Abstract
A new type of rapid, sensitive, and selective fluorescence turn-on assay was developed for detection of histidine using a DNA–scaffolded silver nanocluster/Cu2+ ensemble (DNA–AgNC/Cu2+). Cu2+ was first bound to nucleic acids of the DNA–AgNCs forming a DNA–AgNC/Cu2+ ensemble and then liberated into solution via the highly specific interaction between histidine and Cu2+ in the presence of other amino acids. The fluorescence of DNA–AgNCs was greatly quenched with the addition of Cu2+, and then the DNA–AgNC/Cu2+ ensemble exhibited marvelous fluorescent enhancement in the presence of histidine, which showed the possibility for constructing a turn-on chemosensor of histidine. Compared to other methods, this approach promises high sensitivity, simplicity in design, convenient operation, and minimized use of organic solvents. The ultra-high selectivity demonstrated the feasibility of the assay for detecting histidine in sophisticated physical environments. The fitting range of the proposed assay is from 0 to 100 μM, with a detection limit of 1.4 μM (S/N = 3) in artificial urine samples. The protocol was evaluated by analysis of artificial urine samples with good recoveries and showed great potential for practical applications.
| Original language | English |
|---|---|
| Pages (from-to) | 3122-3126 |
| Number of pages | 5 |
| Journal | Analyst |
| Volume | 139 |
| Issue number | 12 |
| DOIs | |
| State | Published - 19 Jun 2014 |