A Novel PCR-Free Ultrasensitive GQD-Based Label-Free Electrochemical DNA Sensor for Sensitive and Rapid Detection of Francisella tularensis

被引:0
|
作者
Savas, Sumeyra [1 ]
Saricam, Melike [2 ]
机构
[1] Bandirma Onyedi Eylul Univ, Med Sch, Dept Clin Microbiol, TR-10200 Bandirma, Turkiye
[2] Sci & Technol Res Council Turkiye TUBITAK, Marmara Res Ctr, CBRN Def Technol R&D Grp, Mat & Proc Technol, TR-41470 Kocaeli, Turkiye
关键词
DNA biosensor; Francisella tularensis; graphene quantum dots; infection disease; label-free biosensor; DIFFERENTIAL-PULSE VOLTAMMETRY; GRAPHENE QUANTUM DOTS; CHARGE-TRANSFER; GOLD NANOPARTICLE; BIOSENSOR; ELECTRODE; TULAREMIA; PROTEINS; PLATFORM; ANTIGEN;
D O I
10.3390/mi15111308
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Biological warfare agents are infectious microorganisms or toxins capable of harming or killing humans. Francisella tularensis is a potential bioterrorism agent that is highly infectious, even at very low doses. Biosensors for biological warfare agents are simple yet reliable point-of-care analytical tools. Developing highly sensitive, reliable, and cost-effective label-free DNA biosensors poses significant challenges, particularly when utilizing traditional techniques such as fluorescence, electrochemical methods, and others. These challenges arise primarily due to the need for labeling, enzymes, or complex modifications, which can complicate the design and implementation of biosensors. In this study, we fabricated Graphene Quantum dot (GQD)-functionalized biosensors for highly sensitive label-free DNA detection. GQDs were immobilized on the surface of screen-printed gold electrodes via mercaptoacetic acid with a thiol group. The single-stranded DNA (ssDNA) probe was also immobilized on GQDs through strong pi-pi interactions. The ssDNA probe can hybridize with the ssDNA target and form double-stranded DNA, leading to a decrease in the effect of GQD but a positive shift associated with the increase in DNA concentration. The specificity of the developed system was observed with different microorganism target DNAs and up to three-base mismatches in the target DNA, effectively distinguishing the target DNA. The response time for the target DNA molecule is approximately 1010 s (17 min). Experimental steps were monitored using UV/Vis spectroscopy, Atomic Force Microscopy (AFM), and electrochemical techniques to confirm the successful fabrication of the biosensor. The detection limit can reach 0.1 nM, which is two-five orders of magnitude lower than previously reported methods. The biosensor also exhibits a good linear range from 105 to 0.01 nM and has good specificity. The biosensor's detection limit (LOD) was evaluated as 0.1 nM from the standard calibration curve, with a correlation coefficient of R2 = 0.9712, showing a good linear range and specificity. Here, we demonstrate a cost-effective, GQD-based SPGE/F. tularensis DNA test suitable for portable electrochemical devices. This application provides good perspectives for point-of-care portable electrochemical devices that integrate sample processing and detection into a single cartridge without requiring a PCR before detection. Based on these results, it can be concluded that this is the first enzyme-free electrochemical DNA biosensor developed for the rapid and sensitive detection of F. tularensis, leveraging the nanoenzyme and catalytic properties of GQDs.
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页数:20
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