具有通用残基标记的三维排列四聚体离子通道的比较结构分析。

IF 3.2 3区 生物学 Q2 BIOPHYSICS Biophysical journal Pub Date : 2025-01-21 Epub Date: 2024-12-17 DOI:10.1016/j.bpj.2024.12.019
Denis B Tikhonov, Vyacheslav S Korkosh, Boris S Zhorov
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引用次数: 0

摘要

尽管四聚体和伪四聚体钾、钠、钙和环核苷酸门控通道具有较大的功能多样性和较差的序列相似性,但它们以及双孔通道、瞬时受体电位通道和异离子型谷氨酸受体在成孔区域具有共同的跨膜(TM)螺旋折叠模式。在每个亚基或重复序列中,孔结构域有两个由再入膜p环连接的TM螺旋。p环包括一个膜下行螺旋P1,它在结构上是这些通道中最保守的元件,以及在离子渗透途径收缩时有助于选择性过滤区域的残基。在24-TM通道中,孔域被4个电压感应域包围,每个域具有4个TM螺旋的保守折叠。通过x射线晶体学或低温电子显微镜已经获得了这些通道的数百个原子尺度结构,称为“p环通道”。蛋白质数据库中p环通道实验结构的数量正在迅速增加。AlphaFold3、RoseTTAFold等计算工具可用于生成缺乏实验结构的P-loop通道的3D模型。虽然p环通道的比较结构分析是可取的,但它受到通道的残差数和三维方向的变化的阻碍。为了解决这个问题,我们开发了一个通用的TM螺旋和p环残基标记方案。我们进一步建立了P-Loop离子通道(PLIC)数据库;www.plic3da.com),目前包含超过400个具有重新标记残基的3d对齐结构。我们使用这个数据库来比较来自不同亚族的通道的多个3D结构。该比较首次采用统计方法,突出了通道折叠中的保守和可变元素,揭示了不规则性,并确定了值得进一步分析的异常值。
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3D-aligned tetrameric ion channels with universal residue labels for comparative structural analysis.

Despite their large functional diversity and poor sequence similarity, tetrameric and pseudotetrameric potassium, sodium, calcium, and cyclic-nucleotide gated channels, as well as two-pore channels, transient receptor potential channels, and ionotropic glutamate receptor channels, share a common folding pattern of the transmembrane (TM) helices in the pore domain. In each subunit or repeat, two TM helices connected by a membrane-reentering P-loop contribute a quarter to the pore domain. The P-loop includes a membrane-descending helix, P1, which is structurally the most conserved element of these channels, and residues that contribute to the selectivity-filter region at the constriction of the ion-permeating pathway. In 24-TM channels, the pore domain is surrounded by four voltage-sensing domains, each with conserved folding of four TM helices. Hundreds of atomic-scale structures of these channels, referred to as "P-loop channels," have been obtained through x-ray crystallography or cryoelectron microscopy. The number of experimental structures of P-loop channels deposited in the PDB is rapidly increasing. AlphaFold3, RoseTTAFold, and other computational tools can be used to generate three-dimensional (3D) models of P-loop channels that lack experimental structures. While comparative structural analysis of P-loop channels is desirable, it is hindered by variations in residue numbers and 3D orientations of the channels. To address this problem, we have developed a universal residue-labeling scheme for TM helices and P-loops. We further created a database of P-loop ion channels, PLIC: www.plic3da.com, which currently includes over 400 3D-aligned structures with relabeled residues. We use this database to compare multiple 3D structures of channels from different subfamilies. The comparison, which for the first time employs statistical methods, highlights conserved and variable elements in the channels' folding, reveals irregularities, and identifies outliers that warrant further analysis.

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来源期刊
Biophysical journal
Biophysical journal 生物-生物物理
CiteScore
6.10
自引率
5.90%
发文量
3090
审稿时长
2 months
期刊介绍: BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.
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