Gupta Smriti, Chiu Yu-Hsin, Manjegowda Mohan C, Desai Bimal N, Ravichandran Kodi S, Bayliss Douglas A
Department of Pharmacology, University of Virginia, School of Medicine, Charlottesville, VA, USA.
Institute of Biotechnology, National Tsing Hua University , Hsinchu, Taiwan.
J Gen Physiol. 2025 Jan 6;157(1). doi: 10.1085/jgp.202413676. Epub 2024 Dec 20.
Pannexin 1 (PANX1) is a member of a topologically related and stoichiometrically diverse family of large pore membrane ion channels that support the flux of signaling metabolites (e.g., ATP) and fluorescent dyes. High-resolution structural analyses have identified PANX1 as a heptamer despite early evidence suggesting that it might be a hexamer. To determine if PANX1 channel activity is supported in both hexameric and heptameric conformations, we examined properties of concatenated PANX1 constructs comprising either six or seven subunits with intact or truncated C-termini (the latter to mimic caspase-cleavage activation). In whole-cell recordings from PANX1-deleted cells, the C-tail-truncated hexameric and heptameric concatemers generated outwardly rectifying PANX1-like currents only after severing the intersubunit linkers. Surprisingly, α1D adrenoceptor stimulation activated constructs with intact or truncated C-tails, even without linker cleavage. In inside-out patches from PANX1-deleted cells, linker cleavage activated C-tail truncated channels derived from either hexameric or heptameric concatemers. The heptamers presented peak unitary conductance and mean open time that was similar to channels assembled from the expression of unlinked single PANX1 subunits and greater than from the hexamers. In addition, the linker-cleaved heptameric concatemers supported greater PANX1-dependent ATP release and TO-PRO-3 uptake than the corresponding hexamers. These data indicate that functional PANX1 channels can be obtained in either hexameric or heptameric conformations and suggest that the distinct unitary properties of heptameric channels are more conducive to large molecule permeation by PANX1; they also suggest that there are distinct structural requirements for C-tail cleavage and receptor-mediated PANX1 activation mechanisms.
泛连接蛋白1(PANX1)是一类拓扑结构相关且化学计量多样的大孔膜离子通道家族的成员,这些通道支持信号代谢物(如ATP)和荧光染料的通量。尽管早期证据表明PANX1可能是六聚体,但高分辨率结构分析已确定其为七聚体。为了确定PANX1通道活性在六聚体和七聚体构象中是否均得到支持,我们研究了由六个或七个亚基组成的串联PANX1构建体的特性,这些亚基具有完整或截短的C末端(后者用于模拟半胱天冬酶切割激活)。在来自缺失PANX1细胞的全细胞记录中,C末端截短的六聚体和七聚体串联体仅在切断亚基间连接子后才产生外向整流的PANX1样电流。令人惊讶的是,α1D肾上腺素能受体刺激即使在没有连接子切割的情况下也能激活具有完整或截短C末端的构建体。在来自缺失PANX1细胞的内向外膜片记录中,连接子切割激活了源自六聚体或七聚体串联体的C末端截短通道。七聚体呈现出的峰值单通道电导和平均开放时间与由未连接的单个PANX1亚基表达组装而成的通道相似,且大于六聚体通道。此外,连接子切割后的七聚体串联体比相应的六聚体支持更大的PANX1依赖性ATP释放和TO-PRO-3摄取。这些数据表明功能性PANX1通道可以以六聚体或七聚体构象获得,并表明七聚体通道独特的单通道特性更有利于PANX1对大分子的通透;它们还表明C末端切割和受体介导的PANX1激活机制存在不同的结构要求。