Evidence map›Paper›PMID 42144778›Full record

ArticleACS synthetic biology2026

Systematic Exploration of Synthesis and Function Landscapes for DNA Hydrogels.

Mihane Kawada, Katsunori Aizawa, Kazumasa Ohtake, Hiromi Nakata, Yosuke Ochi, Ryusei Matsumoto, Daisuke Kiga, Tomoaki Matsuura, Shogo Hamada

Abstract read
In one paragraph

Article in ACS synthetic biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Mihane KawadaDepartment of Systems and Control Engineering, School of Engineering, Institute of Science Tokyo, Yokohama, Kanagawa 226-8501, Japan.
Katsunori AizawaDepartment of Computer Science, School of Computing, Institute of Science Tokyo, Yokohama, Kanagawa 226-8501, Japan.
Kazumasa OhtakeDepartment of Electrical Engineering and Bioscience, School of Advanced Science and Engineering, Waseda University, Shinjuku-ku, Tokyo 162-8480, Japan.
Hiromi NakataThe Smart Life Science Institute, Advanced Collaborative Research Organization for Smart Society, Waseda University, Shinjuku-ku, Tokyo 169-8050, Japan.
Yosuke OchiDepartment of Computer Science, School of Computing, Institute of Science Tokyo, Yokohama, Kanagawa 226-8501, Japan.
Ryusei MatsumotoDepartment of Life Science and Technology, School of Life Science and Technology, Institute of Science Tokyo, Meguro-ku, Tokyo 152-8550, Japan.
Daisuke KigaDepartment of Electrical Engineering and Bioscience, School of Advanced Science and Engineering, Waseda University, Shinjuku-ku, Tokyo 162-8480, Japan.ORCID 0000-0003-3778-5887
Tomoaki MatsuuraEarth-Life Science Institute, Institute of Science Tokyo, Meguro-ku, Tokyo 152-8550, Japan.ORCID 0000-0003-1015-6781
Shogo HamadaDepartment of Systems and Control Engineering, School of Engineering, Institute of Science Tokyo, Yokohama, Kanagawa 226-8501, Japan.ORCID 0000-0003-1910-0581

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmable biomaterials enable the control of macroscopic material properties through molecular-level design. DNA hydrogels are particularly promising among various biomolecular materials because their sequence design can be directly translated into material functionality. Rolling circle amplification (RCA) enables the fabrication of DNA hydrogels while densely encoding functional sequences such as aptamers. However, the rational design of functional RCA-based DNA hydrogels remains challenging due to the vast, interdependent space of synthesis and sequence parameters. Here we present an exploration framework using an acoustic liquid handler to systematically map both synthesis conditions and aptamer sequences. Systematic exploration across 90 synthesis conditions (270 samples) revealed the multidimensional synthesis landscape of RCA-based DNA hydrogels and identified key parameters contributing to robust gel formation. In addition, systematic sequence mapping of 96 aptamer variants (288 samples) enabled efficient discovery of color-specific aptameric mutants for functional implementation in the hydrogel. By integrating material synthesis and functional sequence exploration, this framework provides a useful strategy for accelerating the rational design of functional DNA-based materials.

Indexed as

DNAHydrogelsAptamers, NucleotideNucleic Acid Amplification TechniquesAptamers, NucleotideDNAHydrogelsaptamerbottom-up designDNA hydrogelprogrammable biomaterialrolling circle amplificationsemihigh throughput handling

Identifiers

PMID42144778
PMCPMC13288893

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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.