Detection of telomerase activity using microchip electrophoresis

被引:6
|
作者
Karasawa, Koji [1 ]
Arakawa, Hidetoshi [1 ]
机构
[1] Showa Univ, Sch Pharm, Dept Analyt Biochem, Shinagawa Ku, Tokyo 1428555, Japan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2015年 / 993卷
关键词
Microchip electrophoresis; Telomerase; Tumor marker; Hydroxypropyl methylcellulose; Polyethylene oxide; Diagnostic assay; REPEAT AMPLIFICATION PROTOCOL; CAPILLARY-ELECTROPHORESIS; GEL-ELECTROPHORESIS; ASSAY; CANCER; RNA; CELLS;
D O I
10.1016/j.jchromb.2015.04.032
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Telomerase participates in malignant transformation or immortalization of cells and thus has attracted attention as an anticancer drug target and diagnostic tumor marker. The telomeric repeat amplification protocol (TRAP) and improved TRAP methods (TRAP-fluorescence, TRAP-hybridization, etc.) are widely used forms of this telomerase assay. However, these approaches generally employ acrylamide gel electrophoresis after amplification of telomeric repeats by polymerase chain reaction (PCR); making these TRAP methods time consuming and technically demanding. In this study we developed a novel telomerase assay using microchip electrophoresis for rapid and highly sensitive detection of telomerase activity in cancer cells. The mixed gel of 0.8% hydroxypropyl methylcellulose (HPMC) and 0.3% polyethylene oxide (PEO) with SYBR Gold (fluorescent reagent) was used for microchip electrophoresis. As a result, the product amplified by a telomerase-positive cell could be measured in one cell per assay and detected with high reproducibility (CV= 0.67%) in the short time of 100 s. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:14 / 19
页数:6
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