Multiplex Fluorescence Melting Curve Analysis for Mutation Detection with Dual-Labeled, Self-Quenched Probes

被引:84
|
作者
Huang, Qiuying [1 ,2 ]
Liu, Zanzan [1 ,2 ]
Liao, Yiqun [3 ]
Chen, Xiaoyun [1 ,2 ]
Zhang, Yi [3 ]
Li, Qingge [1 ,2 ]
机构
[1] Xiamen Univ, Engn Res Ctr Mol Diagnost, Minist Educ, Dept Biomed Sci,Sch Life Sci, Xiamen, Fujian, Peoples R China
[2] Xiamen Univ, Key Lab, Minist Educ Cell Biol & Tumor Cell Engn, Xiamen, Fujian, Peoples R China
[3] Xiamen Univ, Inst Biomed Res, Xiamen, Fujian, Peoples R China
来源
PLOS ONE | 2011年 / 6卷 / 04期
关键词
REAL-TIME PCR; FACTOR-V-LEIDEN; HYBRIDIZATION PROBES; MOLECULAR BEACONS; IDENTIFICATION; SYSTEM; OLIGONUCLEOTIDES; DIAGNOSIS;
D O I
10.1371/journal.pone.0019206
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Probe-based fluorescence melting curve analysis (FMCA) is a powerful tool for mutation detection based on melting temperature generated by thermal denaturation of the probe-target hybrid. Nevertheless, the color multiplexing, probe design, and cross-platform compatibility remain to be limited by using existing probe chemistries. We hereby explored two dual-labeled, self-quenched probes, TaqMan and shared-stem molecular beacons, in their ability to conduct FMCA. Both probes could be directly used for FMCA and readily integrated with closed-tube amplicon hybridization under asymmetric PCR conditions. Improved flexibility of FMCA by using these probes was illustrated in three representative applications of FMCA: mutation scanning, mutation identification and mutation genotyping, all of which achieved improved color-multiplexing with easy probe design and versatile probe combination and all were validated with a large number of real clinical samples. The universal cross-platform compatibility of these probes-based FMCA was also demonstrated by a 4-color mutation genotyping assay performed on five different real-time PCR instruments. The dual-labeled, self-quenched probes offered unprecedented combined advantage of enhanced multiplexing, improved flexibility in probe design, and expanded cross-platform compatibility, which would substantially improve FMCA in mutation detection of various applications.
引用
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页数:9
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