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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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 |
work_keys_str_mv |
AT giuliapaci moleculardeterminantsoflargecargotransportintothenucleus AT tiantianzheng moleculardeterminantsoflargecargotransportintothenucleus AT joanacaria moleculardeterminantsoflargecargotransportintothenucleus AT antonzilman moleculardeterminantsoflargecargotransportintothenucleus AT edwardalemke moleculardeterminantsoflargecargotransportintothenucleus |
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1721458286681653248 |