Evidence map›Paper›PMID 37396282›Full record

ArticleACS omega2023

Dual-Role Peptide with Capping and Cleavage Site Motifs in Nanoparticle-Based One-Pot Colorimetric and Electrochemical Protease Assay.

Tamás Szabó, István Bakos, Barbara Vrbovszki, Itthipon Jeerapan, Péter Pekker, Judith Mihály, Krisztina Németh, Joseph Wang, Zsófia Keresztes

Abstract read
In one paragraph

Article in ACS omega, 2023. 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.

Tamás SzabóResearch Centre for Natural Sciences, Magyar tudósok körútja 2., 1117 Budapest, Hungary.ORCID https://orcid.org/0000-0002-9506-6410
István BakosResearch Centre for Natural Sciences, Magyar tudósok körútja 2., 1117 Budapest, Hungary.
Barbara VrbovszkiResearch Centre for Natural Sciences, Magyar tudósok körútja 2., 1117 Budapest, Hungary.
Itthipon JeerapanLaboratory of Nano-Bioelectronics, Department of Nanoengineering, Jacobs School of Engineering, University of California San Diego, La Jolla, California 92093, United States.ORCID https://orcid.org/0000-0001-8016-6411
Péter PekkerNanolab, Research Institute of Biomolecular and Chemical Engineering, University of Pannonia, Egyetem u. 10., 8200 Veszprém, Hungary.
Judith MihályResearch Centre for Natural Sciences, Magyar tudósok körútja 2., 1117 Budapest, Hungary.
Krisztina NémethResearch Centre for Natural Sciences, Magyar tudósok körútja 2., 1117 Budapest, Hungary.
Joseph WangLaboratory of Nano-Bioelectronics, Department of Nanoengineering, Jacobs School of Engineering, University of California San Diego, La Jolla, California 92093, United States.
Zsófia KeresztesResearch Centre for Natural Sciences, Magyar tudósok körútja 2., 1117 Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A new method for enzyme substrate assembly and its use in proteolytic enzyme assays with colorimetric and electrochemical detection is presented. The novelty of the method is the use of dual-function synthetic peptide containing both gold clustering and protease-sensitive moieties, which not only induces the simple formation of the peptide-decorated gold nanoparticle test substrates but also allows for the detection of proteolysis in the same batch. Protease-treated nanoparticles with a destabilized peptide shell became more prone to electroactivity, and thus, the model enzyme plasmin activity could be quantified with stripping square wave voltammetry analysis as well, giving an alternative method to conduct aggregation-based assays. Spectrophotometric and electrochemical calibration data proved to be linear within the 40-100 nM active enzyme concentration range, with possible extensions of the dynamic range by varying substrate concentration. The simple initial components and the ease of synthesis make the assay substrate preparation economic and easy to implement. The possibility of cross-check analytical results with two independent measurement techniques in the same batch greatly increases the applicability of the proposed system.

Identifiers

PMID37396282
PMCPMC10308550

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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.