467. Epub 2019 Nov 19.
9
Competitive binding at a nicotinic receptor transmembrane site of two α7-selective positive allosteric modulators with differing effects on agonist-evoked desensitization.两种 α7 选择性正变构调节剂在烟碱受体跨膜位点的竞争性结合,其对激动剂诱导脱敏的影响不同。
Neuropharmacology. 2011 Dec;61(8):1306-13. doi: 10.1016/j.neuropharm.2011.07.035. Epub 2011 Jul 30.
10
Counteracting desensitization of human α7-nicotinic acetylcholine receptors with bispyridinium compounds as an approach against organophosphorus poisoning.用双吡啶化合物对抗人α7-烟碱型乙酰胆碱受体脱敏作为对抗有机磷中毒的一种方法。
Toxicol Lett. 2018 Sep 1;293:149-156. doi: 10.1016/j.toxlet.2017.12.005. Epub 2017 Dec 14.

引用本文的文献

1
Transfection methods for high-throughput cellular assays of voltage-gated calcium and sodium channels involved in pain.用于高通量细胞测定电压门控钙和钠通道的转染方法与疼痛有关。
PLoS One. 2021 Mar 5;16(3):e0243645. doi: 10.1371/journal.pone.0243645. eCollection 2021.
2
Using automated patch clamp electrophysiology platforms in pain-related ion channel research: insights from industry and academia.利用自动化膜片钳电生理学平台进行痛相关离子通道研究:来自工业界和学术界的见解。
Br J Pharmacol. 2018 Jun;175(12):2312-2321. doi: 10.1111/bph.13916. Epub 2017 Jul 18.
3
Electrophysiology-Based Assays to Detect Subtype-Selective Modulation of Human Nicotinic Acetylcholine Receptors.
基于电生理学的检测方法用于检测人类烟碱型乙酰胆碱受体的亚型选择性调节
Assay Drug Dev Technol. 2016 Aug;14(6):333-44. doi: 10.1089/adt.2015.688.
4
Novel screening techniques for ion channel targeting drugs.用于离子通道靶向药物的新型筛选技术。
Channels (Austin). 2015;9(6):367-75. doi: 10.1080/19336950.2015.1079675. Epub 2015 Nov 10.