A duplex DNA-gold nanoparticle probe composed as a colorimetric biosensor for sequence-specific DNA-binding proteins
- Authors
- Ahn, Junho; Choi, Yeonweon; Lee, Ae-Ree; Lee, Joon-Hwa; Jung, Jong Hwa
- Issue Date
- 2016
- Publisher
- ROYAL SOC CHEMISTRY
- Citation
- ANALYST, v.141, no.6, pp 2040 - 2045
- Pages
- 6
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- ANALYST
- Volume
- 141
- Number
- 6
- Start Page
- 2040
- End Page
- 2045
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/16845
- DOI
- 10.1039/c6an00033a
- ISSN
- 0003-2654
1364-5528
- 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.
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