scholarly journals Multiplex single-molecule DNA barcoding using an oligonucleotide ligation assay

2018 ◽  
Author(s):  
Ivo Severins ◽  
Malwina Szczepaniak ◽  
Chirlmin Joo

Detection of specific nucleic acid sequences is invaluable in biological studies such as genetic disease diagnostics and genome profiling. Here we developed a highly sensitive and specific detection method that combines an advanced oligonucleotide ligation assay (OLA) with multicolor single-molecule fluorescence. We demonstrated that 7-nt long DNA barcodes have the optimal short length to ascertain specificity while being long enough for sufficient ligation. Using four spectrally separated fluorophores to label DNA barcodes, we simultaneously distinguished four DNA target sequences differing by only a single nucleotide. Our new single-molecule approach will allow for accurate identification of low abundance molecules without the need for target DNA pre-amplification.

2016 ◽  
Vol 8 (40) ◽  
pp. 7413-7419 ◽  
Author(s):  
Min Huang ◽  
Hanying Li ◽  
Hanping He ◽  
Xiuhua Zhang ◽  
Shengfu Wang

A simple EIS sensor was developed for the highly sensitive and specific detection of G–G mismatches in dsDNA using a small molecule-modified gold electrode. Recognition and detection were achieved by ΔRct before and after incubation with target DNA.


2018 ◽  
Vol 10 (37) ◽  
pp. 4596-4603
Author(s):  
Joong Hyun Kim ◽  
Chan Ho Chung

Isothermal control of target–probe interaction using graphene oxide and RNase H allows highly sensitive and specific detection of target DNA.


2015 ◽  
Vol 51 (20) ◽  
pp. 4220-4222 ◽  
Author(s):  
Chenyang Tao ◽  
Yurong Yan ◽  
Hua Xiang ◽  
Dan Zhu ◽  
Wei Cheng ◽  
...  

Schematic representation of the designed strategy for target DNA detection.


Author(s):  
Xiaojia Jiang ◽  
Mingsong Zang ◽  
Fei Li ◽  
Chunxi Hou ◽  
Quan Luo ◽  
...  

Biological nanopore-based techniques have attracted more and more attention recently in the field of single-molecule detection, because they allow the real-time, sensitive, high-throughput analysis. Herein, we report an engineered biological...


Nano Letters ◽  
2021 ◽  
Vol 21 (4) ◽  
pp. 1694-1701 ◽  
Author(s):  
Sung Hyun Kim ◽  
Hyunwoo Kim ◽  
Hawoong Jeong ◽  
Tae-Young Yoon

2017 ◽  
Vol 8 (5) ◽  
pp. 3668-3675 ◽  
Author(s):  
Ruijie Deng ◽  
Kaixiang Zhang ◽  
Yupeng Sun ◽  
Xiaojun Ren ◽  
Jinghong Li

We report a robust method for the efficient imaging of mRNA with single-nucleotide and near-single-molecule resolution in single cells.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Jiao Fan ◽  
Yige Ding ◽  
Chao Ren ◽  
Ziguo Song ◽  
Jie Yuan ◽  
...  

AbstractCytosine or adenine base editors (CBEs or ABEs) hold great promise in therapeutic applications because they enable the precise conversion of targeted base changes without generating of double-strand breaks. However, both CBEs and ABEs induce substantial off-target DNA editing, and extensive off-target RNA single nucleotide variations in transfected cells. Therefore, the potential effects of deaminases induced by DNA base editors are of great importance for their clinical applicability. Here, the transcriptome-wide deaminase effects on gene expression and splicing is examined. Differentially expressed genes (DEGs) and differential alternative splicing (DAS) events, induced by base editors, are identified. Both CBEs and ABEs generated thousands of DEGs and hundreds of DAS events. For engineered CBEs or ABEs, base editor-induced variants had little effect on the elimination of DEGs and DAS events. Interestingly, more DEGs and DAS events are observed as a result of over expressions of cytosine and adenine deaminases. This study reveals a previously overlooked aspect of deaminase effects in transcriptome-wide gene expression and splicing, and underscores the need to fully characterize such effects of deaminase enzymes in base editor platforms.


2017 ◽  
Vol 117 (2) ◽  
pp. 447-451 ◽  
Author(s):  
Marijo Parčina ◽  
Ingrid Reiter-Owona ◽  
Frank P. Mockenhaupt ◽  
Valerija Vojvoda ◽  
Jean Bosco Gahutu ◽  
...  

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