Folding-Upon-Binding and Signal-On Electrochemical DNA Sensor with High Affinity and Specificity

被引:71
作者
Idili, Andrea [1 ]
Amodio, Alessia [1 ,2 ]
Vidonis, Marco [3 ]
Feinberg-Somerson, Jacob [4 ]
Castronovo, Matteo [2 ,3 ,5 ]
Ricci, Francesco [1 ]
机构
[1] Univ Rome, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy
[2] Univ Trieste, Dept Phys, PhD Sch Nanotechnol, I-34127 Trieste, Italy
[3] Univ Udine, Dept Med & Biol Sci & Engn, I-3310 Udine, Italy
[4] Univ Calif Santa Barbara, Program Biomol Sci & Engn, Santa Barbara, CA 93106 USA
[5] CRO Aviano Natl Canc Inst, I-3308 Aviano, Italy
基金
欧洲研究理事会;
关键词
TARGETED TRIPLEX-FORMATION; HYDROGEN-BONDED COMPLEX; ELECTRON-TRANSFER; 1-METHYLTHYMINE; HYBRIDIZATION; REAGENTLESS; VOLTAMMETRY; BIOSENSORS; KINETICS; CLAMPS;
D O I
10.1021/ac501418g
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Here we investigate a novel signal-on electrochemical DNA sensor based on the use of a clamp-like DNA probe that binds a complementary target sequence through two distinct and sequential events, which lead to the formation of a triplex DNA structure. We demonstrate that this target-binding mechanism can improve both the affinity and specificity of recognition as opposed to classic probes solely based on Watson-Crick recognition. By using electrochemical signaling to report the conformational change, we demonstrate a signal-on E-DNA sensor with up to 400% signal gain upon target binding. Moreover, we were able to detect with nanomolar affinity a perfectly matched target as short as 10 bases (K-D = 0.39 nM). Finally, thanks to the molecular double-check provided by the concomitant Watson-Crick and Hoogsteen base pairings involved in target recognition, our sensor provides excellent discrimination efficiency toward a single-base mismatched target.
引用
收藏
页码:9013 / 9019
页数:7
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