Toward Non-Enzymatic Ultrasensitive Identification of Single Nucleotide Polymorphisms by Optical Methods

Single nucleotide polymorphisms (SNPs) are single nucleotide variations which comprise the most wide spread source of genetic diversity in the genome. Currently, SNPs serve as markers for genetic predispositions, clinically evident disorders and diverse drug responses. Present SNP diagnostics are pr...

Full description

Bibliographic Details
Main Author: Kira Astakhova
Format: Article
Language:English
Published: MDPI AG 2014-07-01
Series:Chemosensors
Subjects:
SNP
PCR
Online Access:http://www.mdpi.com/2227-9040/2/3/193
id doaj-f295f5005d3f40068560df8c467d126f
record_format Article
spelling doaj-f295f5005d3f40068560df8c467d126f2020-11-24T22:56:00ZengMDPI AGChemosensors2227-90402014-07-012319320610.3390/chemosensors2030193chemosensors2030193Toward Non-Enzymatic Ultrasensitive Identification of Single Nucleotide Polymorphisms by Optical MethodsKira Astakhova0Nucleic Acid Center, Department of Physics, Chemistry and Pharmacy, Campusvej 55, Odense M 5230, DenmarkSingle nucleotide polymorphisms (SNPs) are single nucleotide variations which comprise the most wide spread source of genetic diversity in the genome. Currently, SNPs serve as markers for genetic predispositions, clinically evident disorders and diverse drug responses. Present SNP diagnostics are primarily based on enzymatic reactions in different formats including sequencing, polymerase-chain reaction (PCR) and microarrays. In these assays, the enzymes are applied to address the required sensitivity and specificity when detecting SNP. On the other hand, the development of enzyme-free, simple and robust SNP sensing methods is in a constant focus in research and industry as such assays allow rapid and reproducible SNP diagnostics without the need for expensive equipment and reagents. An ideal method for detection of SNP would entail mixing a DNA or RNA target with a probe to directly obtain a signal. Current assays are still not fulfilling these requirements, although remarkable progress has been achieved in recent years. In this review, current SNP sensing approaches are described with a main focus on recently introduced direct, enzyme-free and ultrasensitive SNP sensing by optical methods.http://www.mdpi.com/2227-9040/2/3/193SNPdiagnosticsPCRenzyme-free assaysfluorescencenanoparticleslocked nucleic acidspolyaromatic hydrocarbons
collection DOAJ
language English
format Article
sources DOAJ
author Kira Astakhova
spellingShingle Kira Astakhova
Toward Non-Enzymatic Ultrasensitive Identification of Single Nucleotide Polymorphisms by Optical Methods
Chemosensors
SNP
diagnostics
PCR
enzyme-free assays
fluorescence
nanoparticles
locked nucleic acids
polyaromatic hydrocarbons
author_facet Kira Astakhova
author_sort Kira Astakhova
title Toward Non-Enzymatic Ultrasensitive Identification of Single Nucleotide Polymorphisms by Optical Methods
title_short Toward Non-Enzymatic Ultrasensitive Identification of Single Nucleotide Polymorphisms by Optical Methods
title_full Toward Non-Enzymatic Ultrasensitive Identification of Single Nucleotide Polymorphisms by Optical Methods
title_fullStr Toward Non-Enzymatic Ultrasensitive Identification of Single Nucleotide Polymorphisms by Optical Methods
title_full_unstemmed Toward Non-Enzymatic Ultrasensitive Identification of Single Nucleotide Polymorphisms by Optical Methods
title_sort toward non-enzymatic ultrasensitive identification of single nucleotide polymorphisms by optical methods
publisher MDPI AG
series Chemosensors
issn 2227-9040
publishDate 2014-07-01
description Single nucleotide polymorphisms (SNPs) are single nucleotide variations which comprise the most wide spread source of genetic diversity in the genome. Currently, SNPs serve as markers for genetic predispositions, clinically evident disorders and diverse drug responses. Present SNP diagnostics are primarily based on enzymatic reactions in different formats including sequencing, polymerase-chain reaction (PCR) and microarrays. In these assays, the enzymes are applied to address the required sensitivity and specificity when detecting SNP. On the other hand, the development of enzyme-free, simple and robust SNP sensing methods is in a constant focus in research and industry as such assays allow rapid and reproducible SNP diagnostics without the need for expensive equipment and reagents. An ideal method for detection of SNP would entail mixing a DNA or RNA target with a probe to directly obtain a signal. Current assays are still not fulfilling these requirements, although remarkable progress has been achieved in recent years. In this review, current SNP sensing approaches are described with a main focus on recently introduced direct, enzyme-free and ultrasensitive SNP sensing by optical methods.
topic SNP
diagnostics
PCR
enzyme-free assays
fluorescence
nanoparticles
locked nucleic acids
polyaromatic hydrocarbons
url http://www.mdpi.com/2227-9040/2/3/193
work_keys_str_mv AT kiraastakhova towardnonenzymaticultrasensitiveidentificationofsinglenucleotidepolymorphismsbyopticalmethods
_version_ 1725655274306404352