tetano
Editor, Senior Moderator
Biosens Bioelectron
. 2023 Jan 24;225:115101.
doi: 10.1016/j.bios.2023.115101. Online ahead of print.
Peptide nucleic acid and antifouling peptide based biosensor for the non-fouling detection of COVID-19 nucleic acid in saliva
Yanxin Li[SUP] 1 [/SUP], Shuju Zhao[SUP] 1 [/SUP], Zhenying Xu[SUP] 1 [/SUP], Xiujuan Qiao[SUP] 1 [/SUP], Mingxuan Li[SUP] 1 [/SUP], Youke Li[SUP] 1 [/SUP], Xiliang Luo[SUP] 2 [/SUP]
Affiliations
Abstract
The electrochemical biosensor with outstanding sensitivity and low cost is regarded as a viable alternative to current clinical diagnostic techniques for various disease biomarkers. However, their actual analytical use in complex biological samples is severely hampered due to the biofouling, as they are also highly sensitive to nonspecific adsorption on the sensing interfaces. Herein, we have constructed a non-fouling electrochemical biosensor based on antifouling peptides and the electroneutral peptide nucleic acid (PNA), which was used as the recognizing probe for the specific binding of the viral RNA of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Different from the negatively charged DNA probes that will normally weaken the biosensors' antifouling capabilities owing to the charge attraction of positively charged biomolecules, the neutral PNA probe will generate no side-effects on the biosensor. The biosensor demonstrated remarkable sensitivity in detecting SARS-CoV-2 viral RNA, possessing a broad linear range (1.0 fM - 1.0 nM) and a detection limit down to 0.38 fM. Furthermore, the sensing performance of the constructed electrochemical biosensor in human saliva was nearly similar to that in pure buffer, indicating satisfying antifouling capability. The combination of PNA probes with antifouling peptides offered a new strategy for the development of non-fouling sensing systems capable of assaying trace disease biomarkers in complicated biological media.
Keywords: Antifouling biosensor; Electrochemical detection; Peptide; Peptide nucleic acid; SARS-CoV-2 viral RNA.
. 2023 Jan 24;225:115101.
doi: 10.1016/j.bios.2023.115101. Online ahead of print.
Peptide nucleic acid and antifouling peptide based biosensor for the non-fouling detection of COVID-19 nucleic acid in saliva
Yanxin Li[SUP] 1 [/SUP], Shuju Zhao[SUP] 1 [/SUP], Zhenying Xu[SUP] 1 [/SUP], Xiujuan Qiao[SUP] 1 [/SUP], Mingxuan Li[SUP] 1 [/SUP], Youke Li[SUP] 1 [/SUP], Xiliang Luo[SUP] 2 [/SUP]
Affiliations
- PMID: 36708624
- DOI: 10.1016/j.bios.2023.115101
Abstract
The electrochemical biosensor with outstanding sensitivity and low cost is regarded as a viable alternative to current clinical diagnostic techniques for various disease biomarkers. However, their actual analytical use in complex biological samples is severely hampered due to the biofouling, as they are also highly sensitive to nonspecific adsorption on the sensing interfaces. Herein, we have constructed a non-fouling electrochemical biosensor based on antifouling peptides and the electroneutral peptide nucleic acid (PNA), which was used as the recognizing probe for the specific binding of the viral RNA of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Different from the negatively charged DNA probes that will normally weaken the biosensors' antifouling capabilities owing to the charge attraction of positively charged biomolecules, the neutral PNA probe will generate no side-effects on the biosensor. The biosensor demonstrated remarkable sensitivity in detecting SARS-CoV-2 viral RNA, possessing a broad linear range (1.0 fM - 1.0 nM) and a detection limit down to 0.38 fM. Furthermore, the sensing performance of the constructed electrochemical biosensor in human saliva was nearly similar to that in pure buffer, indicating satisfying antifouling capability. The combination of PNA probes with antifouling peptides offered a new strategy for the development of non-fouling sensing systems capable of assaying trace disease biomarkers in complicated biological media.
Keywords: Antifouling biosensor; Electrochemical detection; Peptide; Peptide nucleic acid; SARS-CoV-2 viral RNA.