Barrier properties of Nup98 FG phases ruled by FG motif identity and inter-FG spacer length.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
10 02 2023
Historique:
received: 14 10 2022
accepted: 24 01 2023
pubmed: 11 2 2023
medline: 15 2 2023
entrez: 10 2 2023
Statut: epublish

Résumé

Nup98 FG repeat domains comprise hydrophobic FG motifs linked through uncharged spacers. FG motifs capture nuclear transport receptors (NTRs) during nuclear pore complex (NPC) passage, confer inter-repeat cohesion, and condense the domains into a selective phase with NPC-typical barrier properties. We show that shortening inter-FG spacers enhances cohesion, increases phase density, and tightens such barrier - all consistent with a sieve-like phase. Phase separation tolerates mutating the Nup98-typical GLFG motifs, provided domain-hydrophobicity remains preserved. NTR-entry, however, is sensitive to (certain) deviations from canonical FG motifs, suggesting co-evolutionary adaptation. Unexpectedly, we observed that arginines promote FG-phase-entry apparently also by hydrophobic interactions/ hydrogen-bonding and not just through cation-π interactions. Although incompatible with NTR·cargo complexes, a YG phase displays remarkable transport selectivity, particularly for engineered GFP

Identifiants

pubmed: 36765044
doi: 10.1038/s41467-023-36331-4
pii: 10.1038/s41467-023-36331-4
pmc: PMC9918544
doi:

Substances chimiques

Nuclear Pore Complex Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

747

Informations de copyright

© 2023. The Author(s).

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Auteurs

Sheung Chun Ng (SC)

Department of Cellular Logistics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.

Abin Biswas (A)

Quantitative Biology, IRI Life Sciences, Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Biological Optomechanics, Max Planck Institute for the Science of Light, Erlangen, Germany.

Trevor Huyton (T)

Department of Cellular Logistics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.

Jürgen Schünemann (J)

Department of Cellular Logistics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.

Simone Reber (S)

Quantitative Biology, IRI Life Sciences, Humboldt-Universität zu Berlin, Berlin, Germany.

Dirk Görlich (D)

Department of Cellular Logistics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany. goerlich@mpinat.mpg.de.

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Classifications MeSH