Split aptamer mediated endonuclease amplification for small-molecule detection

2015 ◽  
Vol 51 (20) ◽  
pp. 4196-4199 ◽  
Author(s):  
Qing Li ◽  
Yan-Dan Wang ◽  
Guo-Li Shen ◽  
Hao Tang ◽  
Ru-Qin Yu ◽  
...  

A novel, highly sensitive split aptamer mediated endonuclease amplification strategy for the construction of aptameric sensors is reported.

The Analyst ◽  
2021 ◽  
Author(s):  
Ahmed Mohamed ◽  
Ryan Walsh ◽  
Mohamed Cherif ◽  
Hassan A. Hafez ◽  
Xavier Ropagnol ◽  
...  

We demonstrate the rapid and highly sensitive detection of a small molecule, microcystin-LR (MC-LR) toxin using an aptasensor based on a terahertz (THz) emission technique named the terahertz chemical microscope (TCM).


2017 ◽  
Vol 97 ◽  
pp. 292-298 ◽  
Author(s):  
Jin-Ho Park ◽  
Ju-Young Byun ◽  
Hyungjun Jang ◽  
Donggu Hong ◽  
Min-Gon Kim

2021 ◽  
Vol 351 ◽  
pp. 129270
Author(s):  
Yuchen Bai ◽  
Yahui Wang ◽  
Qiang Li ◽  
Leina Dou ◽  
Minggang Liu ◽  
...  

The Analyst ◽  
2021 ◽  
Vol 146 (8) ◽  
pp. 2679-2688
Author(s):  
Chammari Pothipor ◽  
Noppadol Aroonyadet ◽  
Suwussa Bamrungsap ◽  
Jaroon Jakmunee ◽  
Kontad Ounnunkad

An ultrasensitive electrochemical biosensor based on a gold nanoparticles/graphene/polypyrrole composite modified electrode and a signal amplification strategy employing methylene blue is developed as a potential tool for the detection of miRNA-21.


RSC Advances ◽  
2014 ◽  
Vol 4 (51) ◽  
pp. 27091-27097 ◽  
Author(s):  
Qingwang Xue ◽  
Yanqin Lv ◽  
Yuanfu Zhang ◽  
Shuling Xu ◽  
Qiaoli Yue ◽  
...  

A novel label-free amplified fluorescent sensing scheme based on target-responsive dumbbell probe-mediated rolling circle amplification (D-RCA) has been developed for sensitive and selective detection of mercuric ions.


2020 ◽  
Author(s):  
Rhushabh Maugi ◽  
bernadette gamble ◽  
david bunka ◽  
Mark Platt

A universal aptamer-based sensing strategy is proposed using DNA modified nanocarriers and Resistive Pulse Sensing for the rapid and label free detection of small molecules. The surface of a magnetic nanocarrier was first modified with a ssDNA aka linker which is designed to be partially complimentary in sequence to a ssDNA aptamer. The aptamer and linker form a stable dsDNA complex on the nanocarriers surface. Upon the addition of the target molecule, a conformational change takes place where the aptamer preferentially binds to the target over the linker; causing the aptamer to be released into solution. The RPS measures the change in velocity of the nanocarrier as its surface changes from dsDNA to ssDNA, and its velocity is used as a proxy for the concentration of the target. We illustrate the versatility of the assay by demonstrating the detection of the antibiotic Moxifloxacin, and chemotherapeutics Imatinib and Irinotecan.


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