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原位蛋白质聚集的高级荧光成像。

Advanced fluorescence imaging of in situ protein aggregation.

机构信息

Cambridge Infinitus Research Centre, Department of Chemical Engineering and Biotechnology, University of Cambridge, West Cambridge Site, Philippa Fawcett Drive, Cambridge CB3 0AS, United Kingdom.

出版信息

Phys Biol. 2020 Feb 11;17(2):021001. doi: 10.1088/1478-3975/ab694e.

Abstract

The aggregation of intrinsically disordered proteins is a hallmark of neurodegenerative diseases, such as Alzheimer's, Parkinson's and Huntington's disease. Although we currently have a good molecular level understanding on how protein aggregation occurs in vitro, the details of its self-assembly in live cells are still mainly unknown. During the last ten years, we have witnessed the rapid development of advanced imaging techniques, especially super-resolution and fluorescence lifetime-based microscopy, in different areas of cell biology. These methods have been revolutionising our understanding of how proteins aggregate, providing unprecedented high spatial-temporal resolution which permits us to capture the kinetics of aggregate seeding and expansion, the motion and distribution of individual aggregates within the cells, and its structural change. In this article, we will review the study of in situ protein aggregation using advanced imaging techniques, with the focus on protein aggregate structure and its assembly dynamics.

摘要

无定形蛋白质的聚集是神经退行性疾病(如阿尔茨海默病、帕金森病和亨廷顿病)的一个标志。虽然我们目前对蛋白质在体外聚集的机制有了很好的分子水平理解,但蛋白质在活细胞中的自组装细节仍主要未知。在过去的十年中,我们见证了先进成像技术的快速发展,特别是超分辨率和荧光寿命显微镜技术在细胞生物学的不同领域的应用。这些方法正在彻底改变我们对蛋白质聚集的理解,提供了前所未有的高时空分辨率,使我们能够捕捉到聚集体成核和扩展的动力学、单个聚集体在细胞内的运动和分布,以及其结构变化。在本文中,我们将回顾使用先进成像技术研究原位蛋白质聚集的情况,重点关注蛋白质聚集体的结构及其组装动力学。

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