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An electrochemical biosensor based on hairpin-DNA aptamer probe and restriction endonuclease for ochratoxin A detection

机译:基于发夹DNA适体探针和限制性核酸内切酶的电化学生物传感器检测曲霉毒素A

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A new electrochemical DNA biosensor based on hairpin anti-ochratoxin A (OTA) aptamer and site-specific DNA cleavage of restriction endonuclease TaqaI was reported in this paper. TaqaI is able to specifically cleave only double strand DNA, but not single strand DNA. The hairpin-DNA aptamer probe (Hap), thiolated single strand DNA labeled with biotin group, was immobilized on a gold electrode. In the presence of OTA, Hap bind with OTA to form Hap-OTA G-quadruplex. Meanwhile, the stem of Hap, which contains a TaqaI recognition site, is opened to form single strand and resistant to the cleavage of TaqaI. After reaction with the streptavidin-HRP, the resulting HRP-tagged Hap-OTA can effectively catalyze the hydrogen peroxide (H_2O_2)-mediated oxidation of 3,3~′,5,5~′-tetramethylbenzidine sulfate (TMB), accompanied by a change from colorless to blue in solution color and an increased electrochemical current signal. However, in the absence of OTA, the biotin group of the Hap can be easily cleaved by TaqaI due to the double-stranded stem, which makes the streptavidin-HRP cannot bind with the Hap and increase electrochemical current signal. By employing the above strategy, this DNA biosensor can detect as low as 0.4 pg/mL OTA with ultrahigh selectivity.
机译:本文报道了一种基于发夹抗-曲霉毒素A(OTA)适体和限制性核酸内切酶TaqaI的位点特异性DNA切割的新型电化学DNA生物传感器。 TaqaI只能特异性切割双链DNA,而不是单链DNA。发夹DNA适体探针(Hap),用生物素基团标记的硫醇化单链DNA,被固定在金电极上。在OTA存在下,Hap与OTA结合形成Hap-OTA G-四链体。同时,包含TaqaI识别位点的Hap茎被打开形成单链,并抵抗TaqaI的裂解。与链霉亲和素-HRP反应后,生成的带有HRP标签的Hap-OTA可以有效催化过氧化氢(H_2O_2)介导的3,3',5,5〜'-硫酸四甲基联苯胺(TMB)的氧化,并伴有溶液颜色从无色变为蓝色,并增加了电化学电流信号。然而,在没有OTA的情况下,由于双链茎,Hap的生物素基团很容易被TaqaI裂解,这使得链霉亲和素-HRP无法与Hap结合并增加电化学电流信号。通过采用上述策略,该DNA生物传感器可以超低选择性检测低至0.4 pg / mL的OTA。

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