Evidence map›Paper›PMID 33801952›Full record

ReviewMolecules (Basel, Switzerland)2021

Constructing Large 2D Lattices Out of DNA-Tiles.

Johannes M Parikka, Karolina Sokołowska, Nemanja Markešević, J Jussi Toppari

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Crystalline Assemblies of DNA Nanostructures and Their Functional Properties.Angewandte Chemie (International ed. in English) · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Dynamics of DNA Origami Lattices.Bioconjugate chemistry · 2023
    Review
  9. Review
  10. Review
  11. Article
  12. 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

4 authors.

Johannes M ParikkaNanoscience Center, Department of Physics, University of Jyväskylä, P.O. Box 35, 40014 Jyväskylä, Finland.
Karolina SokołowskaNanoscience Center, Department of Physics, University of Jyväskylä, P.O. Box 35, 40014 Jyväskylä, Finland.
Nemanja MarkeševićNanoscience Center, Department of Physics, University of Jyväskylä, P.O. Box 35, 40014 Jyväskylä, Finland.
J Jussi ToppariNanoscience Center, Department of Physics, University of Jyväskylä, P.O. Box 35, 40014 Jyväskylä, Finland.ORCID 0000-0002-1698-5591

Funding

Jane ja Aatos Erkon Säätiö 2019
6 · The paper itself

Abstract

The predictable nature of deoxyribonucleic acid (DNA) interactions enables assembly of DNA into almost any arbitrary shape with programmable features of nanometer precision. The recent progress of DNA nanotechnology has allowed production of an even wider gamut of possible shapes with high-yield and error-free assembly processes. Most of these structures are, however, limited in size to a nanometer scale. To overcome this limitation, a plethora of studies has been carried out to form larger structures using DNA assemblies as building blocks or tiles. Therefore, DNA tiles have become one of the most widely used building blocks for engineering large, intricate structures with nanometer precision. To create even larger assemblies with highly organized patterns, scientists have developed a variety of structural design principles and assembly methods. This review first summarizes currently available DNA tile toolboxes and the basic principles of lattice formation and hierarchical self-assembly using DNA tiles. Special emphasis is given to the forces involved in the assembly process in liquid-liquid and at solid-liquid interfaces, and how to master them to reach the optimum balance between the involved interactions for successful self-assembly. In addition, we focus on the recent approaches that have shown great potential for the controlled immobilization and positioning of DNA nanostructures on different surfaces. The ability to position DNA objects in a controllable manner on technologically relevant surfaces is one step forward towards the integration of DNA-based materials into nanoelectronic and sensor devices.

Indexed as

DNANanostructuresNanotechnologyDNAcomplexityDNA nanotechnologyDNA origamiDNA self-assemblyhierarchylatticelithography

Identifiers

PMID33801952
PMCPMC8000633

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.