核孔
显微镜
分辨率(逻辑)
支架蛋白
粒子(生态学)
荧光显微镜
高分辨率
超分辨显微术
生物物理学
纳米技术
生物系统
材料科学
荧光
化学
计算机科学
物理
光学
生物
人工智能
扫描共焦电子显微镜
核心
细胞生物学
生物化学
生态学
信号转导
遥感
地质学
作者
Anna Szymborska,Alex de Marco,Nathalie Daigle,Volker C. Cordes,John A. G. Briggs,Jan Ellenberg
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-07-12
卷期号:341 (6146): 655-658
被引量:478
标识
DOI:10.1126/science.1240672
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI