Smith Ewan St J, Zhang Xuming, Cadiou Hervé, McNaughton Peter A
Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1PD, United Kingdom.
Neurosci Lett. 2007 Oct 9;426(1):12-7. doi: 10.1016/j.neulet.2007.07.047. Epub 2007 Aug 8.
Most acid-sensing ion channel (ASIC) subunits are activated by protons, but ASIC2b (a splice variant of ASIC2a) is acid-insensitive. Differences in protonatable residues between the extracellular loop regions of ASIC2a and ASIC2b may explain this difference. Site-directed mutagenesis, combined with immunocytochemistry and whole-cell patch clamp, demonstrated that mutating any one of five ASIC2a sites produces channels that traffic normally to the cell surface membrane but are insensitive to protons. One of the mutants forms functional heteromers with ASIC1a and ASIC2a, demonstrating that ion transport is intact in this mutant. These five sites may be involved in the activation of ASIC2a by protons.
大多数酸敏感离子通道(ASIC)亚基可被质子激活,但ASIC2b(ASIC2a的一种剪接变体)对酸不敏感。ASIC2a和ASIC2b细胞外环区域之间可质子化残基的差异可能解释了这种差异。定点诱变结合免疫细胞化学和全细胞膜片钳技术表明,突变ASIC2a的五个位点中的任何一个都会产生能正常转运到细胞表面膜但对质子不敏感的通道。其中一个突变体与ASIC1a和ASIC2a形成功能性异聚体,表明该突变体中的离子转运功能完好。这五个位点可能参与了ASIC2a被质子激活的过程。