Cargando…
Assembly of Nsp1 Nucleoporins Provides Insight into Nuclear Pore Complex Gating
Nuclear pore complexes (NPCs) form gateways for material transfer across the nuclear envelope of eukaryotic cells. Disordered proteins, rich in phenylalanine-glycine repeat motifs (FG-nups), form the central transport channel. Understanding how nups are arranged in the interior of the NPC may explai...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952814/ https://www.ncbi.nlm.nih.gov/pubmed/24626154 http://dx.doi.org/10.1371/journal.pcbi.1003488 |
_version_ | 1782307262770970624 |
---|---|
author | Gamini, Ramya Han, Wei Stone, John E. Schulten, Klaus |
author_facet | Gamini, Ramya Han, Wei Stone, John E. Schulten, Klaus |
author_sort | Gamini, Ramya |
collection | PubMed |
description | Nuclear pore complexes (NPCs) form gateways for material transfer across the nuclear envelope of eukaryotic cells. Disordered proteins, rich in phenylalanine-glycine repeat motifs (FG-nups), form the central transport channel. Understanding how nups are arranged in the interior of the NPC may explain how NPC functions as a selectivity filter for transport of large molecules and a sieve-like filter for diffusion of small molecules (<[Image: see text] or [Image: see text]). We employed molecular dynamics to model the structures formed by various assemblies of one kind of nup, namely the 609-aa-long FG domain of Nsp1 (Nsp1-FG). The simulations started from different initial conformations and geometrical arrangements of Nsp1-FGs. In all cases Nsp1-FGs collectively formed brush-like structures with bristles made of bundles of 2–27 nups, however, the bundles being cross-linked through single nups leaving one bundle and joining a nearby one. The degree of cross-linking varies with different initial nup conformations and arrangements. Structural analysis reveals that FG-repeats of the nups not only involve formation of bundle structures, but are abundantly present in cross-linking regions where the epitopes of FG-repeats are highly accessible. Large molecules that are assisted by transport factors (TFs) are selectively transported through NPC apparently by binding to FG-nups through populated FG-binding pockets on the TF surface. Therefore, our finding suggests that TFs bind concertedly to multiple FGs in cross-linking regions and break-up the bundles to create wide pores for themselves and their cargoes to pass. In addition, the cross-linking between Nsp1-FG bundles, arising from simulations, is found to set a molecular size limit of <[Image: see text] [Image: see text] for passive diffusion of molecules. Our simulations suggest that the NPC central channel, near the periphery where tethering of nups is dominant, features brush-like moderately cross-linked bundles, but in the central region, where tethering loses its effect, features a sieve-like structure of bundles and frequent cross-links. |
format | Online Article Text |
id | pubmed-3952814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39528142014-03-18 Assembly of Nsp1 Nucleoporins Provides Insight into Nuclear Pore Complex Gating Gamini, Ramya Han, Wei Stone, John E. Schulten, Klaus PLoS Comput Biol Research Article Nuclear pore complexes (NPCs) form gateways for material transfer across the nuclear envelope of eukaryotic cells. Disordered proteins, rich in phenylalanine-glycine repeat motifs (FG-nups), form the central transport channel. Understanding how nups are arranged in the interior of the NPC may explain how NPC functions as a selectivity filter for transport of large molecules and a sieve-like filter for diffusion of small molecules (<[Image: see text] or [Image: see text]). We employed molecular dynamics to model the structures formed by various assemblies of one kind of nup, namely the 609-aa-long FG domain of Nsp1 (Nsp1-FG). The simulations started from different initial conformations and geometrical arrangements of Nsp1-FGs. In all cases Nsp1-FGs collectively formed brush-like structures with bristles made of bundles of 2–27 nups, however, the bundles being cross-linked through single nups leaving one bundle and joining a nearby one. The degree of cross-linking varies with different initial nup conformations and arrangements. Structural analysis reveals that FG-repeats of the nups not only involve formation of bundle structures, but are abundantly present in cross-linking regions where the epitopes of FG-repeats are highly accessible. Large molecules that are assisted by transport factors (TFs) are selectively transported through NPC apparently by binding to FG-nups through populated FG-binding pockets on the TF surface. Therefore, our finding suggests that TFs bind concertedly to multiple FGs in cross-linking regions and break-up the bundles to create wide pores for themselves and their cargoes to pass. In addition, the cross-linking between Nsp1-FG bundles, arising from simulations, is found to set a molecular size limit of <[Image: see text] [Image: see text] for passive diffusion of molecules. Our simulations suggest that the NPC central channel, near the periphery where tethering of nups is dominant, features brush-like moderately cross-linked bundles, but in the central region, where tethering loses its effect, features a sieve-like structure of bundles and frequent cross-links. Public Library of Science 2014-03-13 /pmc/articles/PMC3952814/ /pubmed/24626154 http://dx.doi.org/10.1371/journal.pcbi.1003488 Text en © 2014 Gamini et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Gamini, Ramya Han, Wei Stone, John E. Schulten, Klaus Assembly of Nsp1 Nucleoporins Provides Insight into Nuclear Pore Complex Gating |
title | Assembly of Nsp1 Nucleoporins Provides Insight into Nuclear Pore Complex Gating |
title_full | Assembly of Nsp1 Nucleoporins Provides Insight into Nuclear Pore Complex Gating |
title_fullStr | Assembly of Nsp1 Nucleoporins Provides Insight into Nuclear Pore Complex Gating |
title_full_unstemmed | Assembly of Nsp1 Nucleoporins Provides Insight into Nuclear Pore Complex Gating |
title_short | Assembly of Nsp1 Nucleoporins Provides Insight into Nuclear Pore Complex Gating |
title_sort | assembly of nsp1 nucleoporins provides insight into nuclear pore complex gating |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952814/ https://www.ncbi.nlm.nih.gov/pubmed/24626154 http://dx.doi.org/10.1371/journal.pcbi.1003488 |
work_keys_str_mv | AT gaminiramya assemblyofnsp1nucleoporinsprovidesinsightintonuclearporecomplexgating AT hanwei assemblyofnsp1nucleoporinsprovidesinsightintonuclearporecomplexgating AT stonejohne assemblyofnsp1nucleoporinsprovidesinsightintonuclearporecomplexgating AT schultenklaus assemblyofnsp1nucleoporinsprovidesinsightintonuclearporecomplexgating |