Evidence map›Paper›PMID 30150392›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Multivalent, multiflavored droplets by design.

Yin Zhang, Xiaojin He, Rebecca Zhuo, Ruojie Sha, Jasna Brujic, Nadrian C Seeman, Paul M Chaikin

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. DNA self-organization controls valence in programmable colloid design.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Article
  12. Colloidal metallurgy.Nature chemistry · 2021
    Article
  13. Photo-printing of faceted DNA patchy particles.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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.

Yin ZhangPhysics Department, Center for Soft Matter Research, New York University, New York, NY 10003; yin.zhang@nyu.edu xiaojin.he@nyu.edu ned.seeman@nyu.edu chaikin@nyu.edu.
Xiaojin HePhysics Department, Center for Soft Matter Research, New York University, New York, NY 10003; yin.zhang@nyu.edu xiaojin.he@nyu.edu ned.seeman@nyu.edu chaikin@nyu.edu.
Rebecca ZhuoPhysics Department, Center for Soft Matter Research, New York University, New York, NY 10003.
Ruojie ShaChemistry Department, New York University, New York, NY 10003.
Jasna BrujicPhysics Department, Center for Soft Matter Research, New York University, New York, NY 10003.
Nadrian C SeemanChemistry Department, New York University, New York, NY 10003 yin.zhang@nyu.edu xiaojin.he@nyu.edu ned.seeman@nyu.edu chaikin@nyu.edu.
Paul M ChaikinPhysics Department, Center for Soft Matter Research, New York University, New York, NY 10003; yin.zhang@nyu.edu xiaojin.he@nyu.edu ned.seeman@nyu.edu chaikin@nyu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nature self-assembles functional materials by programming flexible linear arrangements of molecules and then folding them to make 2D and 3D objects. To understand and emulate this process, we have made emulsion droplets with specific recognition and controlled valence. Uniquely monovalent droplets form dimers: divalent lead to polymer-like chains, trivalent allow for branching, and programmed mixtures of different valences enable a variety of designed architectures and the ability to subsequently close and open structures. Our functional building blocks are a hybrid of micrometer-scale emulsion droplets and nanoscale DNA origami technologies. Functional DNA origami rafts are first added to droplets and then herded into a patch using specifically designated "shepherding" rafts. Additional patches with the same or different specificities can be formed on the same droplet, programming multiflavored, multivalence droplets. The mobile patch can bind to a patch on another droplet containing complementary functional rafts, leading to primary structure formation. Further binding of nonneighbor droplets can produce secondary structures, a third step in hierarchical self-assembly. The use of mobile patches rather than uniform DNA coverage has the advantage of valence control at the expense of slow kinetics. Droplets with controlled flavors and valences enable a host of different material and device architectures.

Indexed as

DNA origamipatchy particleself-assembly

Identifiers

PMID30150392
PMCPMC6140528

What OpenQuestion holds

Textmetadata
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.