Evidence map›Paper›PMID 42461555›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Immobilization of Enzyme Cascades with DNA Scaffolds.

Le Minh Bui, Huong Thi Thu Phung, Khiem V Nguyen

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 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

3 authors.

Le Minh BuiNTT Hi-Tech Institute, Nguyen Tat Thanh University, Ho Chi Minh City, Vietnam.
Huong Thi Thu PhungNTT Hi-Tech Institute, Nguyen Tat Thanh University, Ho Chi Minh City, Vietnam.
Khiem V NguyenNTT Hi-Tech Institute, Nguyen Tat Thanh University, Ho Chi Minh City, Vietnam. nvkhiem@ntt.edu.vn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biofuel cells (BFCs) have been gaining popularity as a means of harvesting energy from renewable fuel sources. Even though a wide variety of BFC types have been developed, enzymatic biofuel cells (EBFCs) that employ enzymes as biocatalysts have become appealing technologies due to their ability to convert chemical energy stored in organic substrates into electrical energy with high turnover rates and easy control over the system. However, the commercial feasibility of EBFCs has been hampered by the poor energy density caused by the partial oxidation of fuels. The utilization of multi-enzyme cascades to perform sequential oxidation of fuels is an attractive approach to enhance the energy density of EBFCs. Nevertheless, the mass transport of intermediates between enzymes is a limiting factor of these enzyme systems. DNA scaffolds offer a suitable approach to partly overcome this obstacle as they allow for the precise control of enzyme arrangements, which facilitates the timely interaction of reaction intermediates and enzymes in close proximity. In this chapter, we describe protocols for the assembly of an invertase (Inv)/glucose oxidase (GOx) enzyme cascade on a DNA scaffold and the preparation of a bioanode using the assembled enzyme-DNA complex for improved bioelectrocatalysis.

Indexed as

beta-FructofuranosidaseBioelectric Energy SourcesDNAEnzymes, ImmobilizedGlucose OxidaseBiocatalysisDNA NanostructuresOxidation-Reductionbeta-FructofuranosidaseDNAEnzymes, ImmobilizedGlucose OxidaseBiofuel cellDNA scaffoldEnzyme cascadeGlucose oxidaseInvertase

Identifiers

PMID42461555

What OpenQuestion holds

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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.