Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 May 29;191(6):356.
doi: 10.1007/s00604-024-06410-4.

Chronopotentiometric sensors for antimicrobial peptide-based biosensing of Staphylococcus aureus

Affiliations

Chronopotentiometric sensors for antimicrobial peptide-based biosensing of Staphylococcus aureus

Jiarong Zhao et al. Mikrochim Acta. .

Abstract

Charged antimicrobial peptides can be used for direct potentiometric biosensing, but have never been explored. We report here a galvanostatically-controlled potentiometric sensor for antimicrobial peptide-based biosensing. Solid-state pulsed galvanostatic sensors that showed excellent stability under continuous galvanostatic polarization were prepared by utilizing reduced graphene oxide/poly (3,4-ethylenedioxythiophene): poly (4-styrenesulfonate) (rGO/PEDOT: PSS) as a solid contact. More importantly, the chronopotentiometric sensor can be made sensitive to antimicrobial peptides with intrinsic charge on demand via a current pulse. In this study, a positively charged antimicrobial peptide that can bind to Staphylococcus aureus with high affinity and good selectivity was designed as a model. Two arginine residues with positive charges were linked to the C-terminal of the peptide sequence to increase its potentiometric responses on the electrode. The bacteria binding-induced charge or charge density change of the antimicrobial peptide enables the direct chronopotentiometric detection of the target. Under the optimized conditions, the concentration of Staphylococcus aureus can be determined in the linear range 10-1.0 × 105 CFU mL-1 with a detection limit of 10 CFU mL-1. It is anticipated that such a chronopotentiometric sensing platform is readily adaptable to detect other bacteria by choosing the peptides.

Keywords: Bacteria; Biosensing; Chronopotentiometry; Ion-selective electrode; Peptide.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Bakker E, Pretsch E (2007) Modern potentiometry. Angew Chem Int Edit 46:5660–5668. https://doi.org/10.1002/anie.200605068 - DOI
    1. Hu JB, Stein A, Bühlmann P (2016) Rational design of all-solid-state ion-selective electrodes and reference electrodes. Trends Anal Chem 76:102–114. https://doi.org/10.1016/j.trac.2015.11.004 - DOI
    1. Soares RRA, Hjort RG, Pola CC, Jing DP, Cecon VS, Claussen JC, Gomes CL (2023) Ion-selective electrodes based on laser-induced graphene as an alternative method for nitrite monitoring. Microchim Acta 190:43. https://doi.org/10.1007/s00604-022-05615-9 - DOI
    1. Bakker E, Bühlmann P, Pretsch E (1997) Carrier-based ion-selective electrodes and bulk optodes. 1. General characteristics. Chem Rev 97:3083–3132. https://doi.org/10.1021/cr940394a - DOI - PubMed
    1. Bakker E (2016) Electroanalysis with membrane electrodes and liquid–liquid interfaces. Anal Chem 88:395–413. https://doi.org/10.1021/acs.analchem.5b04034 - DOI - PubMed

Publication types

MeSH terms