Functional nucleic acids for detecting bacteria

Bacterial infection represents one of the leading causes of disease and death, and as such, bacterial detection is an important step in managing infectious diseases. The current protocol requires growing cell cultures, which can take several days. Fast detection of low copies of bacterial cells has...

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Main Authors: Huang Po-Jung Jimmy, Liu Minchuan, Liu Juewen
Format: Article
Language:English
Published: De Gruyter 2013-02-01
Series:Reviews in Analytical Chemistry
Subjects:
Online Access:https://doi.org/10.1515/revac-2012-0027
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spelling doaj-e245c28df6ed4267ab9297f2b293769a2021-09-05T14:00:13ZengDe GruyterReviews in Analytical Chemistry0793-01352191-01892013-02-01321778910.1515/revac-2012-0027Functional nucleic acids for detecting bacteriaHuang Po-Jung Jimmy0Liu MinchuanLiu JuewenDepartment of Chemistry and Waterloo Institute for Nanotechnology, University of Waterloo, Waterloo, Ontario, N2L 3G1 CanadaBacterial infection represents one of the leading causes of disease and death, and as such, bacterial detection is an important step in managing infectious diseases. The current protocol requires growing cell cultures, which can take several days. Fast detection of low copies of bacterial cells has thus posed an analytical challenge. Among the new strategies developed to achieve this goal, functional nucleic acids (FNAs) have emerged to be a promising platform. FNAs include DNAzymes, aptamers, and aptazymes, all of which can recognize analytes other than complementary nucleic acids. FNAs are obtained using a combinatorial biology technique called systematic evolution of ligands by exponential enrichment (SELEX). FNAs have been isolated against not only purified proteins and surface markers from bacterial cells but also whole cells. A diverse range of signaling mechanisms including fluorescence, color, and electrochemistry-based detection has been reported. Although the majority of current sensors cannot achieve single-cell sensitivity, with improved combinatorial selection techniques and the incorporation of nanomaterials to realize multivalent binding and signal amplification, FNAs represent a feasible solution for bacterial detection.https://doi.org/10.1515/revac-2012-0027aptamersbacteriabiosensorsfluorescence
collection DOAJ
language English
format Article
sources DOAJ
author Huang Po-Jung Jimmy
Liu Minchuan
Liu Juewen
spellingShingle Huang Po-Jung Jimmy
Liu Minchuan
Liu Juewen
Functional nucleic acids for detecting bacteria
Reviews in Analytical Chemistry
aptamers
bacteria
biosensors
fluorescence
author_facet Huang Po-Jung Jimmy
Liu Minchuan
Liu Juewen
author_sort Huang Po-Jung Jimmy
title Functional nucleic acids for detecting bacteria
title_short Functional nucleic acids for detecting bacteria
title_full Functional nucleic acids for detecting bacteria
title_fullStr Functional nucleic acids for detecting bacteria
title_full_unstemmed Functional nucleic acids for detecting bacteria
title_sort functional nucleic acids for detecting bacteria
publisher De Gruyter
series Reviews in Analytical Chemistry
issn 0793-0135
2191-0189
publishDate 2013-02-01
description Bacterial infection represents one of the leading causes of disease and death, and as such, bacterial detection is an important step in managing infectious diseases. The current protocol requires growing cell cultures, which can take several days. Fast detection of low copies of bacterial cells has thus posed an analytical challenge. Among the new strategies developed to achieve this goal, functional nucleic acids (FNAs) have emerged to be a promising platform. FNAs include DNAzymes, aptamers, and aptazymes, all of which can recognize analytes other than complementary nucleic acids. FNAs are obtained using a combinatorial biology technique called systematic evolution of ligands by exponential enrichment (SELEX). FNAs have been isolated against not only purified proteins and surface markers from bacterial cells but also whole cells. A diverse range of signaling mechanisms including fluorescence, color, and electrochemistry-based detection has been reported. Although the majority of current sensors cannot achieve single-cell sensitivity, with improved combinatorial selection techniques and the incorporation of nanomaterials to realize multivalent binding and signal amplification, FNAs represent a feasible solution for bacterial detection.
topic aptamers
bacteria
biosensors
fluorescence
url https://doi.org/10.1515/revac-2012-0027
work_keys_str_mv AT huangpojungjimmy functionalnucleicacidsfordetectingbacteria
AT liuminchuan functionalnucleicacidsfordetectingbacteria
AT liujuewen functionalnucleicacidsfordetectingbacteria
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