Evidence map›Paper›PMID 34815410›Full record

ArticleNature communications2021

Reversible and spatiotemporal control of colloidal structure formation.

H Dehne, A Reitenbach, A R Bausch

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. A DNA-encoded recipe to direct multistage colloidal assembly.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
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

3 authors.

H DehneCenter for Protein Assemblies (CPA) and Lehrstuhl für Biophysik (E27), Physics Departement, Technische Universität München, D-85748, Garching, Germany.
A ReitenbachCenter for Protein Assemblies (CPA) and Lehrstuhl für Biophysik (E27), Physics Departement, Technische Universität München, D-85748, Garching, Germany.
A R BauschCenter for Protein Assemblies (CPA) and Lehrstuhl für Biophysik (E27), Physics Departement, Technische Universität München, D-85748, Garching, Germany. abausch@mytum.de.ORCID 0000-0002-4608-9544

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuning colloidal structure formation is a powerful approach to building functional materials, as a wide range of optical and viscoelastic properties can be accessed by the choice of individual building blocks and their interactions. Precise control is achieved by DNA specificity, depletion forces, or geometric constraints and results in a variety of complex structures. Due to the lack of control and reversibility of the interactions, an autonomous oscillating system on a mesoscale without external driving was not feasible until now. Here, we show that tunable DNA reaction circuits controlling linker strand concentrations can drive the dynamic and fully reversible assembly of DNA-functionalized micron-sized particles. The versatility of this approach is demonstrated by programming colloidal interactions in sequential and spatial order to obtain an oscillatory structure formation process on a mesoscopic scale. The experimental results represent an approach for the development of active materials by using DNA reaction networks to scale up the dynamic control of colloidal self-organization.

Indexed as

Bacterial ProteinsColloidsDeoxyribonuclease IDNADNA-Directed DNA PolymeraseExonucleasesSynthetic BiologyBacterial ProteinsColloidsDeoxyribonuclease IDNADNA-Directed DNA PolymeraseExonucleases

Identifiers

PMID34815410
PMCPMC8611085

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.