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冷冻电镜在 1.9Å 分辨率下解析处于动态脂质环境中的连接蛋白 46/50

Connexin-46/50 in a dynamic lipid environment resolved by CryoEM at 1.9 Å.

机构信息

Department of Chemical Physiology and Biochemistry, Oregon Health and Science University, Portland, OR, 97239, USA.

Department of Chemistry, Portland State University, Portland, OR, 97201, USA.

出版信息

Nat Commun. 2020 Aug 28;11(1):4331. doi: 10.1038/s41467-020-18120-5.

Abstract

Gap junctions establish direct pathways for cells to transfer metabolic and electrical messages. The local lipid environment is known to affect the structure, stability and intercellular channel activity of gap junctions; however, the molecular basis for these effects remains unknown. Here, we incorporate native connexin-46/50 (Cx46/50) intercellular channels into a dual lipid nanodisc system, mimicking a native cell-to-cell junction. Structural characterization by CryoEM reveals a lipid-induced stabilization to the channel, resulting in a 3D reconstruction at 1.9 Å resolution. Together with all-atom molecular dynamics simulations, it is shown that Cx46/50 in turn imparts long-range stabilization to the dynamic local lipid environment that is specific to the extracellular lipid leaflet. In addition, ~400 water molecules are resolved in the CryoEM map, localized throughout the intercellular permeation pathway and contributing to the channel architecture. These results illustrate how the aqueous-lipid environment is integrated with the architectural stability, structure and function of gap junction communication channels.

摘要

间隙连接为细胞之间传递代谢和电信号建立了直接途径。已知局部脂质环境会影响间隙连接的结构、稳定性和细胞间通道活性;然而,这些影响的分子基础仍然未知。在这里,我们将天然连接蛋白-46/50(Cx46/50)细胞间通道纳入双脂质纳米盘系统,模拟天然的细胞-细胞连接。通过低温电子显微镜(CryoEM)进行的结构特征分析显示,通道受到脂质诱导的稳定作用,导致在 1.9Å 分辨率下进行 3D 重建。结合全原子分子动力学模拟,结果表明 Cx46/50 反过来赋予动态局部脂质环境长程稳定性,这种稳定性是特定于细胞外脂质小叶的。此外,在低温电镜图谱中还解析出约 400 个水分子,它们分布在整个细胞间渗透途径中,并有助于通道结构。这些结果说明了水-脂质环境如何与间隙连接通讯通道的结构稳定性、结构和功能相整合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fe6/7455559/c77f98564c39/41467_2020_18120_Fig1_HTML.jpg

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