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

被引:60
|
作者
Schlichthaerle, Thomas [1 ,2 ,3 ]
Strauss, Maximilian T. [1 ,2 ,3 ]
Schueder, Florian [1 ,2 ,3 ]
Auer, Alexander [1 ,2 ,3 ]
Nijmeijer, Bianca [4 ]
Kueblbeck, Moritz [4 ]
Sabinina, Vilma Jimenez [4 ]
Thevathasan, Jervis, V [4 ]
Ries, Jonas [4 ]
Ellenberg, Jan [4 ]
Jungmann, Ralf [1 ,2 ,3 ]
机构
[1] Ludwig Maximilians Univ Munchen, Fac Phys, Geschwister Scholl Pl 1, D-80539 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Ctr Nanosci, Geschwister Scholl Pl 1, D-80539 Munich, Germany
[3] Max Planck Inst Biochem, Klopferspitz 18, D-82152 Martinsried, Germany
[4] EMBL, Cell Biol & Biophys Unit, Meyerhofstr 1, Heidelberg, Germany
基金
美国国家卫生研究院; 欧洲研究理事会;
关键词
DNA-PAINT; genetically encoded tags; nuclear pore complex; single-molecule imaging; super-resolution microscopy; SUPERRESOLUTION MICROSCOPY; MOLECULES; SCAFFOLD; DESIGN;
D O I
10.1002/anie.201905685
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:13004 / 13008
页数:5
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