Milligan Carol J, Möller Clemens
Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre, Kenneth Myer Building, Royal Parade, Melbourne, VIC, Australia.
Methods Mol Biol. 2013;998:171-87. doi: 10.1007/978-1-62703-351-0_13.
Ion channels are integral membrane proteins that regulate the flow of ions across the plasma membrane and the membranes of intracellular organelles of both excitable and non-excitable cells. Ion channels are vital to a wide variety of biological processes and are prominent components of the nervous system and cardiovascular system, as well as controlling many metabolic functions. Furthermore, ion channels are known to be involved in many disease states and as such have become popular therapeutic targets. For many years now manual patch-clamping has been regarded as one of the best approaches for assaying ion channel function, through direct measurement of ion flow across these membrane proteins. Over the last decade there have been many remarkable breakthroughs in the development of technologies enabling the study of ion channels. One of these breakthroughs is the development of automated planar patch-clamp technology. Automated platforms have demonstrated the ability to generate high-quality data with high throughput capabilities, at great efficiency and reliability. Additional features such as simultaneous intracellular and extracellular perfusion of the cell membrane, current clamp operation, fast compound application, an increasing rate of parallelization, and more recently temperature control have been introduced. Furthermore, in addition to the well-established studies of over-expressed ion channel proteins in cell lines, new generations of planar patch-clamp systems have enabled successful studies of native and primary mammalian cells. This technology is becoming increasingly popular and extensively used both within areas of drug discovery as well as academic research. Many platforms have been developed including NPC-16 Patchliner(®) and SyncroPatch(®) 96 (Nanion Technologies GmbH, Munich), CytoPatch™ (Cytocentrics AG, Rostock), PatchXpress(®) 7000A, IonWorks(®) Quattro and IonWorks Barracuda™, (Molecular Devices, LLC); Dynaflow(®) HT (Cellectricon AB, Mölndal), QPatch HT (Sophion A/S, Copenhagen), IonFlux HT (Fluxion Bioscience Inc, USA), which have demonstrated the capability to generate recordings similar in quality to that of conventional patch clamping. Here we describe features of Nanion's NPC-16 Patchliner(®) and processes and protocols suited for this particularly flexible and successful high-throughput automated platform, which is based on planar patch-clamp technology. However, many of the protocols and notes given in this chapter can be applied to other automated patch-clamp platforms, similarly.
离子通道是整合膜蛋白,可调节离子穿过质膜以及可兴奋细胞和不可兴奋细胞的细胞内细胞器膜的流动。离子通道对多种生物学过程至关重要,是神经系统和心血管系统的重要组成部分,还控制着许多代谢功能。此外,已知离子通道与许多疾病状态有关,因此已成为热门的治疗靶点。多年来,手动膜片钳技术一直被视为通过直接测量离子跨这些膜蛋白的流动来检测离子通道功能的最佳方法之一。在过去十年中,在使离子通道研究成为可能的技术开发方面取得了许多重大突破。其中一项突破是自动平面膜片钳技术的发展。自动化平台已展示出能够以高效率和高可靠性生成具有高通量能力的高质量数据。还引入了其他功能,如细胞膜的细胞内和细胞外同时灌注、电流钳操作、快速化合物应用、并行化率不断提高,以及最近的温度控制。此外,除了对细胞系中过表达的离子通道蛋白进行的成熟研究外,新一代平面膜片钳系统还成功地对天然和原代哺乳动物细胞进行了研究。这项技术在药物发现领域和学术研究中越来越受欢迎且应用广泛。已经开发了许多平台,包括NPC - 16 Patchliner(®)和SyncroPatch(®) 96(德国慕尼黑的Nanion Technologies GmbH公司)、CytoPatch™(德国罗斯托克的Cytocentrics AG公司)、PatchXpress(®) 7000A、IonWorks(®) Quattro和IonWorks Barracuda™(美国Molecular Devices, LLC公司);Dynaflow(®) HT(瑞典Mölndal的Cellectricon AB公司)、QPatch HT(丹麦哥本哈根的Sophion A/S公司)、IonFlux HT(美国Fluxion Bioscience Inc公司),这些平台已证明能够生成与传统膜片钳记录质量相似的记录。在此,我们描述了Nanion公司的NPC - 16 Patchliner(®)的特点以及适用于这个特别灵活且成功的基于平面膜片钳技术的高通量自动化平台的流程和方案。然而,本章给出的许多方案和说明同样可应用于其他自动膜片钳平台。