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Programmed Self-Assembly of a Biochemical and Magnetic Scaffold to Trigger and Manipulate Microtubule Structures

机译:生化和电磁支架的程序化自组装以触发和操纵微管结构。

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摘要

Artificial bio-based scaffolds offer broad applications in bioinspired chemistry, nanomedicine, and material science. One current challenge is to understand how the programmed self-assembly of biomolecules at the nanometre level can dictate the emergence of new functional properties at the mesoscopic scale. Here we report a general approach to design genetically encoded protein-based scaffolds with modular biochemical and magnetic functions. By combining chemically induced dimerization strategies and biomineralisation, we engineered ferritin nanocages to nucleate and manipulate microtubule structures upon magnetic actuation. Triggering the self-assembly of engineered ferritins into micrometric scaffolds mimics the function of centrosomes, the microtubule organizing centres of cells, and provides unique magnetic and self-organizing properties. We anticipate that our approach could be transposed to control various biological processes and extend to broader applications in biotechnology or material chemistry.
机译:人造生物基支架在生物启发化学,纳米医学和材料科学中提供了广泛的应用。当前的挑战是要了解在纳米水平上编程的生物分子自组装如何指示介观尺度上新功能特性的出现。在这里,我们报告一种通用的方法来设计具有模块化生化和磁性功能的遗传编码的基于蛋白质的支架。通过结合化学诱导的二聚化策略和生物矿化,我们设计了铁蛋白纳米笼,以在磁驱动时成核并操纵微管结构。触发将工程铁蛋白自组装为微米级支架,可模仿中心体(细胞的微管组织中心)的功能,并提供独特的磁性和自组织特性。我们期望我们的方法可以转变为控制各种生物过程,并扩展到生物技术或材料化学中的广泛应用。

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