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使用 DNA-PAINT 技术的遗传编码探针直接可视化单个核孔复合物蛋白

Direct Visualization of Single Nuclear Pore Complex Proteins Using Genetically-Encoded Probes for DNA-PAINT.

机构信息

Faculty of Physics and Center for Nanoscience, LMU Munich, Geschwister-Scholl-Platz 1, 80539, Munich, Germany.

Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.

出版信息

Angew Chem Int Ed Engl. 2019 Sep 9;58(37):13004-13008. doi: 10.1002/anie.201905685. Epub 2019 Aug 21.

Abstract

The nuclear pore complex (NPC) is one of the largest and most complex protein assemblies in the cell and, among other functions, serves as the gatekeeper of nucleocytoplasmic transport. Unraveling its molecular architecture and functioning has been an active research topic for decades with recent cryogenic electron microscopy and super-resolution studies advancing our understanding of the architecture of the NPC complex. However, the specific and direct visualization of single copies of NPC proteins is thus far elusive. Herein, we combine genetically-encoded self-labeling enzymes such as SNAP-tag and HaloTag with DNA-PAINT microscopy. We resolve single copies of nucleoporins in the human Y-complex in three dimensions with a precision of circa 3 nm, enabling studies of multicomponent complexes on the level of single proteins in cells using optical fluorescence microscopy.

摘要

核孔复合体(NPC)是细胞中最大、最复杂的蛋白质组装体之一,具有核质转运的门户等多种功能。几十年来,人们一直致力于研究其分子结构和功能,近年来低温电子显微镜和超分辨率研究提高了我们对 NPC 复合体结构的理解。然而,目前仍难以直接可视化单个 NPC 蛋白。在这里,我们将遗传编码的自标记酶(如 SNAP-tag 和 HaloTag)与 DNA-PAINT 显微镜相结合。我们以大约 3nm 的精度在三维空间中解析了人类 Y 复合物中的单个核孔蛋白,从而可以使用光学荧光显微镜在细胞中单蛋白水平上研究多组分复合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8454/6771475/2cc77ad17258/ANIE-58-13004-g001.jpg

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