Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark; Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
Biophys J. 2024 Jul 16;123(14):2122-2135. doi: 10.1016/j.bpj.2024.03.038. Epub 2024 Mar 28.
Acid-sensing ion channels (ASICs) are proton-gated cation channels that contribute to fast synaptic transmission and have roles in fear conditioning and nociception. Apart from activation at low pH, ASIC1a also undergoes several types of desensitization, including acute desensitization, which terminates activation; steady-state desensitization, which occurs at sub-activating proton concentrations and limits subsequent activation; and tachyphylaxis, which results in a progressive decrease in response during a series of activations. Structural insights from a desensitized state of ASIC1 have provided great spatial detail, but dynamic insights into conformational changes in different desensitizing conditions are largely missing. Here, we use electrophysiology and voltage-clamp fluorometry to follow the functional changes of the pore along with conformational changes at several positions in the extracellular and upper transmembrane domain via cysteine-labeled fluorophores. Acute desensitization terminates activation in wild type, but introducing an N414K mutation in the β11-12 linker of mouse ASIC1a interfered with this process. The mutation also affected steady-state desensitization and led to pronounced tachyphylaxis. Although the extracellular domain of this mutant remained sensitive to pH and underwent pH-dependent conformational changes, these conformational changes did not necessarily lead to desensitization. N414K-containing channels also remained sensitive to a known peptide modulator that increases steady-state desensitization, indicating that the mutation only reduced, but not precluded, desensitization. Together, this study contributes to our understanding of the fundamental properties of ASIC1a desensitization, emphasizing the complex interplay between the conformational changes of the extracellular domain and the pore during channel activation and desensitization.
酸敏离子通道(ASICs)是质子门控阳离子通道,有助于快速突触传递,并在恐惧条件反射和痛觉感受中发挥作用。除了在低 pH 值下激活外,ASIC1a 还经历几种类型的脱敏,包括急性脱敏,其终止激活;稳态脱敏,其在亚激活质子浓度下发生并限制随后的激活;以及脱敏,其导致在一系列激活过程中响应逐渐减少。来自 ASIC1 脱敏状态的结构见解提供了很大的空间细节,但对不同脱敏条件下构象变化的动态见解在很大程度上仍然缺失。在这里,我们使用电生理学和电压钳荧光法来跟踪孔的功能变化,以及通过半胱氨酸标记荧光团在外周和上跨膜域的几个位置的构象变化。急性脱敏在野生型中终止激活,但在小鼠 ASIC1a 的β11-12 接头中引入 N414K 突变会干扰此过程。该突变还影响稳态脱敏并导致明显的脱敏。尽管该突变体的细胞外结构域仍然对 pH 敏感并经历 pH 依赖性构象变化,但这些构象变化不一定导致脱敏。含有 N414K 的通道仍然对已知的肽调节剂敏感,该调节剂增加了稳态脱敏,表明该突变仅降低但不排除脱敏。总之,这项研究有助于我们理解 ASIC1a 脱敏的基本特性,强调了在通道激活和脱敏过程中细胞外结构域和孔的构象变化之间的复杂相互作用。