Reducing agents facilitate membrane patch seal integrity and longevity.

Channels (Austin, Tex.) Pub Date : 2024-12-01 Epub Date: 2023-12-28 DOI:10.1080/19336950.2023.2297621
Damayantee Das, Anson Wong, Timothy N Friedman, Bradley J Kerr, Harley T Kurata, Shawn M Lamothe
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Abstract

The patch clamp method is a widely applied electrophysiological technique used to understand ion channel activity and cellular excitation. The formation of a high resistance giga-ohm seal is required to obtain high-quality recordings but can be challenging due to variables including operator experience and cell preparation. Therefore, the identification of methods to promote the formation and longevity of giga-ohm seals may be beneficial. In this report, we describe our observation that the application of reducing agents (DTT and TCEP) to the external bath solution during whole-cell patch clamp recordings of heterologous cells (HEK and LM) and cultured primary cells (DRG neurons) enhanced the success of giga-ohm seal formation. Reducing agents also maintained the integrity of the seal for longer periods of time at strong hyperpolarizing voltages, whereas an oxidizing agent (H2O2) appeared to have the opposite effect. In summary, we report a useful tool to improve the quality of patch clamp recordings that may be helpful in certain experimental contexts.

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还原剂可提高膜片密封的完整性和使用寿命。
膜片钳法是一种广泛应用的电生理技术,用于了解离子通道活动和细胞兴奋。要获得高质量的记录,需要形成高电阻千欧密封,但由于操作者的经验和细胞制备等变量,形成千欧密封可能具有挑战性。因此,找出促进千欧密封的形成和延长其寿命的方法可能是有益的。在本报告中,我们描述了对异源细胞(HEK 和 LM)和培养的原代细胞(DRG 神经元)进行全细胞膜片钳记录时,在外部浴液中加入还原剂(DTT 和 TCEP)可提高千欧密封形成的成功率的观察结果。在强超极化电压下,还原剂还能在更长的时间内保持密封的完整性,而氧化剂(H2O2)似乎有相反的效果。总之,我们报告了一种提高膜片钳记录质量的有用工具,在某些实验环境中可能会有所帮助。
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A structural atlas of druggable sites on Nav channels. Sodium currents in naïve mouse dorsal root ganglion neurons: No major differences between sexes. Novel insights into voltage-gated ion channels: Translational breakthroughs in medical oncology. Reducing agents facilitate membrane patch seal integrity and longevity. A phenylalanine at the extracellular side of Kir1.1 facilitates potassium permeation.
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