Evidence map›Paper›PMID 41381787›Full record

ArticleMikrochimica acta2025

Bacteriophage binding receptor like-peptides and MXene-AgNPs modified label-free impedimetric biosensor for detection of Staphylococcus aureus in real samples.

Sara Asghari Dilmani, Zihni Onur Uygun, Nurullah Ciftci, Savas Tasoglu

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Article in Mikrochimica acta, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sara Asghari DilmaniSchool of Biomedical Sciences and Engineering, Koç University, 34450, Istanbul, Türkiye.
Zihni Onur UygunFaculty of Medicine, Department of Medical Biochemistry, Kafkas University, Kars, Türkiye.ORCID 0000-0001-9045-7271
Nurullah CiftciFaculty of Medicine, Department of Medical Microbiology, Kafkas University, Kars, Türkiye.ORCID 0000-0002-8934-0575
Savas TasogluSchool of Biomedical Sciences and Engineering, Koç University, 34450, Istanbul, Türkiye. stasoglu@ku.edu.tr.ORCID 0000-0003-4604-217X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This is the first report of a label-free impedimetric biosensor utilizing a bacteriophage receptor-binding protein-like peptide for the selective detection of Staphylococcus aureus (S. aureus) in clinical samples. The biosensor platform was constructed by modifying screen-printed carbon electrodes with a nanocomposite composed of MXene and silver nanoparticles (AgNPs), enabling effective immobilization of the engineered peptide sequence (CKGGGGGRHYMDQTNRHYMDQTNG). The peptide was specifically designed to preserve a key binding motif (HYMD), facilitating high-affinity interaction with S. aureus surface teichoic acids. Electrochemical impedance spectroscopy (EIS) was employed to monitor bacterial attachment through changes in charge transfer resistance. The biosensor exhibited a broad linear detection range from 10 to 10⁶ CFU/mL, with a limit of detection (LOD) of 2.78 CFU/mL. Repeatability and reproducibility tests confirmed high precision with low standard deviations across replicate measurements. Chronoimpedance analysis enabled rapid detection within approximately 7.5 min and demonstrated minimal signal interference in complex matrices such as human serum and urine. This peptide-based biosensor offers a promising, cost-effective, and portable alternative to conventional diagnostic tools for S. aureus detection. The integration of MXene-AgNP nanostructures and phage-derived recognition elements may pave the way for next-generation biosensors capable of real-time pathogen monitoring in clinical and point-of-care settings.

Indexed as

Bacteriophage ReceptorsBiosensing TechniquesMetal NanoparticlesPeptidesStaphylococcus aureusDielectric SpectroscopyElectrodesHumansLimit of DetectionNitritesSilverTransition ElementsBacteriophage ReceptorsMXeneNitritesPeptidesSilverTransition ElementsBacteriophage binding receptorBiosensorElectrochemical impedance spectroscopyMXeneScreen-printed carbon electrodeStaphylococcus aureus

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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.