Nuclear Pore Scaffold Structure Analyzed by Super-Resolution Microscopy and Particle Averaging

被引:325
作者
Szymborska, Anna [1 ]
de Marco, Alex [2 ]
Daigle, Nathalie [1 ]
Cordes, Volker C. [3 ]
Briggs, John A. G. [2 ]
Ellenberg, Jan [1 ]
机构
[1] European Mol Biol Lab, Cell Biol & Biophys Unit, D-69117 Heidelberg, Germany
[2] European Mol Biol Lab, Struct & Computat Biol Unit, D-69117 Heidelberg, Germany
[3] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
关键词
CRYOELECTRON TOMOGRAPHY; FLUORESCENCE MICROSCOPY; COMPLEX; ARCHITECTURE; RESOLUTION; MEMBRANE; NANOSCOPY; PROTEINS; MODULE; COAT;
D O I
10.1126/science.1240672
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Much of life's essential molecular machinery consists of large protein assemblies that currently pose challenges for structure determination. A prominent example is the nuclear pore complex (NPC), for which the organization of its individual components remains unknown. By combining stochastic super-resolution microscopy, to directly resolve the ringlike structure of the NPC, with single particle averaging, to use information from thousands of pores, we determined the average positions of fluorescent molecular labels in the NPC with a precision well below 1 nanometer. Applying this approach systematically to the largest building block of the NPC, the Nup107-160 subcomplex, we assessed the structure of the NPC scaffold. Thus, light microscopy can be used to study the molecular organization of large protein complexes in situ in whole cells.
引用
收藏
页码:655 / 658
页数:4
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