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DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex

The nuclear pore complex (NPC) is the gatekeeper for nuclear transport in eukaryotic cells. A key component of the NPC is the central shaft lined with intrinsically disordered proteins (IDPs) known as FG-Nups, which control the selective molecular traffic. Here, we present an approach to realize art...

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Autores principales: Ketterer, Philip, Ananth, Adithya N., Laman Trip, Diederik S., Mishra, Ankur, Bertosin, Eva, Ganji, Mahipal, van der Torre, Jaco, Onck, Patrick, Dietz, Hendrik, Dekker, Cees
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834454/
https://www.ncbi.nlm.nih.gov/pubmed/29500415
http://dx.doi.org/10.1038/s41467-018-03313-w
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author Ketterer, Philip
Ananth, Adithya N.
Laman Trip, Diederik S.
Mishra, Ankur
Bertosin, Eva
Ganji, Mahipal
van der Torre, Jaco
Onck, Patrick
Dietz, Hendrik
Dekker, Cees
author_facet Ketterer, Philip
Ananth, Adithya N.
Laman Trip, Diederik S.
Mishra, Ankur
Bertosin, Eva
Ganji, Mahipal
van der Torre, Jaco
Onck, Patrick
Dietz, Hendrik
Dekker, Cees
author_sort Ketterer, Philip
collection PubMed
description The nuclear pore complex (NPC) is the gatekeeper for nuclear transport in eukaryotic cells. A key component of the NPC is the central shaft lined with intrinsically disordered proteins (IDPs) known as FG-Nups, which control the selective molecular traffic. Here, we present an approach to realize artificial NPC mimics that allows controlling the type and copy number of FG-Nups. We constructed 34 nm-wide 3D DNA origami rings and attached different numbers of NSP1, a model yeast FG-Nup, or NSP1-S, a hydrophilic mutant. Using (cryo) electron microscopy, we find that NSP1 forms denser cohesive networks inside the ring compared to NSP1-S. Consistent with this, the measured ionic conductance is lower for NSP1 than for NSP1-S. Molecular dynamics simulations reveal spatially varying protein densities and conductances in good agreement with the experiments. Our technique provides an experimental platform for deciphering the collective behavior of IDPs with full control of their type and position.
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spelling pubmed-58344542018-03-06 DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex Ketterer, Philip Ananth, Adithya N. Laman Trip, Diederik S. Mishra, Ankur Bertosin, Eva Ganji, Mahipal van der Torre, Jaco Onck, Patrick Dietz, Hendrik Dekker, Cees Nat Commun Article The nuclear pore complex (NPC) is the gatekeeper for nuclear transport in eukaryotic cells. A key component of the NPC is the central shaft lined with intrinsically disordered proteins (IDPs) known as FG-Nups, which control the selective molecular traffic. Here, we present an approach to realize artificial NPC mimics that allows controlling the type and copy number of FG-Nups. We constructed 34 nm-wide 3D DNA origami rings and attached different numbers of NSP1, a model yeast FG-Nup, or NSP1-S, a hydrophilic mutant. Using (cryo) electron microscopy, we find that NSP1 forms denser cohesive networks inside the ring compared to NSP1-S. Consistent with this, the measured ionic conductance is lower for NSP1 than for NSP1-S. Molecular dynamics simulations reveal spatially varying protein densities and conductances in good agreement with the experiments. Our technique provides an experimental platform for deciphering the collective behavior of IDPs with full control of their type and position. Nature Publishing Group UK 2018-03-02 /pmc/articles/PMC5834454/ /pubmed/29500415 http://dx.doi.org/10.1038/s41467-018-03313-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ketterer, Philip
Ananth, Adithya N.
Laman Trip, Diederik S.
Mishra, Ankur
Bertosin, Eva
Ganji, Mahipal
van der Torre, Jaco
Onck, Patrick
Dietz, Hendrik
Dekker, Cees
DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex
title DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex
title_full DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex
title_fullStr DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex
title_full_unstemmed DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex
title_short DNA origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex
title_sort dna origami scaffold for studying intrinsically disordered proteins of the nuclear pore complex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834454/
https://www.ncbi.nlm.nih.gov/pubmed/29500415
http://dx.doi.org/10.1038/s41467-018-03313-w
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