Evidence map›Paper›PMID 31467979›Full record

ArticleScience advances2019

Exploiting mammalian low-complexity domains for liquid-liquid phase separation-driven underwater adhesive coatings.

Mengkui Cui, Xinyu Wang, Bolin An, Chen Zhang, Xinrui Gui, Ke Li, Yingfeng Li, Peng Ge, Junhu Zhang, Cong Liu and 1 more

Abstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
  2. Review
  3. A biofilm-derived peptide as an underwater adhesive.bioRxiv : the preprint server for biology · 2026
    Article
  4. Physics-guided design of intrinsically disordered proteins.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Review
  7. Review
  8. Bioinspired functional materials for biomedical applications.Frontiers in bioengineering and biotechnology · 2026
    Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
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  17. Review
  18. Article
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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

11 authors.

Mengkui CuiMaterials and Physical Biology Division, School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0001-5466-5348
Xinyu WangMaterials and Physical Biology Division, School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Bolin AnMaterials and Physical Biology Division, School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Chen ZhangMaterials and Physical Biology Division, School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0003-1468-2906
Xinrui GuiUniversity of Chinese Academy of Sciences, Beijing 100049, China.
Ke LiMaterials and Physical Biology Division, School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Yingfeng LiMaterials and Physical Biology Division, School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Peng GeState Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, China.
Junhu ZhangState Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, China.ORCID 0000-0001-9100-6608
Cong LiuInterdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China.ORCID 0000-0003-3425-6672
Chao ZhongMaterials and Physical Biology Division, School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.ORCID 0000-0002-6638-3652

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many biological materials form via liquid-liquid phase separation (LLPS), followed by maturation into a solid-like state. Here, using a biologically inspired assembly mechanism designed to recapitulate these sequential assemblies, we develop ultrastrong underwater adhesives made from engineered proteins containing mammalian low-complexity (LC) domains. We show that LC domain-mediated LLPS and maturation substantially promotes the wetting, adsorption, priming, and formation of dense, uniform amyloid nanofiber coatings on diverse surfaces (e.g., Teflon), and even penetrating difficult-to-access locations such as the interiors of microfluidic devices. Notably, these coatings can be deposited on substrates over a broad range of pH values (3 to 11) and salt concentrations (up to 1 M NaCl) and exhibit strong underwater adhesion performance. Beyond demonstrating the utility of mammalian LC domains for driving LLPS in soft materials applications, our study illustrates a powerful example of how combining LLPS with subsequent maturation steps can be harnessed for engineering protein-based materials.

Identifiers

PMID31467979
PMCPMC6707783

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Registered trials

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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.