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Biosensor Techniques Used for Determination of Telomerase Activity in Cancer Cells

机译:用于确定癌细胞端粒酶活性的生物传感器技术

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摘要

Measuring telomerase activity has proven successful for the determination of cancer in malignant somatic cells. Early conventional methods for the detection of telomerase activity include in vitro analysis via a primer extension assay, and the telomeric repeat amplification protocol (TRAP) assay. TRAP incorporates the polymerase chain reaction (PCR) step to increase the sensitivity of a given sample. However, research suggests that the TRAP technique suffers from false negative results, caused by failure of its PCR step. Other limitations of TRAP include the post-PCR steps involving polyacrylamide gel electrophoresis which are time inefficient. Thus, various efforts have been made to eliminate the PCR step of TRAP by using a variety of biosensor detection devices. This review mainly focuses on these alternatives including: optical, electrochemical, magnetic, and nanowire conductive signaling techniques to measure the telomerase activity produced via label free biosensor assay—via biocatalytic labels involving beacons, DNAzyme, ferrocenyl-naphthalene diimides, avidin-alkaline phosphatase and semiconductor quantum dots (QDs). These biosensor techniques are sensitive and provide precise and rapid results in the detection of telomerase activity.
机译:端粒酶活性的测定已被证明可以成功地测定恶性体细胞中的癌症。早期检测端粒酶活性的常规方法包括通过引物延伸分析和端粒重复扩增协议(TRAP)分析的体外分析。 TRAP引入了聚合酶链反应(PCR)步骤,以增加给定样品的灵敏度。然而,研究表明,TRAP技术由于其PCR步骤失败而遭受假阴性结果的困扰。 TRAP的其他局限性包括PCR反应后步骤,该步骤涉及时间效率低的聚丙烯酰胺凝胶电泳。因此,已经进行了各种努力以通过使用各种生物传感器检测装置来消除TRAP的PCR步骤。这篇综述主要侧重于这些替代方案,包括:光学,电化学,磁性和纳米线导电信号传导技术,用于测量通过无标记生物传感器测定产生的端粒酶活性-通过涉及信标,DNAzyme,二茂铁基萘二酰亚胺,抗生物素蛋白碱性磷酸酶和半导体量子点(QD)。这些生物传感器技术灵敏,可在端粒酶活性检测中提供准确而快速的结果。

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