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A duplex DNA-gold nanoparticle probe composed as a colorimetric biosensor for sequence-specific DNA-binding proteins
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Ahn, Junho | - |
| dc.contributor.author | Choi, Yeonweon | - |
| dc.contributor.author | Lee, Ae-Ree | - |
| dc.contributor.author | Lee, Joon-Hwa | - |
| dc.contributor.author | Jung, Jong Hwa | - |
| dc.date.accessioned | 2022-12-26T21:24:10Z | - |
| dc.date.available | 2022-12-26T21:24:10Z | - |
| dc.date.issued | 2016 | - |
| dc.identifier.issn | 0003-2654 | - |
| dc.identifier.issn | 1364-5528 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/16845 | - |
| dc.description.abstract | Using duplex DNA-AuNP aggregates, a sequence-specific DNA-binding protein, SQUAMOSA Promoter-binding-Like protein 12 (SPL-12), was directly determined by SPL-12-duplex DNA interaction-based colorimetric actions of DNA-Au assemblies. In order to prepare duplex DNA-Au aggregates, thiol-modified DNA 1 and DNA 2 were attached onto the surface of AuNPs, respectively, by the salt-aging method and then the DNA-attached AuNPs were mixed. Duplex-DNA-Au aggregates having the average size of 160 nm diameter and the maximum absorption at 529 nm were able to recognize SPL-12 and reached the equivalent state by the addition of similar to 30 equivalents of SPL-12 accompanying a color change from red to blue with a red shift of the maximum absorption at 570 nm. As a result, the aggregation size grew to about 247 nm. Also, at higher temperatures of the mixture of duplex-DNA-Au aggregate solution and SPL-12, the equivalent state was reached rapidly. On the contrary, in the control experiment using Bovine Serum Albumin (BSA), no absorption band shift of duplex-DNA-Au aggregates was observed. | - |
| dc.format.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | ROYAL SOC CHEMISTRY | - |
| dc.title | A duplex DNA-gold nanoparticle probe composed as a colorimetric biosensor for sequence-specific DNA-binding proteins | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1039/c6an00033a | - |
| dc.identifier.scopusid | 2-s2.0-84960346528 | - |
| dc.identifier.wosid | 000372259100021 | - |
| dc.identifier.bibliographicCitation | ANALYST, v.141, no.6, pp 2040 - 2045 | - |
| dc.citation.title | ANALYST | - |
| dc.citation.volume | 141 | - |
| dc.citation.number | 6 | - |
| dc.citation.startPage | 2040 | - |
| dc.citation.endPage | 2045 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
| dc.subject.keywordPlus | TRANSCRIPTION FACTORS | - |
| dc.subject.keywordPlus | SBP-DOMAIN | - |
| dc.subject.keywordPlus | FUNCTIONALIZATION | - |
| dc.subject.keywordPlus | GROWTH | - |
| dc.subject.keywordPlus | REPAIR | - |
| dc.subject.keywordPlus | SITE | - |
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