2013
DOI: 10.1016/j.ab.2013.01.014
|View full text |Cite
|
Sign up to set email alerts
|

Isolation and characterization of DNA aptamers against Escherichia coli using a bacterial cell–systematic evolution of ligands by exponential enrichment approach

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
53
0

Year Published

2015
2015
2024
2024

Publication Types

Select...
5
2
1

Relationship

1
7

Authors

Journals

citations
Cited by 101 publications
(58 citation statements)
references
References 36 publications
1
53
0
Order By: Relevance
“…The best performance is attributed to the Ag@Au-aptasensor and there is a linear relationship between peak current and the concentration of E. coli to 10 4 CFU/mL. For higher concentrations, the current no longer changes significantly because of the saturation of the surface [29]. The calculated LOD for this aptasensor is around 90 CFU/mL, while the reported LOD in the literature for this aptamer cocktail is 370 CFU/mL at the surface of a gold electrode [28].…”
Section: Electrochemical Detection Of E Coli and The Role Of Ag@au Nmentioning
confidence: 82%
“…The best performance is attributed to the Ag@Au-aptasensor and there is a linear relationship between peak current and the concentration of E. coli to 10 4 CFU/mL. For higher concentrations, the current no longer changes significantly because of the saturation of the surface [29]. The calculated LOD for this aptasensor is around 90 CFU/mL, while the reported LOD in the literature for this aptamer cocktail is 370 CFU/mL at the surface of a gold electrode [28].…”
Section: Electrochemical Detection Of E Coli and The Role Of Ag@au Nmentioning
confidence: 82%
“…However, due to outer cell surface complexity, molecular level understanding of how these aptamers bind on E. coli strains is still unknown. Using, the same aptamers could bind to cell surface components competitively followed by fluorescence emission; therefore, two or more different aptamers could be assumed to bind non-competitively (Kim et al 2013c). …”
Section: Escherichia Colimentioning
confidence: 99%
“…Cell-SELEX provides flexibility in the detection of various cell types (bacteria, viruses, cancer cells) and is now used in the identification of the unknown cells' surface biomarkers (Kim et al 2013c). Recently, modified SELEX protocols based on traditional SELEX method have significantly improved to advance the application of aptamer technology in various fields (Xu et al 2011).…”
Section: Introductionmentioning
confidence: 99%
“…The FNP had excitation and emission maxima of 540 and 560 nm, respectively. Next, our previously described 3′-amino-modified E. coli-specific aptamer (5′-GCA ATG GTA CGG TAC TTC CCC ATG AGT GTT GTG AAA TGT TGG GAC ACT AGG TGG CAT AGA GCC GCA AAA GTG CAC GCT ACT TTG CTA A-3′) was added to the solution at a final concentration of 750 nM (Kim et al, 2013). The resulting mixture was incubated at room temperature for an additional 3 h in a ThermoMixer (Eppendorf, Germany) to allow time for the conjugation of aptamers to microspheres.…”
Section: Preparation Of A-fnpsmentioning
confidence: 99%
“…We used an E. colispecific ssDNA aptamer, which we described in a previous study and which had a dissociation constant of 25.2 nM for E. coli (Kim et al, 2013). A-FNPs were analyzed by DLS to clarify whether they dispersed well or aggregate in solution.…”
Section: A-fnps For E Coli Detectionmentioning
confidence: 99%