A duplex DNA-gold nanoparticle probe composed as a colorimetric biosensor for sequence-specific DNA-binding proteins

被引:14
作者
Ahn, Junho
Choi, Yeonweon
Lee, Ae-Ree
Lee, Joon-Hwa
Jung, Jong Hwa [1 ]
机构
[1] Gyeongsang Natl Univ, Dept Chem, Jinju 660701, South Korea
关键词
TRANSCRIPTION FACTORS; SBP-DOMAIN; FUNCTIONALIZATION; GROWTH; REPAIR; SITE;
D O I
10.1039/c6an00033a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
收藏
页码:2040 / 2045
页数:6
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