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一种 K 通道在原子分辨率下的门控循环。

The gating cycle of a K channel at atomic resolution.

机构信息

Center for Membrane Protein Research, Department of Cell Physiology and Molecular Biophysics, Texas Tech University Health Sciences Center, Lubbock, United States.

Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, United States.

出版信息

Elife. 2017 Nov 22;6:e28032. doi: 10.7554/eLife.28032.

DOI:10.7554/eLife.28032
PMID:29165243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5711375/
Abstract

C-type inactivation in potassium channels helps fine-tune long-term channel activity through conformational changes at the selectivity filter. Here, through the use of cross-linked constitutively open constructs, we determined the structures of KcsA's mutants that stabilize the selectivity filter in its conductive (E71A, at 2.25 Å) and deep C-type inactivated (Y82A at 2.4 Å) conformations. These structural snapshots represent KcsA's transient open-conductive (O/O) and the stable open deep C-type inactivated states (O/I), respectively. The present structures provide an unprecedented view of the selectivity filter backbone in its collapsed deep C-type inactivated conformation, highlighting the close interactions with structural waters and the local allosteric interactions that couple activation and inactivation gating. Together with the structures associated with the closed-inactivated state (C/I) and in the well-known closed conductive state (C/O), this work recapitulates, at atomic resolution, the key conformational changes of a potassium channel pore domain as it progresses along its gating cycle.

摘要

钾通道中的 C 型失活通过选择性滤器的构象变化帮助微调长期的通道活性。在这里,我们通过使用交联的组成性开放构建体,确定了稳定选择性滤器处于导电(E71A,在 2.25Å)和深 C 型失活(Y82A,在 2.4Å)构象的 KcsA 突变体的结构。这些结构快照分别代表 KcsA 的瞬时开放导电(O/O)和稳定的开放深 C 型失活状态(O/I)。目前的结构提供了一个前所未有的选择性滤器骨架在其坍塌的深 C 型失活构象中的视图,突出了与结构水的紧密相互作用以及激活和失活门控的局部变构相互作用。与与关闭失活状态(C/I)和众所周知的关闭导电状态(C/O)相关的结构一起,这项工作以原子分辨率重现了钾通道孔域沿着其门控循环的关键构象变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/cf44e73f9d79/elife-28032-fig8-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/b3c2aa992765/elife-28032-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/6ce91c785ea8/elife-28032-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/9aa804438683/elife-28032-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/bc4796f1caf6/elife-28032-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/12d9e019cc78/elife-28032-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/b5c1910ea1d2/elife-28032-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/c95b353bb00e/elife-28032-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/a98a55ae95c3/elife-28032-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/9857fdc117f6/elife-28032-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/cf44e73f9d79/elife-28032-fig8-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/b3c2aa992765/elife-28032-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/6ce91c785ea8/elife-28032-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/9aa804438683/elife-28032-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/bc4796f1caf6/elife-28032-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/12d9e019cc78/elife-28032-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/b5c1910ea1d2/elife-28032-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/c95b353bb00e/elife-28032-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/a98a55ae95c3/elife-28032-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/9857fdc117f6/elife-28032-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e3e/5711375/cf44e73f9d79/elife-28032-fig8-figsupp1.jpg

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