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Label-Free Detection of Telomerase Activity in Urine Using Telomerase-Responsive Porous Anodic Alumina Nanochannels

机译:使用端粒酶反应性多孔阳极氧化铝纳米通道对尿液中端粒酶活性进行无标签检测。

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Telomerase is closely related to cancers, which makes it one of the most widely known tumor marker. Recently, many methods have been reported for telomerase activity measurement in which complex label procedures were commonly used. In this paper, a label-free method for detection of telomerase activity in urine based on steric hindrance changes induced by confinement geometry in the porous anodic alumina (PAA) nanochannels was proposed. Telomerase substrate (TS) primer was first assembled on the inside wall of PAA nanochannels by 'Schiff reaction under mild Conditions. Then, under the action of telomerase, TS primer was amplified and extended to repeating Gtrich sequences (TTAGGG)x, which formed multiplex Gquadruplex in the presence of potassium ions (K+). This configurational 'change led to the increment of steric hindrance in the nanochannels, resulting in the decrement of anodic current of potassium ferricyanide (K-3[Fe(CN)(6)]). Compared with previously= reported methods based on PAA nanochannels (usually one G-quadniplek formed), multiplex repeating G-quadruplex formed on one TS primer in this work. As a result, large current drop (similar to 3.6 mu A, 36%) was obtained, Which gave fadlity to improve the detection sensitivity. The decreased ratio of anodic current has a linear correlation with the logarithm of HeLa cell number in the range of 10-5000 cells, with the detection limit of seven cells. The method is simple, reliable, and has, been successfully applied in the detection of telomerase in urine with good accuracy, selectivity and reproducibility. In addition, the method is nondestructive test compared to blood analysis and pathology tests, which is significant for cancer discovery, development, and prognosis.
机译:端粒酶与癌症密切相关,这使其成为最广为人知的肿瘤标志物之一。最近,已经报道了许多用于端粒酶活性测量的方法,其中通常使用复杂的标记方法。本文提出了一种无标记的检测端粒酶活性的方法,该方法基于多孔阳极氧化铝(PAA)纳米通道中的限制几何形状引起的空间位阻变化。端粒酶底物(TS)引物首先通过温和条件下的'席夫(Schiff)反应组装在PAA纳米通道的内壁上。然后,在端粒酶的作用下,将TS引物扩增并延伸至重复的Gtrich序列(TTAGGG)x,在钾离子(K +)存在下形成多重Gquadruplex。这种构型的改变导致纳米通道中空间位阻的增加,导致铁氰化钾(K-3 [Fe(CN)(6)])的阳极电流减少。与以前报道的基于PAA纳米通道(通常形成一个G-四倍体)的方法相比,这项工作中在一个TS引物上形成了多重重复G-四倍体。结果,获得了大的电流降(类似于3.6μA,36%),这为提高检测灵敏度提供了便利。阳极电流比率的降低与HeLa细胞数的对数在10-5000个细胞范围内具有线性关系,检测极限为7个细胞。该方法简便,可靠,已成功应用于尿液中端粒酶的检测,具有较高的准确度,选择性和重现性。此外,与血液分析和病理学检查相比,该方法是非破坏性检查,对于癌症的发现,发展和预后非常重要。

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