Evidence map›Paper›PMID 40837052›Full record

ArticleSmall science2025

Immobilization of Enzyme-Polymer Hybrids and Nanozymes Through Electrostatic Interactions: Toward Multicatalytic Microreactors with Controlled Nanoarchitecture.

Aitor Ontoria, Irene Alonso-Sampedro, Yixuan Yan, Ayşe Latif, Ben F Spencer, Aitor Larrañaga, Ana Beloqui, Christos Tapeinos

Abstract read
In one paragraph

Article in Small science, 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. 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

8 authors.

Aitor OntoriaPOLYMAT and Department of Applied Chemistry University of the Basque Country (UPV/EHU) Donostia-San Sebastián 20018 Spain.ORCID https://orcid.org/0009-0001-6926-9759
Irene Alonso-SampedroPOLYMAT and Department of Applied Chemistry University of the Basque Country (UPV/EHU) Donostia-San Sebastián 20018 Spain.
Yixuan YanDivision of Pharmacy and Optometry Faculty of Biology, Medicine and Health University of Manchester Stopford Building, Oxford Road Manchester M13 9PT UK.
Ayşe LatifDivision of Pharmacy and Optometry Faculty of Biology, Medicine and Health University of Manchester Stopford Building, Oxford Road Manchester M13 9PT UK.ORCID https://orcid.org/0000-0002-7245-8729
Ben F SpencerDepartment of Materials and Henry Royce Institute The University of Manchester Oxford Road Manchester M13 9PL UK.ORCID https://orcid.org/0000-0002-1453-5327
Aitor LarrañagaDepartment of Mining-Metallurgy Engineering and Materials Science POLYMAT Bilbao School of Engineering University of the Basque Country (UPV/EHU) Plaza Torres Quevedo 1 Bilbao 48013 Spain.ORCID https://orcid.org/0000-0002-2123-6069
Ana BeloquiPOLYMAT and Department of Applied Chemistry University of the Basque Country (UPV/EHU) Donostia-San Sebastián 20018 Spain.ORCID https://orcid.org/0000-0002-7693-4163
Christos TapeinosDivision of Pharmacy and Optometry Faculty of Biology, Medicine and Health University of Manchester Stopford Building, Oxford Road Manchester M13 9PT UK.ORCID https://orcid.org/0000-0001-8192-6750

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The optimal allocation of catalysts and their precise compartmentalization are vital to ensure efficient cascade reactions. The layer-by-layer approach offers the possibility of assembling various building blocks onto templates of different sizes and shapes, thus representing a powerful tool for fabricating multicatalytic reactors with controlled nanoarchitecture. However, this process usually relies on electrostatic interactions between building blocks, which means a limitation when working with natural enzymes. Accordingly, both the loading capacity and control over membrane architecture are compromised by the inherent surface charge of the enzymes. Here, this study introduces a modular strategy to assemble engineered enzyme-polymer hybrids and inorganic nanozymes onto colloidal templates, giving rise to multicatalytic reactors. The surface charge of the engineered enzyme-polymer hybrids can be finely tuned, allowing their à-la-carte assembly into multilayer membranes. Following this approach, the distance between catalytic units and their arrangement on colloidal templates at the nano- and micrometer scale can be precisely controlled, resulting in optimized configurations with enhanced cascade efficiency. The synthesized multicatalytic reactors can reduce the metabolic activity of human pancreatic stellate cells, confirming their functional activity in biological microenvironments and highlighting their potential for biomedical applications.

Indexed as

CaCO3 templated assembliescompartmentalized enzymatic cascadeslayer‐by‐layerMn3O4 nanozymesmultilayer microreactors

Identifiers

PMID40837052
PMCPMC12362757

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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.