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Assembly and Mechanical Properties of the Cargo-Free and Cargo Loaded Bacterial Nanocompartment Encapsulin

机译:无货物和载货细菌纳米隔室胶囊蛋白的组装和力学性能

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摘要

Prokaryotes mostly lack membranous compartments that are typical of eukaryotic cells, but instead, they have various protein-based organelles. These include bacterial microcompartments like the carboxysome and the virus-like nanocompartment encapsulin. Encapsulins have an adaptable mechanism for enzyme packaging, which makes it an attractive platform to carry a foreign protein cargo. Here we investigate the assembly pathways and mechanical properties of the cargo-free and cargo-loaded nanocompartments, using a combination of native mass spectrometry, atomic force microscopy and multiscale computational molecular modeling. We show that encapsulin dimers assemble into rigid single-enzyme bacterial containers. Moreover, we demonstrate that cargo encapsulation has a mechanical impact on the shell. The structural similarity of encapsulins to virus capsids is reflected in their mechanical properties. With these robust mechanical properties encapsulins provide a suitable platform for the development of nanotechnological applications.
机译:原核生物大多缺乏真核细胞典型的膜区室,但它们却具有多种基于蛋白质的细胞器。这些包括细菌微隔室,例如羧基体和病毒样纳米隔室胶囊蛋白。胶囊蛋白具有酶包装的适应性机制,这使其成为携带外来蛋白质货物的有吸引力的平台。在这里,我们结合自然质谱,原子力显微镜和多尺度计算分子模型,研究了无货物和载有货物的纳米隔室的组装途径和机械性能。我们表明,胶囊蛋白二聚体组装成刚性的单酶细菌容器。此外,我们证明了货物封装对壳体具有机械影响。胶囊蛋白与病毒衣壳的结构相似性反映在它们的机械性能上。凭借这些强大的机械性能,胶囊蛋白为纳米技术应用的开发提供了合适的平台。

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