Sub-7-second genotyping of single-nucleotide polymorphism by high-resolution melting curve analysis on a thermal digital microfluidic device

被引:26
|
作者
Chen, Tianlan [1 ,2 ]
Jia, Yanwei [1 ]
Dong, Cheng [1 ,2 ]
Gao, Jie [1 ,2 ]
Mak, Pui-In [1 ,2 ]
Martins, Rui P. [1 ,2 ]
机构
[1] Univ Macau, State Key Lab Analog & Mixed Signal VLSI, Macau, Peoples R China
[2] Univ Macau, Fac Sci & Technol ECE, Macau, Peoples R China
关键词
POLYMERASE-CHAIN-REACTION; CAPILLARY-ELECTROPHORESIS; PCR AMPLIFICATION; DNA MICROARRAY; CHIP; MUTATION; SYSTEM; PLATFORM; GENOME; HYBRIDIZATION;
D O I
10.1039/c5lc01533b
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We developed a thermal digital microfluidic (T-DMF) device enabling ultrafast DNA melting curve analysis (MCA). Within 7 seconds, the T-DMF device succeeded in differentiating a melting point difference down to 1.6 degrees C with a variation of 0.3 degrees C in a tiny droplet sample (1.2 mu L), which was 300 times faster and with 20 times less sample spending than the standard MCA (35 minutes, 25 mu L) run in a commercial qPCR machine. Such a performance makes it possible for a rapid discrimination of single-nucleotide mutation relevant to prompt clinical decision-making. Also, aided by electronic intelligent control, the T-DMF device facilitates sample handling and pipelining in an automatic serial manner. An optimized oval-shaped thermal electrode is introduced to achieve high thermal uniformity. A device-sealing technique averts sample contamination and permits uninterrupted chemical/biological reactions. Simple fabrication using a single chromium layer fulfills both the thermal and typical transport electrode requirements. Capable of thermally modulating DNA samples with ultrafast MCA, this T-DMF device has the potential for a wide variety of life science analyses, especially for disease diagnosis and prognosis.
引用
收藏
页码:743 / 752
页数:10
相关论文
共 50 条
  • [41] High-resolution melting analysis for genotyping of the myotonic dystrophy type 1 associated Alu insertion/deletion polymorphism
    Radvansky, Jan
    Resko, Peter
    Surovy, Milan
    Minarik, Gabriel
    Ficek, Andrej
    Kadasi, Ludevit
    ANALYTICAL BIOCHEMISTRY, 2010, 398 (01) : 126 - 128
  • [42] The high-resolution genomic profiling using wholegenome single nucleotide polymorphism genotyping in clear cell renal cell carcinoma
    Yokomizo, Akira
    Yamamoto, Ken
    Tada, Yasuhiro
    Naito, Seiji
    JOURNAL OF UROLOGY, 2008, 179 (04): : 93 - 93
  • [43] High-resolution melting (HRM) analysis for the detection of single nucleotide polymorphisms in microRNA target sites
    Lin, Pei-Chin
    Liu, Ta-Chih
    Chang, Chun-Chi
    Chen, Yung-Hsiu
    Chang, Jan-Gowth
    CLINICA CHIMICA ACTA, 2012, 413 (13-14) : 1092 - 1097
  • [44] Rapid Identification of Echinococcus granulosus and E-canadensis Using High-Resolution Melting (HRM) Analysis by Focusing on a Single Nucleotide Polymorphism
    Safa, Ahmad Hosseini
    Harandi, Majid Fasihi
    Tajaddini, Mohammadhasan
    Rostami-Nejad, Mohammad
    Mohtashami-Pour, Mehdi
    Pestehchian, Nader
    JAPANESE JOURNAL OF INFECTIOUS DISEASES, 2016, 69 (04) : 300 - 305
  • [45] GENETIC ANALYSIS OF PEDIATRIC BRAIN STEM GLIOMAS BY HIGH-RESOLUTION SINGLE-NUCLEOTIDE POLYMORPHISM ARRAYS USING WHOLE-GENOME AMPLIFIED DNA
    Lee, Eric
    Monsalvcs, Eric
    Solomon, Lauren
    Bartels, Ute
    Hawkins, Cynthia
    NEURO-ONCOLOGY, 2008, 10 (05) : 801 - 802
  • [46] High-resolution melting curve analysis for genotyping of common SNP in MTHFR gene using fixed-cell suspension
    Sinthuwiwat, Thivaratana
    Poowasanpetch, Phanasit
    Wongngamrungroj, Angsana
    Promso, Somying
    Auewarakul, Chirayu
    Mooney, Sean
    Tocharoentanaphol, Chintana
    MOLECULAR AND CELLULAR PROBES, 2008, 22 (5-6) : 329 - 332
  • [47] High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays
    Carr, Jane
    Bown, Nick P.
    Case, Marian C.
    Hall, Andrew G.
    Lunec, John
    Tweddle, Deborah A.
    CANCER GENETICS AND CYTOGENETICS, 2007, 172 (02) : 127 - 138
  • [48] Identification of TCTE3 as a gene responsible for congenital diaphragmatic hernia using a high-resolution single-nucleotide polymorphism array
    Risa Teshiba
    Kouji Masumoto
    Genshiro Esumi
    Kouji Nagata
    Yoshiaki Kinoshita
    Tatsuro Tajiri
    Tomoaki Taguchi
    Ken Yamamoto
    Pediatric Surgery International, 2011, 27 : 193 - 198
  • [49] Identification of TCTE3 as a gene responsible for congenital diaphragmatic hernia using a high-resolution single-nucleotide polymorphism array
    Teshiba, Risa
    Masumoto, Kouji
    Esumi, Genshiro
    Nagata, Kouji
    Kinoshita, Yoshiaki
    Tajiri, Tatsuro
    Taguchi, Tomoaki
    Yamamoto, Ken
    PEDIATRIC SURGERY INTERNATIONAL, 2011, 27 (02) : 193 - 198
  • [50] Single nucleotide polymorphism genotyping by two colour melting curve analysis using the MGB Eclipse Probe System in challenging sequence environment.
    Belousov Y.S.
    Welch R.A.
    Sanders S.
    Mills A.
    Kulchenko A.
    Dempcy R.
    Afonina I.A.
    Walburger D.K.
    Glaser C.L.
    Yadavalli S.
    Vermeulen N.M.
    Mahoney W.
    Human Genomics, 1 (3) : 209 - 217