Loading…
Highly sensitive and selective detection of single-nucleotide polymorphisms using gold nanoparticle MutS enzymes and a micro cantilever resonator
Mutant DNAs are important markers useful for the diagnosis of human disease. Single-nucleotide polymorphisms (SNPs) represent the most common types of DNA mutations. As there is only a one base pair change in a single nucleotide between the SNP and the wild-type DNA, it is difficult to distinguish t...
Saved in:
Published in: | Talanta (Oxford) 2019-12, Vol.205, p.120154-120154, Article 120154 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c431t-36beb3c31face706d503278947a494a2e0c8690180a9fabf505bb145b1d3bd353 |
---|---|
cites | cdi_FETCH-LOGICAL-c431t-36beb3c31face706d503278947a494a2e0c8690180a9fabf505bb145b1d3bd353 |
container_end_page | 120154 |
container_issue | |
container_start_page | 120154 |
container_title | Talanta (Oxford) |
container_volume | 205 |
creator | Park, Chanho Kang, Jimin Baek, Inchul You, Juneseok Jang, Kuewhan Na, Sungsoo |
description | Mutant DNAs are important markers useful for the diagnosis of human disease. Single-nucleotide polymorphisms (SNPs) represent the most common types of DNA mutations. As there is only a one base pair change in a single nucleotide between the SNP and the wild-type DNA, it is difficult to distinguish the SNPs. In this report, a highly sensitive and selective detection and discrimination of SNPs is performed using MutS, gold nanoparticles (AuNP) and a resonator. A single mismatched base exists between the SNP mutation and the probe DNA on the resonator, and MutS binds to the DNA at the location of the mismatch. As MutS is attached to AuNP (MutS-AuNP), both MutS and AuNP are adsorbed onto the resonator. The detection is based on the resonance frequency shift of the resonator following the adsorption of MutS-AuNP on the resonator. Highly sensitive detection of DNA mutations was achieved using AuNPs that act as mass amplifiers, and the obtained limit of detected was 100 fM. Additionally, our proposed method detected mutations in the presence of as little as 0.1% wild-type, and discrimination of specific mutations was also achieved. The results obtained from our proposed method suggest its potential for diagnosing cancer patients.
[Display omitted]
•Single-nucleotide polymorphisms (SNPs) are detected using mismatch recognition protein and micro resonator.•The detection is based on the resonance frequency shift of micro resonator.•High sensitive detection of SNPs (limit of detection: 100fM) is achieved by introducing gold nanoparticle.•Mutatant DNA is detected in the presence of wild-type, as little as 0.1%.•Discrimination of specific SNP mutation is also performed..•Our proposed method has shown potential glimpses of a personalized medical diagnosis for cancer patients. |
doi_str_mv | 10.1016/j.talanta.2019.120154 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2281102807</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0039914019307805</els_id><sourcerecordid>2281102807</sourcerecordid><originalsourceid>FETCH-LOGICAL-c431t-36beb3c31face706d503278947a494a2e0c8690180a9fabf505bb145b1d3bd353</originalsourceid><addsrcrecordid>eNqFkcFu1DAQhi1ERZfCI4B85JJlHDub5IRQVShSqx4KZ8uxJ1uvHDvYzkrLW_DGeLsLVy62R_pmxv__E_KOwZoB23zcrbNyyme1roH1a1bORrwgK9a1vOJNy1-SFQDvq54JuCSvU9oBQM2BvyKXnIkGhKhX5Pet3T65A03ok812j1R5UyqH-rkymI-v4GkYabJ-67Dyi3YYsjVI5-AOU4jzk01TossRoNvgDPXKh1nFbAtK75f8SNH_OkyYnucrOlkdA9VFgHW4x0gjpuBVDvENuRiVS_j2fF-RH19uvl_fVncPX79df76rtOAsV3wz4MA1Z6PS2MLGNMDrtutFq0QvVI2gu00PrAPVj2oYG2iGocgemOGD4Q2_Ih9Oc-cYfi6Yspxs0uiKqRiWJOu6YwzqDtqCNie0_DmliKOco51UPEgG8piG3MlzGvKYhjylUfren1csw4TmX9df-wvw6QRgEbq3GGXSFr1GY2OxXZpg_7PiD3jsoaA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2281102807</pqid></control><display><type>article</type><title>Highly sensitive and selective detection of single-nucleotide polymorphisms using gold nanoparticle MutS enzymes and a micro cantilever resonator</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Park, Chanho ; Kang, Jimin ; Baek, Inchul ; You, Juneseok ; Jang, Kuewhan ; Na, Sungsoo</creator><creatorcontrib>Park, Chanho ; Kang, Jimin ; Baek, Inchul ; You, Juneseok ; Jang, Kuewhan ; Na, Sungsoo</creatorcontrib><description>Mutant DNAs are important markers useful for the diagnosis of human disease. Single-nucleotide polymorphisms (SNPs) represent the most common types of DNA mutations. As there is only a one base pair change in a single nucleotide between the SNP and the wild-type DNA, it is difficult to distinguish the SNPs. In this report, a highly sensitive and selective detection and discrimination of SNPs is performed using MutS, gold nanoparticles (AuNP) and a resonator. A single mismatched base exists between the SNP mutation and the probe DNA on the resonator, and MutS binds to the DNA at the location of the mismatch. As MutS is attached to AuNP (MutS-AuNP), both MutS and AuNP are adsorbed onto the resonator. The detection is based on the resonance frequency shift of the resonator following the adsorption of MutS-AuNP on the resonator. Highly sensitive detection of DNA mutations was achieved using AuNPs that act as mass amplifiers, and the obtained limit of detected was 100 fM. Additionally, our proposed method detected mutations in the presence of as little as 0.1% wild-type, and discrimination of specific mutations was also achieved. The results obtained from our proposed method suggest its potential for diagnosing cancer patients.
[Display omitted]
•Single-nucleotide polymorphisms (SNPs) are detected using mismatch recognition protein and micro resonator.•The detection is based on the resonance frequency shift of micro resonator.•High sensitive detection of SNPs (limit of detection: 100fM) is achieved by introducing gold nanoparticle.•Mutatant DNA is detected in the presence of wild-type, as little as 0.1%.•Discrimination of specific SNP mutation is also performed..•Our proposed method has shown potential glimpses of a personalized medical diagnosis for cancer patients.</description><identifier>ISSN: 0039-9140</identifier><identifier>EISSN: 1873-3573</identifier><identifier>DOI: 10.1016/j.talanta.2019.120154</identifier><identifier>PMID: 31450442</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>DNA detection ; Gold - chemistry ; Gold nanoparticle (AuNP) ; Humans ; Kirsten rat sarcoma viral oncogene homolog (KRAS) ; Limit of Detection ; Metal Nanoparticles - chemistry ; Microtechnology - instrumentation ; Molecular Dynamics Simulation ; Mutant DNA ; Mutation ; MutS DNA Mismatch-Binding Protein - chemistry ; MutS DNA Mismatch-Binding Protein - metabolism ; Particle Size ; Polymorphism, Single Nucleotide ; Protein Conformation ; Proto-Oncogene Proteins p21(ras) - genetics ; Resonance frequency shift ; Single nucleotide polymorphism</subject><ispartof>Talanta (Oxford), 2019-12, Vol.205, p.120154-120154, Article 120154</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-36beb3c31face706d503278947a494a2e0c8690180a9fabf505bb145b1d3bd353</citedby><cites>FETCH-LOGICAL-c431t-36beb3c31face706d503278947a494a2e0c8690180a9fabf505bb145b1d3bd353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31450442$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Chanho</creatorcontrib><creatorcontrib>Kang, Jimin</creatorcontrib><creatorcontrib>Baek, Inchul</creatorcontrib><creatorcontrib>You, Juneseok</creatorcontrib><creatorcontrib>Jang, Kuewhan</creatorcontrib><creatorcontrib>Na, Sungsoo</creatorcontrib><title>Highly sensitive and selective detection of single-nucleotide polymorphisms using gold nanoparticle MutS enzymes and a micro cantilever resonator</title><title>Talanta (Oxford)</title><addtitle>Talanta</addtitle><description>Mutant DNAs are important markers useful for the diagnosis of human disease. Single-nucleotide polymorphisms (SNPs) represent the most common types of DNA mutations. As there is only a one base pair change in a single nucleotide between the SNP and the wild-type DNA, it is difficult to distinguish the SNPs. In this report, a highly sensitive and selective detection and discrimination of SNPs is performed using MutS, gold nanoparticles (AuNP) and a resonator. A single mismatched base exists between the SNP mutation and the probe DNA on the resonator, and MutS binds to the DNA at the location of the mismatch. As MutS is attached to AuNP (MutS-AuNP), both MutS and AuNP are adsorbed onto the resonator. The detection is based on the resonance frequency shift of the resonator following the adsorption of MutS-AuNP on the resonator. Highly sensitive detection of DNA mutations was achieved using AuNPs that act as mass amplifiers, and the obtained limit of detected was 100 fM. Additionally, our proposed method detected mutations in the presence of as little as 0.1% wild-type, and discrimination of specific mutations was also achieved. The results obtained from our proposed method suggest its potential for diagnosing cancer patients.
[Display omitted]
•Single-nucleotide polymorphisms (SNPs) are detected using mismatch recognition protein and micro resonator.•The detection is based on the resonance frequency shift of micro resonator.•High sensitive detection of SNPs (limit of detection: 100fM) is achieved by introducing gold nanoparticle.•Mutatant DNA is detected in the presence of wild-type, as little as 0.1%.•Discrimination of specific SNP mutation is also performed..•Our proposed method has shown potential glimpses of a personalized medical diagnosis for cancer patients.</description><subject>DNA detection</subject><subject>Gold - chemistry</subject><subject>Gold nanoparticle (AuNP)</subject><subject>Humans</subject><subject>Kirsten rat sarcoma viral oncogene homolog (KRAS)</subject><subject>Limit of Detection</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Microtechnology - instrumentation</subject><subject>Molecular Dynamics Simulation</subject><subject>Mutant DNA</subject><subject>Mutation</subject><subject>MutS DNA Mismatch-Binding Protein - chemistry</subject><subject>MutS DNA Mismatch-Binding Protein - metabolism</subject><subject>Particle Size</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Protein Conformation</subject><subject>Proto-Oncogene Proteins p21(ras) - genetics</subject><subject>Resonance frequency shift</subject><subject>Single nucleotide polymorphism</subject><issn>0039-9140</issn><issn>1873-3573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhi1ERZfCI4B85JJlHDub5IRQVShSqx4KZ8uxJ1uvHDvYzkrLW_DGeLsLVy62R_pmxv__E_KOwZoB23zcrbNyyme1roH1a1bORrwgK9a1vOJNy1-SFQDvq54JuCSvU9oBQM2BvyKXnIkGhKhX5Pet3T65A03ok812j1R5UyqH-rkymI-v4GkYabJ-67Dyi3YYsjVI5-AOU4jzk01TossRoNvgDPXKh1nFbAtK75f8SNH_OkyYnucrOlkdA9VFgHW4x0gjpuBVDvENuRiVS_j2fF-RH19uvl_fVncPX79df76rtOAsV3wz4MA1Z6PS2MLGNMDrtutFq0QvVI2gu00PrAPVj2oYG2iGocgemOGD4Q2_Ih9Oc-cYfi6Yspxs0uiKqRiWJOu6YwzqDtqCNie0_DmliKOco51UPEgG8piG3MlzGvKYhjylUfren1csw4TmX9df-wvw6QRgEbq3GGXSFr1GY2OxXZpg_7PiD3jsoaA</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Park, Chanho</creator><creator>Kang, Jimin</creator><creator>Baek, Inchul</creator><creator>You, Juneseok</creator><creator>Jang, Kuewhan</creator><creator>Na, Sungsoo</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20191201</creationdate><title>Highly sensitive and selective detection of single-nucleotide polymorphisms using gold nanoparticle MutS enzymes and a micro cantilever resonator</title><author>Park, Chanho ; Kang, Jimin ; Baek, Inchul ; You, Juneseok ; Jang, Kuewhan ; Na, Sungsoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-36beb3c31face706d503278947a494a2e0c8690180a9fabf505bb145b1d3bd353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>DNA detection</topic><topic>Gold - chemistry</topic><topic>Gold nanoparticle (AuNP)</topic><topic>Humans</topic><topic>Kirsten rat sarcoma viral oncogene homolog (KRAS)</topic><topic>Limit of Detection</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Microtechnology - instrumentation</topic><topic>Molecular Dynamics Simulation</topic><topic>Mutant DNA</topic><topic>Mutation</topic><topic>MutS DNA Mismatch-Binding Protein - chemistry</topic><topic>MutS DNA Mismatch-Binding Protein - metabolism</topic><topic>Particle Size</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Protein Conformation</topic><topic>Proto-Oncogene Proteins p21(ras) - genetics</topic><topic>Resonance frequency shift</topic><topic>Single nucleotide polymorphism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Chanho</creatorcontrib><creatorcontrib>Kang, Jimin</creatorcontrib><creatorcontrib>Baek, Inchul</creatorcontrib><creatorcontrib>You, Juneseok</creatorcontrib><creatorcontrib>Jang, Kuewhan</creatorcontrib><creatorcontrib>Na, Sungsoo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Talanta (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Chanho</au><au>Kang, Jimin</au><au>Baek, Inchul</au><au>You, Juneseok</au><au>Jang, Kuewhan</au><au>Na, Sungsoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Highly sensitive and selective detection of single-nucleotide polymorphisms using gold nanoparticle MutS enzymes and a micro cantilever resonator</atitle><jtitle>Talanta (Oxford)</jtitle><addtitle>Talanta</addtitle><date>2019-12-01</date><risdate>2019</risdate><volume>205</volume><spage>120154</spage><epage>120154</epage><pages>120154-120154</pages><artnum>120154</artnum><issn>0039-9140</issn><eissn>1873-3573</eissn><abstract>Mutant DNAs are important markers useful for the diagnosis of human disease. Single-nucleotide polymorphisms (SNPs) represent the most common types of DNA mutations. As there is only a one base pair change in a single nucleotide between the SNP and the wild-type DNA, it is difficult to distinguish the SNPs. In this report, a highly sensitive and selective detection and discrimination of SNPs is performed using MutS, gold nanoparticles (AuNP) and a resonator. A single mismatched base exists between the SNP mutation and the probe DNA on the resonator, and MutS binds to the DNA at the location of the mismatch. As MutS is attached to AuNP (MutS-AuNP), both MutS and AuNP are adsorbed onto the resonator. The detection is based on the resonance frequency shift of the resonator following the adsorption of MutS-AuNP on the resonator. Highly sensitive detection of DNA mutations was achieved using AuNPs that act as mass amplifiers, and the obtained limit of detected was 100 fM. Additionally, our proposed method detected mutations in the presence of as little as 0.1% wild-type, and discrimination of specific mutations was also achieved. The results obtained from our proposed method suggest its potential for diagnosing cancer patients.
[Display omitted]
•Single-nucleotide polymorphisms (SNPs) are detected using mismatch recognition protein and micro resonator.•The detection is based on the resonance frequency shift of micro resonator.•High sensitive detection of SNPs (limit of detection: 100fM) is achieved by introducing gold nanoparticle.•Mutatant DNA is detected in the presence of wild-type, as little as 0.1%.•Discrimination of specific SNP mutation is also performed..•Our proposed method has shown potential glimpses of a personalized medical diagnosis for cancer patients.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31450442</pmid><doi>10.1016/j.talanta.2019.120154</doi><tpages>1</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0039-9140 |
ispartof | Talanta (Oxford), 2019-12, Vol.205, p.120154-120154, Article 120154 |
issn | 0039-9140 1873-3573 |
language | eng |
recordid | cdi_proquest_miscellaneous_2281102807 |
source | ScienceDirect Freedom Collection 2022-2024 |
subjects | DNA detection Gold - chemistry Gold nanoparticle (AuNP) Humans Kirsten rat sarcoma viral oncogene homolog (KRAS) Limit of Detection Metal Nanoparticles - chemistry Microtechnology - instrumentation Molecular Dynamics Simulation Mutant DNA Mutation MutS DNA Mismatch-Binding Protein - chemistry MutS DNA Mismatch-Binding Protein - metabolism Particle Size Polymorphism, Single Nucleotide Protein Conformation Proto-Oncogene Proteins p21(ras) - genetics Resonance frequency shift Single nucleotide polymorphism |
title | Highly sensitive and selective detection of single-nucleotide polymorphisms using gold nanoparticle MutS enzymes and a micro cantilever resonator |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T06%3A18%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Highly%20sensitive%20and%20selective%20detection%20of%20single-nucleotide%20polymorphisms%20using%20gold%20nanoparticle%20MutS%20enzymes%20and%20a%20micro%20cantilever%20resonator&rft.jtitle=Talanta%20(Oxford)&rft.au=Park,%20Chanho&rft.date=2019-12-01&rft.volume=205&rft.spage=120154&rft.epage=120154&rft.pages=120154-120154&rft.artnum=120154&rft.issn=0039-9140&rft.eissn=1873-3573&rft_id=info:doi/10.1016/j.talanta.2019.120154&rft_dat=%3Cproquest_cross%3E2281102807%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c431t-36beb3c31face706d503278947a494a2e0c8690180a9fabf505bb145b1d3bd353%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2281102807&rft_id=info:pmid/31450442&rfr_iscdi=true |