Evidence map›Paper›PMID 31988132›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Organelle-specific targeting of polymersomes into the cell nucleus.

Christina Zelmer, Ludovit P Zweifel, Larisa E Kapinos, Ioana Craciun, Zekiye P Güven, Cornelia G Palivan, Roderick Y H Lim

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

34 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Designing the Next Generation of Biomaterials through Nanoengineering.Advanced materials (Deerfield Beach, Fla.) · 2025
    Review
  7. Review
  8. Nanocarriers for cutting-edge cancer immunotherapies.Journal of translational medicine · 2025
    Review
  9. Article
  10. Organelle-Targeting Nanoparticles.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  11. Review
  12. Article
  13. Review
  14. Nanoparticle-Based Immunotherapy for Reversing T-Cell Exhaustion.International journal of molecular sciences · 2024
    Review
  15. Article
  16. Review
  17. Nanomedicine in cancer therapy.Signal transduction and targeted therapy · 2023
    Review
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Christina ZelmerBiozentrum and the Swiss Nanoscience Institute, University of Basel, CH-4056 Basel, Switzerland.
Ludovit P ZweifelBiozentrum and the Swiss Nanoscience Institute, University of Basel, CH-4056 Basel, Switzerland.
Larisa E KapinosBiozentrum and the Swiss Nanoscience Institute, University of Basel, CH-4056 Basel, Switzerland.
Ioana CraciunDepartment of Chemistry, University of Basel, CH-4002 Basel, Switzerland.
Zekiye P GüvenInstitute of Materials, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland.
Cornelia G PalivanDepartment of Chemistry, University of Basel, CH-4002 Basel, Switzerland; cornelia.palivan@unibas.ch roderick.lim@unibas.ch.ORCID 0000-0001-7777-5355
Roderick Y H LimBiozentrum and the Swiss Nanoscience Institute, University of Basel, CH-4056 Basel, Switzerland; cornelia.palivan@unibas.ch roderick.lim@unibas.ch.ORCID 0000-0001-5015-6087

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organelle-specific nanocarriers (NCs) are highly sought after for delivering therapeutic agents into the cell nucleus. This necessitates nucleocytoplasmic transport (NCT) to bypass nuclear pore complexes (NPCs). However, little is known as to how comparably large NCs infiltrate this vital intracellular barrier to enter the nuclear interior. Here, we developed nuclear localization signal (NLS)-conjugated polymersome nanocarriers (NLS-NCs) and studied the NCT mechanism underlying their selective nuclear uptake. Detailed chemical, biophysical, and cellular analyses show that karyopherin receptors are required to authenticate, bind, and escort NLS-NCs through NPCs while Ran guanosine triphosphate (RanGTP) promotes their release from NPCs into the nuclear interior. Ultrastructural analysis by regressive staining transmission electron microscopy further resolves the NLS-NCs on transit in NPCs and inside the nucleus. By elucidating their ability to utilize NCT, these findings demonstrate the efficacy of polymersomes to deliver encapsulated payloads directly into cell nuclei.

Indexed as

Active Transport, Cell NucleusBiocompatible MaterialsCell NucleusDrug Delivery SystemsGuanosine TriphosphateHeLa CellsHumansKaryopherinsNanoparticlesNuclear Localization SignalsNuclear PorePolymersBiocompatible MaterialsGuanosine TriphosphateKaryopherinsNuclear Localization SignalsPolymersdrug deliverynanocarriernuclear pore complexnucleocytoplasmic transportpolymersome

Identifiers

PMID31988132
PMCPMC7022206

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.