Evidence map›Paper›PMID 29446165›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2018

Synthetic Transient Crosslinks Program the Mechanics of Soft, Biopolymer-Based Materials.

Jessica S Lorenz, Jörg Schnauß, Martin Glaser, Martin Sajfutdinow, Carsten Schuldt, Josef A Käs, David M Smith

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Large and stable: actin aster networks formedFrontiers in chemistry · 2022
    Article
  13. Article
  14. Review
  15. Article
  16. Actin droplet machine.Royal Society open science · 2019
    Article
  17. Computing on actin bundles network.Scientific reports · 2019
    Article
  18. Pinpointed Stimulation of EphA2 Receptors via DNA-Templated Oligovalence.International journal of molecular sciences · 2018
    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

7 authors.

Jessica S LorenzFraunhofer Institute for Cell Therapy and Immunology (IZI), 04103, Leipzig, Germany.
Jörg SchnaußFraunhofer Institute for Cell Therapy and Immunology (IZI), 04103, Leipzig, Germany.ORCID http://orcid.org/0000-0002-6408-8676
Martin GlaserFraunhofer Institute for Cell Therapy and Immunology (IZI), 04103, Leipzig, Germany.
Martin SajfutdinowFraunhofer Institute for Cell Therapy and Immunology (IZI), 04103, Leipzig, Germany.
Carsten SchuldtFraunhofer Institute for Cell Therapy and Immunology (IZI), 04103, Leipzig, Germany.
Josef A KäsPeter Debye Institute for Soft Matter Physics, Leipzig University, 04103, Leipzig, Germany.
David M SmithFraunhofer Institute for Cell Therapy and Immunology (IZI), 04103, Leipzig, Germany.ORCID http://orcid.org/0000-0002-8344-850X

Funding

European Research Council 741350
6 · The paper itself

Abstract

Actin networks are adaptive materials enabling dynamic and static functions of living cells. A central element for tuning their underlying structural and mechanical properties is the ability to reversibly connect, i.e., transiently crosslink, filaments within the networks. Natural crosslinkers, however, vary across many parameters. Therefore, systematically studying the impact of their fundamental properties like size and binding strength is unfeasible since their structural parameters cannot be independently tuned. Herein, this problem is circumvented by employing a modular strategy to construct purely synthetic actin crosslinkers from DNA and peptides. These crosslinkers mimic both intuitive and noncanonical mechanical properties of their natural counterparts. By isolating binding affinity as the primary control parameter, effects on structural and dynamic behaviors of actin networks are characterized. A concentration-dependent triphasic behavior arises from both strong and weak crosslinkers due to emergent structural polymorphism. Beyond a certain threshold, strong binding leads to a nonmonotonic elastic pulse, which is a consequence of self-destruction of the mechanical structure of the underlying network. The modular design also facilitates an orthogonal regulatory mechanism based on enzymatic cleaving. This approach can be used to guide the rational design of further biomimetic components for programmable modulation of the properties of biomaterials and cells.

Indexed as

biomimetic materialsbiopolymerscrosslinkersDNA nanotechnologymolecular design

Identifiers

PMID29446165
PMCPMC5878933

What OpenQuestion holds

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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.