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Methylene Blue as a G‑Quadruplex Binding Probe for Label-Free Homogeneous Electrochemical Biosensing
Herein, G-quadruplex sequence was found to significantly decrease the diffusion current of methylene blue (MB) in homogeneous solution for the first time. Electrochemical methods combined with circular dichroism spectroscopy and UV–vis spectroscopy were utilized to systematically explore the interac...
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Published in: | Analytical chemistry (Washington) 2014-10, Vol.86 (19), p.9489-9495 |
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description | Herein, G-quadruplex sequence was found to significantly decrease the diffusion current of methylene blue (MB) in homogeneous solution for the first time. Electrochemical methods combined with circular dichroism spectroscopy and UV–vis spectroscopy were utilized to systematically explore the interaction between MB and an artificial G-quadruplex sequence, EAD2. The interaction of MB and EAD2 (the binding constant, K ≈ 1.3 × 106 M–1) was stronger than that of MB and double-stranded DNA (dsDNA) (K ≈ 2.2 × 105 M–1), and the binding stoichiometry (n) of EAD2/MB complex was calculated to be 1.0 according to the electrochemical titration curve combined with Scatchard analysis. MB was proved to stabilize the G-quadruplex structure of EAD2 and showed a competitive binding to G-quadruplex in the presence of hemin. EAD2 might mainly interact with MB, a positive ligand of G-quadruplex, through the end-stacking with π-system of the guanine quartet, which was quite different from the binding mechanism of dsDNA with MB by intercalation. A novel signal read-out mode based on the strong affinity between G-quadruplex and MB coupling with aptamer/G-quadruplex hairpin structure was successfully implemented in cocaine detection with high specificity. G-quadruplex/MB complex will function as a promising electrochemical indicator for constructing homogeneous label-free electrochemical biosensors, especially in the field of simple, rapid, and noninvasive biochemical assays. |
doi_str_mv | 10.1021/ac502540m |
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Electrochemical methods combined with circular dichroism spectroscopy and UV–vis spectroscopy were utilized to systematically explore the interaction between MB and an artificial G-quadruplex sequence, EAD2. The interaction of MB and EAD2 (the binding constant, K ≈ 1.3 × 106 M–1) was stronger than that of MB and double-stranded DNA (dsDNA) (K ≈ 2.2 × 105 M–1), and the binding stoichiometry (n) of EAD2/MB complex was calculated to be 1.0 according to the electrochemical titration curve combined with Scatchard analysis. MB was proved to stabilize the G-quadruplex structure of EAD2 and showed a competitive binding to G-quadruplex in the presence of hemin. EAD2 might mainly interact with MB, a positive ligand of G-quadruplex, through the end-stacking with π-system of the guanine quartet, which was quite different from the binding mechanism of dsDNA with MB by intercalation. A novel signal read-out mode based on the strong affinity between G-quadruplex and MB coupling with aptamer/G-quadruplex hairpin structure was successfully implemented in cocaine detection with high specificity. G-quadruplex/MB complex will function as a promising electrochemical indicator for constructing homogeneous label-free electrochemical biosensors, especially in the field of simple, rapid, and noninvasive biochemical assays.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/ac502540m</identifier><identifier>PMID: 25211349</identifier><identifier>CODEN: ANCHAM</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Analytical chemistry ; Aptamers, Nucleotide - chemistry ; Binding ; Binding, Competitive ; Bioassays ; Biochemistry ; Biosensing Techniques ; Biosensors ; Chemical compounds ; Cocaine - isolation & purification ; Constants ; Deoxyribonucleic acid ; Dichroism ; DNA ; DNA - chemistry ; Electrochemical Techniques ; G-Quadruplexes ; Hemin - chemistry ; Methylene blue ; Methylene Blue - chemistry ; Solutions ; Spectroscopy ; Spectrum analysis ; Symbols</subject><ispartof>Analytical chemistry (Washington), 2014-10, Vol.86 (19), p.9489-9495</ispartof><rights>Copyright American Chemical Society Oct 7, 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a409t-9a9f11267d95b42c6039d530e1cbbd89f6c9a1d4b48e798343b7986f19c2bbd23</citedby><cites>FETCH-LOGICAL-a409t-9a9f11267d95b42c6039d530e1cbbd89f6c9a1d4b48e798343b7986f19c2bbd23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25211349$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Fang-Ting</creatorcontrib><creatorcontrib>Nie, Ji</creatorcontrib><creatorcontrib>Zhang, De-Wen</creatorcontrib><creatorcontrib>Chen, Ji-Tao</creatorcontrib><creatorcontrib>Zhou, Ying-Lin</creatorcontrib><creatorcontrib>Zhang, Xin-Xiang</creatorcontrib><title>Methylene Blue as a G‑Quadruplex Binding Probe for Label-Free Homogeneous Electrochemical Biosensing</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>Herein, G-quadruplex sequence was found to significantly decrease the diffusion current of methylene blue (MB) in homogeneous solution for the first time. Electrochemical methods combined with circular dichroism spectroscopy and UV–vis spectroscopy were utilized to systematically explore the interaction between MB and an artificial G-quadruplex sequence, EAD2. The interaction of MB and EAD2 (the binding constant, K ≈ 1.3 × 106 M–1) was stronger than that of MB and double-stranded DNA (dsDNA) (K ≈ 2.2 × 105 M–1), and the binding stoichiometry (n) of EAD2/MB complex was calculated to be 1.0 according to the electrochemical titration curve combined with Scatchard analysis. MB was proved to stabilize the G-quadruplex structure of EAD2 and showed a competitive binding to G-quadruplex in the presence of hemin. EAD2 might mainly interact with MB, a positive ligand of G-quadruplex, through the end-stacking with π-system of the guanine quartet, which was quite different from the binding mechanism of dsDNA with MB by intercalation. A novel signal read-out mode based on the strong affinity between G-quadruplex and MB coupling with aptamer/G-quadruplex hairpin structure was successfully implemented in cocaine detection with high specificity. G-quadruplex/MB complex will function as a promising electrochemical indicator for constructing homogeneous label-free electrochemical biosensors, especially in the field of simple, rapid, and noninvasive biochemical assays.</description><subject>Analytical chemistry</subject><subject>Aptamers, Nucleotide - chemistry</subject><subject>Binding</subject><subject>Binding, Competitive</subject><subject>Bioassays</subject><subject>Biochemistry</subject><subject>Biosensing Techniques</subject><subject>Biosensors</subject><subject>Chemical compounds</subject><subject>Cocaine - isolation & purification</subject><subject>Constants</subject><subject>Deoxyribonucleic acid</subject><subject>Dichroism</subject><subject>DNA</subject><subject>DNA - chemistry</subject><subject>Electrochemical Techniques</subject><subject>G-Quadruplexes</subject><subject>Hemin - chemistry</subject><subject>Methylene blue</subject><subject>Methylene Blue - chemistry</subject><subject>Solutions</subject><subject>Spectroscopy</subject><subject>Spectrum analysis</subject><subject>Symbols</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqN0ctO3TAQBmALUcHhsuAFKkuoEiwCM3acxEtAXCqdCpDadeQ4Ewhy4lP7RCq7vkJfkSfB9FBUtRtWs_nm91g_Y3sIRwgCj41VIFQOwxqboRKQFVUl1tkMAGQmSoBNthXjAwAiYLHBNoUSiDLXM9Z9oeX9o6OR-KmbiJvIDb98-vnrdjJtmBaOfvDTfmz78Y7fBN8Q73zgc9OQyy4CEb_yg79L636K_NyRXQZv72norXFp0UcaY9rdYR864yLtvs5t9u3i_OvZVTa_vvx8djLPTA56mWmjO0RRlK1WTS5sAVK3SgKhbZq20l1htcE2b_KKSl3JXDZpFB1qKxIQcpsdrHIXwX-fKC7roY-WnDO_L6yx0EIqLMv3UCEKUJWU76CgJaRzdKL7_9AHP4Ux_TkpzCsQoMqkDlfKBh9joK5ehH4w4bFGqF8qrd8qTfbja-LUDNS-yT8dJvBpBYyNf732X9AzM9amBA</recordid><startdate>20141007</startdate><enddate>20141007</enddate><creator>Zhang, Fang-Ting</creator><creator>Nie, Ji</creator><creator>Zhang, De-Wen</creator><creator>Chen, Ji-Tao</creator><creator>Zhou, Ying-Lin</creator><creator>Zhang, Xin-Xiang</creator><general>American Chemical Society</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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20141007</creationdate><title>Methylene Blue as a G‑Quadruplex Binding Probe for Label-Free Homogeneous Electrochemical Biosensing</title><author>Zhang, Fang-Ting ; Nie, Ji ; Zhang, De-Wen ; Chen, Ji-Tao ; Zhou, Ying-Lin ; Zhang, Xin-Xiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a409t-9a9f11267d95b42c6039d530e1cbbd89f6c9a1d4b48e798343b7986f19c2bbd23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Analytical chemistry</topic><topic>Aptamers, Nucleotide - chemistry</topic><topic>Binding</topic><topic>Binding, Competitive</topic><topic>Bioassays</topic><topic>Biochemistry</topic><topic>Biosensing Techniques</topic><topic>Biosensors</topic><topic>Chemical compounds</topic><topic>Cocaine - isolation & purification</topic><topic>Constants</topic><topic>Deoxyribonucleic acid</topic><topic>Dichroism</topic><topic>DNA</topic><topic>DNA - chemistry</topic><topic>Electrochemical Techniques</topic><topic>G-Quadruplexes</topic><topic>Hemin - chemistry</topic><topic>Methylene blue</topic><topic>Methylene Blue - chemistry</topic><topic>Solutions</topic><topic>Spectroscopy</topic><topic>Spectrum analysis</topic><topic>Symbols</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Fang-Ting</creatorcontrib><creatorcontrib>Nie, Ji</creatorcontrib><creatorcontrib>Zhang, De-Wen</creatorcontrib><creatorcontrib>Chen, Ji-Tao</creatorcontrib><creatorcontrib>Zhou, Ying-Lin</creatorcontrib><creatorcontrib>Zhang, Xin-Xiang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Fang-Ting</au><au>Nie, Ji</au><au>Zhang, De-Wen</au><au>Chen, Ji-Tao</au><au>Zhou, Ying-Lin</au><au>Zhang, Xin-Xiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methylene Blue as a G‑Quadruplex Binding Probe for Label-Free Homogeneous Electrochemical Biosensing</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2014-10-07</date><risdate>2014</risdate><volume>86</volume><issue>19</issue><spage>9489</spage><epage>9495</epage><pages>9489-9495</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><coden>ANCHAM</coden><abstract>Herein, G-quadruplex sequence was found to significantly decrease the diffusion current of methylene blue (MB) in homogeneous solution for the first time. Electrochemical methods combined with circular dichroism spectroscopy and UV–vis spectroscopy were utilized to systematically explore the interaction between MB and an artificial G-quadruplex sequence, EAD2. The interaction of MB and EAD2 (the binding constant, K ≈ 1.3 × 106 M–1) was stronger than that of MB and double-stranded DNA (dsDNA) (K ≈ 2.2 × 105 M–1), and the binding stoichiometry (n) of EAD2/MB complex was calculated to be 1.0 according to the electrochemical titration curve combined with Scatchard analysis. MB was proved to stabilize the G-quadruplex structure of EAD2 and showed a competitive binding to G-quadruplex in the presence of hemin. EAD2 might mainly interact with MB, a positive ligand of G-quadruplex, through the end-stacking with π-system of the guanine quartet, which was quite different from the binding mechanism of dsDNA with MB by intercalation. A novel signal read-out mode based on the strong affinity between G-quadruplex and MB coupling with aptamer/G-quadruplex hairpin structure was successfully implemented in cocaine detection with high specificity. G-quadruplex/MB complex will function as a promising electrochemical indicator for constructing homogeneous label-free electrochemical biosensors, especially in the field of simple, rapid, and noninvasive biochemical assays.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>25211349</pmid><doi>10.1021/ac502540m</doi><tpages>7</tpages></addata></record> |
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subjects | Analytical chemistry Aptamers, Nucleotide - chemistry Binding Binding, Competitive Bioassays Biochemistry Biosensing Techniques Biosensors Chemical compounds Cocaine - isolation & purification Constants Deoxyribonucleic acid Dichroism DNA DNA - chemistry Electrochemical Techniques G-Quadruplexes Hemin - chemistry Methylene blue Methylene Blue - chemistry Solutions Spectroscopy Spectrum analysis Symbols |
title | Methylene Blue as a G‑Quadruplex Binding Probe for Label-Free Homogeneous Electrochemical Biosensing |
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