Super-resolution 3D tomography of interactions and competition in the nuclear pore complex

被引:49
作者
Ma, Jiong [1 ,2 ]
Goryaynov, Alexander [1 ,3 ]
Yang, Weidong [1 ]
机构
[1] Temple Univ, Dept Biol, Philadelphia, PA 19122 USA
[2] Fudan Univ, Dept Opt Sci & Engn, Shanghai 200433, Peoples R China
[3] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
基金
美国国家卫生研究院;
关键词
IMPORTIN-BETA; NUCLEOCYTOPLASMIC TRANSPORT; SINGLE-MOLECULE; NUCLEOPORINS; TRANSLOCATION; EXPORT; MECHANISM; HYDROGEL; BARRIER; BINDING;
D O I
10.1038/nsmb.3174
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A selective barrier formed by intrinsically disordered Phe-Gly (FG) nucleoporins (Nups) allows transport receptor (TR)-facilitated translocation of signal-dependent cargos through the nuclear pore complexes (NPCs) of eukaryotic cells. However, the configuration of the FG-Nup barrier and its interactions with multiple TRs in native NPCs remain obscure. Here, we mapped the interaction sites of various TRs or FG segments within the FG-Nup barrier by using high-speed super-resolution microscopy and used these sites to reconstruct the three-dimensional tomography of the native barrier in the NPC. We found that each TR possesses a unique interaction zone within the FG-Nup barrier and that two major TRs, importin beta 1 and Crm1, outcompete other TRs in binding FG Nups. Moreover, TRs may alter the tomography of the FG-Nup barrier and affect one another's pathways under circumstances of heavy competition.
引用
收藏
页码:239 / 247
页数:9
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