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基于特定选择性过滤器几何结构的钙通道自下而上设计。

Bottom-up design of calcium channels from defined selectivity filter geometry.

作者信息

Liu Yulai, Weidle Connor, Mihaljević Ljubica, Watson Joseph L, Li Zhe, Yu Le Tracy, Majumder Sagardip, Borst Andrew J, Carr Kenneth D, Kibler Ryan D, El-Din Tamer M Gamal, Catterall William A, Baker David

机构信息

Department of Biochemistry, University of Washington, Seattle, WA, USA.

Institute for Protein Design, University of Washington, Seattle, WA, USA.

出版信息

bioRxiv. 2024 Dec 20:2024.12.19.629320. doi: 10.1101/2024.12.19.629320.

DOI:10.1101/2024.12.19.629320
PMID:39763961
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11702685/
Abstract

Native ion channels play key roles in biological systems, and engineered versions are widely used as chemogenetic tools and in sensing devices. Protein design has been harnessed to generate pore-containing transmembrane proteins, but the capability to design ion selectivity based on the interactions between ions and selectivity filter residues, a crucial feature of native ion channels, has been constrained by the lack of methods to place the metal-coordinating residues with atomic-level precision. Here we describe a bottom-up RFdiffusion-based approach to construct Ca channels from defined selectivity filter residue geometries, and use this approach to design symmetric oligomeric channels with Ca selectivity filters having different coordination numbers and different geometries at the entrance of a wide pore buttressed by multiple transmembrane helices. The designed channel proteins assemble into homogenous pore-containing particles, and for both tetrameric and hexameric ion-coordinating configurations, patch-clamp experiments show that the designed channels have higher conductances for Ca than for Na and other divalent ions (Sr and Mg). Cryo-electron microscopy indicates that the design method has high accuracy: the structure of the hexameric Ca channel is nearly identical to the design model. Our bottom-up design approach now enables the testing of hypotheses relating filter geometry to ion selectivity by direct construction, and provides a roadmap for creating selective ion channels for a wide range of applications.

摘要

天然离子通道在生物系统中发挥着关键作用,工程化版本被广泛用作化学遗传工具和传感设备。蛋白质设计已被用于生成含孔的跨膜蛋白,但由于缺乏以原子级精度放置金属配位残基的方法,基于离子与选择性过滤器残基之间的相互作用来设计离子选择性(天然离子通道的一个关键特征)的能力受到了限制。在这里,我们描述了一种基于自下而上的RFdiffusion方法,从确定的选择性过滤器残基几何结构构建钙通道,并使用这种方法设计对称的寡聚通道,其钙选择性过滤器在由多个跨膜螺旋支撑的宽孔入口处具有不同的配位数和不同的几何结构。设计的通道蛋白组装成含有均匀孔的颗粒,对于四聚体和六聚体离子配位构型,膜片钳实验表明,设计的通道对钙的电导率高于对钠和其他二价离子(锶和镁)的电导率。冷冻电子显微镜表明该设计方法具有很高的准确性:六聚体钙通道的结构与设计模型几乎相同。我们的自下而上设计方法现在能够通过直接构建来测试与过滤器几何结构与离子选择性相关的假设,并为创建用于广泛应用的选择性离子通道提供了路线图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/15998869f525/nihpp-2024.12.19.629320v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/574a773a00d7/nihpp-2024.12.19.629320v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/c9ef8b72f21d/nihpp-2024.12.19.629320v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/89f7cac7c5b1/nihpp-2024.12.19.629320v1-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/21ded48e3e02/nihpp-2024.12.19.629320v1-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/6c3e5ba5a371/nihpp-2024.12.19.629320v1-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/b3e990cb7825/nihpp-2024.12.19.629320v1-f0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/704b287f5baf/nihpp-2024.12.19.629320v1-f0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/b631bd693e2a/nihpp-2024.12.19.629320v1-f0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/29894b4627d0/nihpp-2024.12.19.629320v1-f0014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/8342e644607b/nihpp-2024.12.19.629320v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/42be335cc505/nihpp-2024.12.19.629320v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/2661748135c3/nihpp-2024.12.19.629320v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/9c284a5f7181/nihpp-2024.12.19.629320v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/15998869f525/nihpp-2024.12.19.629320v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/574a773a00d7/nihpp-2024.12.19.629320v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/c9ef8b72f21d/nihpp-2024.12.19.629320v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/89f7cac7c5b1/nihpp-2024.12.19.629320v1-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/21ded48e3e02/nihpp-2024.12.19.629320v1-f0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/6c3e5ba5a371/nihpp-2024.12.19.629320v1-f0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/b3e990cb7825/nihpp-2024.12.19.629320v1-f0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/704b287f5baf/nihpp-2024.12.19.629320v1-f0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/b631bd693e2a/nihpp-2024.12.19.629320v1-f0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/29894b4627d0/nihpp-2024.12.19.629320v1-f0014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/8342e644607b/nihpp-2024.12.19.629320v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/42be335cc505/nihpp-2024.12.19.629320v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/2661748135c3/nihpp-2024.12.19.629320v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/9c284a5f7181/nihpp-2024.12.19.629320v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb5/11702685/15998869f525/nihpp-2024.12.19.629320v1-f0005.jpg

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