A universal bacterial sensor created by integrating a light modulating aptamer complex with photoelectrochemical signal readout

被引:10
|
作者
Bakhshandeh, Fatemeh [1 ]
Saha, Sudip [2 ]
Sen, Payel [1 ]
Sakib, Sadman [1 ]
MacLachlan, Roderick [1 ]
Kanji, Farhaan [1 ]
Osman, Enas [2 ]
Soleymani, Leyla [1 ,2 ,3 ]
机构
[1] Dept Engn Phys, 1280 Main St West, Hamilton, ON L8S 4L8, Canada
[2] Sch Biomed Engn, 1280 Main St West, Hamilton, ON L8S 4L8, Canada
[3] Michael G DeGroote Inst Infect Dis Res, 1280 Main St West, Hamilton, ON L8S 4L8, Canada
来源
基金
加拿大自然科学与工程研究理事会;
关键词
Aptamer; Bacterial sensing; Biosensor; Peptidoglycan; Photoelectrochemistry; CDS QUANTUM DOTS; NANOPARTICLES; IMPROVE; URINE; CELLS; WOMEN;
D O I
10.1016/j.bios.2023.115359
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Photoelectrochemical (PEC) signal transduction is of great interest for ultrasensitive biosensing; however, signalon PEC assays that do not require target labeling remain elusive. In this work, we developed a signal-on biosensor that uses nucleic acids to modulate PEC currents upon target capture. Target presence removes a biorecognition probe from a DNA duplex carrying a gold nanoparticle, bringing the gold nanoparticle in direct contact to the photoelectrode and increasing the PEC current. This assay was used to develop a universal bacterial detector by targeting peptidoglycan using an aptamer, demonstrating a limit-of-detection of 82 pg/mL (13 pM) in buffer and 239 pg/mL (37 pM) in urine for peptidoglycan and 1913 CFU/mL forEscherichia coliin urine. When challenged with a panel of unknown targets, the sensor identified samples with bacterial contamination versus fungi. The versatility of the assay was further demonstrated by analyzing DNA targets, which yielded a limit-of-detection of 372 fM.
引用
收藏
页数:9
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