Evidence map›Paper›PMID 38169470›Full record

ArticleNature communications2024

Dipeptide coacervates as artificial membraneless organelles for bioorthogonal catalysis.

Shoupeng Cao, Tsvetomir Ivanov, Julian Heuer, Calum T J Ferguson, Katharina Landfester, Lucas Caire da Silva

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
22.7field-weighted citation impact, top 1% of its field
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

70 citing papers in PubMed, 132 citations in OpenAlex.

  1. Review
  2. Article
  3. Patchy Membrane-Directed Multiphase Complex Coacervation.Journal of the American Chemical Society · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Reversible Nucleolar Complex Coacervation by Short Cationic Peptides.Journal of the American Chemical Society · 2026
    Article
  11. Article
  12. Let There be Light! Light as an Engine and Regulator in Synthetic Cells.Angewandte Chemie (International ed. in English) · 2026
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Enantiopurity-Dependent Peptide Coacervates and Asymmetric Organocatalysis.Small (Weinheim an der Bergstrasse, Germany) · 2026
    Article
  20. Article

10 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 3 countries.

Shoupeng CaoMax Planck Institute for Polymer Research, 55128, Mainz, Germany.ORCID 0000-0002-5856-2407
Tsvetomir IvanovMax Planck Institute for Polymer Research, 55128, Mainz, Germany.
Julian HeuerMax Planck Institute for Polymer Research, 55128, Mainz, Germany.
Calum T J FergusonMax Planck Institute for Polymer Research, 55128, Mainz, Germany.
Katharina LandfesterMax Planck Institute for Polymer Research, 55128, Mainz, Germany. landfester@mpip-mainz.mpg.de.ORCID 0000-0001-9591-4638
Lucas Caire da SilvaMax Planck Institute for Polymer Research, 55128, Mainz, Germany. silva@mpip-mainz.mpg.de.ORCID 0000-0003-4663-3471
Max Planck Institute for Polymer Research · DE

Funding

Alexander von Humboldt-Stiftung (Alexander von Humboldt Foundation) 3.5-CHN-1222717-HFST-PBundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) MaxSynBioMax-Planck-Gesellschaft (Max Planck Society) MaxSynBio
6 · The paper itself

Abstract

Artificial organelles can manipulate cellular functions and introduce non-biological processes into cells. Coacervate droplets have emerged as a close analog of membraneless cellular organelles. Their biomimetic properties, such as molecular crowding and selective partitioning, make them promising components for designing cell-like materials. However, their use as artificial organelles has been limited by their complex molecular structure, limited control over internal microenvironment properties, and inherent colloidal instability. Here we report the design of dipeptide coacervates that exhibit enhanced stability, biocompatibility, and a hydrophobic microenvironment. The hydrophobic character facilitates the encapsulation of hydrophobic species, including transition metal-based catalysts, enhancing their efficiency in aqueous environments. Dipeptide coacervates carrying a metal-based catalyst are incorporated as active artificial organelles in cells and trigger an internal non-biological chemical reaction. The development of coacervates with a hydrophobic microenvironment opens an alternative avenue in the field of biomimetic materials with applications in catalysis and synthetic biology.

Indexed as

Artificial CellsTransition ElementsBiomolecular CondensatesCatalysisDipeptidesOrganellesDipeptidesTransition Elements

Identifiers

PMID38169470
PMCPMC10761997
OpenAlexW4390509786

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.