Evidence map›Paper›PMID 40661195›Full record

ArticleRSC advances2025

Toward high-density streptavidin arrays on DNA origami nanostructures.

Lukas Rabbe, Emilia Tomm, Guido Grundmeier, Adrian Keller

Abstract read
In one paragraph

Article in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Two-dimensional data storage using a DNA molecular register.Frontiers in bioengineering and biotechnology · 2026
    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.

Lukas RabbePaderborn University, Technical and Macromolecular Chemistry Warburger Str. 100 33098 Paderborn Germany adrian.keller@uni-paderborn.de.
Emilia TommPaderborn University, Technical and Macromolecular Chemistry Warburger Str. 100 33098 Paderborn Germany adrian.keller@uni-paderborn.de.
Guido GrundmeierPaderborn University, Technical and Macromolecular Chemistry Warburger Str. 100 33098 Paderborn Germany adrian.keller@uni-paderborn.de.
Adrian KellerPaderborn University, Technical and Macromolecular Chemistry Warburger Str. 100 33098 Paderborn Germany adrian.keller@uni-paderborn.de.ORCID https://orcid.org/0000-0001-7139-3110

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The binding of the protein streptavidin (SAv) to biotin-modified DNA origami nanostructures (DONs) is widely employed in the single-molecule study of chemical reactions, the arrangement of functional proteins and nanomaterials with molecular precision, and numerous instances of DON-based cryptography, steganography, and computing. The latter application areas in particular would benefit from high-density SAv arrays to achieve higher information densities. The finite size and tetrameric nature of SAv, however, pose certain limits to the SAv density that can be achieved in such arrays. In this work, we explore these limits by investigating the impact of selected design factors and environmental conditions on SAv binding to DON-supported biotin arrays. We identify the optimal distance between neighboring binding sites and the optimal length of the single-stranded spacer between DON surface and biotin modification. This allows us to assemble a 2D SAv array composed of 20 biotin modifications arranged at a density of about 0.008 nm

Identifiers

PMID40661195
PMCPMC12257290

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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.