Molecular determinants of large cargo transport into the nucleus

Nucleocytoplasmic transport is tightly regulated by the nuclear pore complex (NPC). Among the thousands of molecules that cross the NPC, even very large (>15 nm) cargoes such as pathogens, mRNAs and pre-ribosomes can pass the NPC intact. For these cargoes, there is little quantitative underst...

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Main Authors: Giulia Paci, Tiantian Zheng, Joana Caria, Anton Zilman, Edward A Lemke
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-07-01
Series:eLife
Subjects:
NLS
Online Access:https://elifesciences.org/articles/55963
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spelling doaj-b30c20a161e7437592db31f594ab1c202021-05-05T21:19:43ZengeLife Sciences Publications LtdeLife2050-084X2020-07-01910.7554/eLife.55963Molecular determinants of large cargo transport into the nucleusGiulia Paci0https://orcid.org/0000-0003-0565-4356Tiantian Zheng1Joana Caria2Anton Zilman3https://orcid.org/0000-0002-8523-6703Edward A Lemke4https://orcid.org/0000-0002-0634-0503Biocentre, Johannes Gutenberg-University Mainz, Mainz, Germany; Institute of Molecular Biology, Mainz, Germany; European Molecular Biology Laboratory, Heidelberg, GermanyDepartment of Physics, University of Toronto, Toronto, CanadaBiocentre, Johannes Gutenberg-University Mainz, Mainz, Germany; Institute of Molecular Biology, Mainz, Germany; European Molecular Biology Laboratory, Heidelberg, GermanyDepartment of Physics, University of Toronto, Toronto, Canada; Institute for Biomaterials and Biomedical Engineering (IBBME), University of Toronto, Toronto, CanadaBiocentre, Johannes Gutenberg-University Mainz, Mainz, Germany; Institute of Molecular Biology, Mainz, Germany; European Molecular Biology Laboratory, Heidelberg, GermanyNucleocytoplasmic transport is tightly regulated by the nuclear pore complex (NPC). Among the thousands of molecules that cross the NPC, even very large (>15 nm) cargoes such as pathogens, mRNAs and pre-ribosomes can pass the NPC intact. For these cargoes, there is little quantitative understanding of the requirements for their nuclear import, especially the role of multivalent binding to transport receptors via nuclear localisation sequences (NLSs) and the effect of size on import efficiency. Here, we assayed nuclear import kinetics of 30 large cargo models based on four capsid-like particles in the size range of 17–36 nm, with tuneable numbers of up to 240 NLSs. We show that the requirements for nuclear transport can be recapitulated by a simple two-parameter biophysical model that correlates the import flux with the energetics of large cargo transport through the NPC. Together, our results reveal key molecular determinants of large cargo import in cells.https://elifesciences.org/articles/55963nuclear transportpermeabilized cellslarge cargoimport kineticsNLScapsid
collection DOAJ
language English
format Article
sources DOAJ
author Giulia Paci
Tiantian Zheng
Joana Caria
Anton Zilman
Edward A Lemke
spellingShingle Giulia Paci
Tiantian Zheng
Joana Caria
Anton Zilman
Edward A Lemke
Molecular determinants of large cargo transport into the nucleus
eLife
nuclear transport
permeabilized cells
large cargo
import kinetics
NLS
capsid
author_facet Giulia Paci
Tiantian Zheng
Joana Caria
Anton Zilman
Edward A Lemke
author_sort Giulia Paci
title Molecular determinants of large cargo transport into the nucleus
title_short Molecular determinants of large cargo transport into the nucleus
title_full Molecular determinants of large cargo transport into the nucleus
title_fullStr Molecular determinants of large cargo transport into the nucleus
title_full_unstemmed Molecular determinants of large cargo transport into the nucleus
title_sort molecular determinants of large cargo transport into the nucleus
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2020-07-01
description Nucleocytoplasmic transport is tightly regulated by the nuclear pore complex (NPC). Among the thousands of molecules that cross the NPC, even very large (>15 nm) cargoes such as pathogens, mRNAs and pre-ribosomes can pass the NPC intact. For these cargoes, there is little quantitative understanding of the requirements for their nuclear import, especially the role of multivalent binding to transport receptors via nuclear localisation sequences (NLSs) and the effect of size on import efficiency. Here, we assayed nuclear import kinetics of 30 large cargo models based on four capsid-like particles in the size range of 17–36 nm, with tuneable numbers of up to 240 NLSs. We show that the requirements for nuclear transport can be recapitulated by a simple two-parameter biophysical model that correlates the import flux with the energetics of large cargo transport through the NPC. Together, our results reveal key molecular determinants of large cargo import in cells.
topic nuclear transport
permeabilized cells
large cargo
import kinetics
NLS
capsid
url https://elifesciences.org/articles/55963
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AT tiantianzheng moleculardeterminantsoflargecargotransportintothenucleus
AT joanacaria moleculardeterminantsoflargecargotransportintothenucleus
AT antonzilman moleculardeterminantsoflargecargotransportintothenucleus
AT edwardalemke moleculardeterminantsoflargecargotransportintothenucleus
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