Department of Physiology and Biophysics, University of California, Irvine, CA, USA.
Chao Family Comprehensive Cancer Center, University of California, Irvine, CA, USA.
Commun Biol. 2021 Feb 26;4(1):261. doi: 10.1038/s42003-021-01792-0.
Here, we report the identification and characterization of the first proton channels from fungi. The fungal proteins are related to animal voltage-gated Hv channels and are conserved in both higher and lower fungi. Channels from Basidiomycota and Ascomycota appear to be evolutionally and functionally distinct. Representatives from the two phyla share several features with their animal counterparts, including structural organization and strong proton selectivity, but they differ from each other and from animal Hvs in terms of voltage range of activation, pharmacology, and pH sensitivity. The activation gate of Hv channels is believed to be contained within the transmembrane core of the protein and little is known about contributions of peripheral regions to the activation mechanism. Using a chimeragenesis approach, we find that intra- and extracellular peripheral regions are main determinants of the voltage range of activation in fungal channels, highlighting the role of these overlooked components in channel gating.
在这里,我们报告了真菌中第一个质子通道的鉴定和特征。真菌蛋白与动物电压门控 Hv 通道有关,在高等真菌和低等真菌中都保守。担子菌门和子囊菌门的通道似乎在进化和功能上是不同的。来自这两个门的代表与它们的动物对应物有几个共同的特征,包括结构组织和强烈的质子选择性,但它们在激活电压范围、药理学和 pH 敏感性方面彼此不同,也与动物 Hv 不同。Hv 通道的激活门被认为包含在蛋白质的跨膜核心内,对于外周区域对激活机制的贡献知之甚少。使用嵌合方法,我们发现细胞内和细胞外周区域是真菌通道激活电压范围的主要决定因素,突出了这些被忽视的成分在通道门控中的作用。