Evidence map›Paper›PMID 40075560›Full record

ArticleACS applied materials & interfaces2025

Enzyme Reactions Are Accelerated or Decelerated When the Enzymes Are Located Near the DNA Nanostructure.

Peng Lin, Tomohiko Hayashi, Huyen Dinh, Eiji Nakata, Masahiro Kinoshita, Takashi Morii

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Programmable Nanoscale Motion via Molecular Patterning on DNA Origami.Angewandte Chemie (International ed. in English) · 2026
    Article
  6. 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

6 authors.

Peng LinInstitute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011, Japan.ORCID 0000-0003-2601-0787
Tomohiko HayashiInterdisciplinary Program of Biomedical Engineering, Assistive Technology, and Art and Sports Sciences, Faculty of Engineering, Niigata University, Niigata 950-2181, Japan.
Huyen DinhTam Anh Research Institute (TAMRI), Tan Binh District, Hochiminh City 72108, Vietnam.ORCID 0000-0003-0336-0362
Eiji NakataInstitute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011, Japan.ORCID 0000-0001-9564-6805
Masahiro KinoshitaGraduate School of Science, Chiba University, Chiba 263-8522, Japan.ORCID 0000-0001-8060-045X
Takashi MoriiInstitute of Advanced Energy, Kyoto University, Uji, Kyoto 611-0011, Japan.ORCID 0000-0003-3663-3267

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is known experimentally that enzymatic reactions are often accelerated when the enzymes are assembled on the scaffold of DNA nanostructures. However, the exact mechanism by which this acceleration occurs remains unclear. Here, we study the reactions of enzymes with different catalytic mechanisms assembled on a DNA scaffold with various substrates. Analysis of the hydration properties of the substrates using our accurate statistical mechanics theory classifies the substrates into two groups that behave as hydrophilic and hydrophobic solutes, respectively. The reaction of the enzyme on the DNA scaffold is accelerated with a hydrophilic substrate but decelerated with a hydrophobic substrate. We propose a mechanism of acceleration or deceleration in which, due to the formation of a high-density layer of water near the DNA surface with high negative charge density, the concentration of a substrate with high energetic affinity for water within the layer becomes higher than that near a free enzyme, whereas that of a substrate with low energetic affinity becomes lower within the layer. This study provides chemical and physical insights into a general case of biocatalysts, where the rates of chemical reactions occurring at the interface of biomolecules in aqueous environments can differ substantially from those in the bulk solution due to variations in the local concentration of a given ligand.

Indexed as

DNAEnzymesNanostructuresBiocatalysisHydrophobic and Hydrophilic InteractionsWaterDNAEnzymesWaterbiocatalystDNA scaffoldenzyme reactionhydrationinterface

Identifiers

PMID40075560
PMCPMC11912197

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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.