Nanoscale Visualization of Drosophila E-cadherin Ectodomain Fragments and Their Interactions Using DNA Origami Nanoblocks.

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hiroki Oda, Shigetaka Nishiguchi, Chihong Song, Kazuyoshi Murata, Takayuki Uchihashi, Yuki Suzuki
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引用次数: 0

Abstract

The adhesive function of cell surface proteins can be visually assessed through direct observation; however, the underlying structures that mediate adhesion typically remain invisible at the nanoscale level. This hinders knowledge on the diversity of molecular architectures responsible for cell-cell adhesion. Drosophila E-cadherin (DE-cadherin), a classical cadherin with a unique domain structure, demonstrates adhesive function; however, it lacks a structural model that explains its adhesion mechanism. Here, we present a novel application of DNA origami technology to create a cell-free, flat environment in which full DE-cadherin ectodomains are anchored using SNAP-tags and biotin-streptavidin interactions. DNA origami was assembled into a 120 nm long block, bearing 5 or 14 biotin:streptavidin sites that were evenly spaced on one lateral face. DE-cadherin ectodomain fragments were attached via biotinylated SNAP-tags. These decorated DNA origami nanoblocks were subjected to transmission electron and high-speed atomic force microscopy, which revealed a hinge-like site that separated the membrane-distal and -proximal portions of the DE-cadherin ectodomain, suggesting a role in mechanical flexibility. We also observed interactions between DE-cadherin ectodomains via their membrane-distal portions on single DNA origami nanoblocks. We reconstituted an adhesion-like process via pairing DNA origami nanoblocks using DE-cadherin ectodomain interactions. Homophilic associations of functional DE-cadherin ectodomains between the paired DNA origami nanoblocks were visualized at the nanoscale, displaying strand-like molecular configurations, likely representing the extracellular cadherin repeats without regular arrays of structural elements. This study introduces a DNA origami-based platform for reconstituting and visualizing cadherin ectodomain interactions, with potential applications for a broader range of adhesion molecules.

利用 DNA 折纸纳米块对果蝇 E-cadherin 外结构域片段及其相互作用进行纳米级可视化。
细胞表面蛋白的粘附功能可通过直接观察进行直观评估;然而,介导粘附的底层结构在纳米尺度水平上通常是不可见的。这阻碍了人们对细胞间粘附的分子结构多样性的了解。果蝇 E-粘附蛋白(DE-cadherin)是一种具有独特结构域的经典粘附蛋白,具有粘附功能;然而,它缺乏一种结构模型来解释其粘附机制。在这里,我们展示了一种新颖的 DNA 折纸技术应用,利用 SNAP 标签和生物素-链霉亲和素的相互作用创造了一个无细胞的平面环境,在这个环境中,DE-cadherin 的外结构域被完整地锚定。DNA 折纸被组装成 120 nm 长的块状,在一个侧面上均匀分布着 5 或 14 个生物素-链霉亲和素位点。通过生物素化的 SNAP 标签连接 DE-cadherin 外结构域片段。对这些装饰过的 DNA 折纸纳米块进行了透射电子显微镜和高速原子力显微镜观察,结果显示,DE-cadherin 外结构域的膜远端和膜近端之间有一个类似铰链的部位,这表明它在机械灵活性方面发挥了作用。我们还在单个DNA折纸纳米块上观察到了DE-cadherin外结构域之间通过膜远端部分的相互作用。我们利用DE-cadherin外结构域之间的相互作用,通过配对DNA折纸纳米块重建了一个类似粘附的过程。配对的DNA折纸纳米块之间的功能性DE-cadherin外结构域的同亲结合在纳米尺度上被可视化,显示出类似于链状的分子构型,很可能代表了细胞外cadherin重复序列,而没有规则的结构元素阵列。这项研究介绍了一种基于DNA折纸的平台,用于重构和可视化粘连蛋白外结构域的相互作用,有望应用于更广泛的粘连分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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