Application of peptide nucleic acid to the direct detection of deoxyribonucleic acid amplified by polymerase chain reaction

被引:75
|
作者
Sawata, S
Kai, E
Ikebukuro, K
Iida, T
Honda, T
Karube, I
机构
[1] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
[2] Osaka Univ, Inst Microbial Dis, Dept Bacterial Infect Res, Suita, Osaka 5650871, Japan
来源
BIOSENSORS & BIOELECTRONICS | 1999年 / 14卷 / 04期
关键词
peptide nucleic acid; deoxyribonucleic acid; polymerase chain reaction;
D O I
10.1016/S0956-5663(99)00018-4
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Double-stranded DNA amplified by polymerase chain reaction (PCR) was detected by peptide nucleic acid (PNA) using a BIAcore(TM) 2000 biosensor based on surface plasmon resonance (SPR). PNA is an artificial oligo amide that is capable of forming highly stable complexes with complementary oligonucleotides. We succeeded in the direct detection of double-stranded DNA, amplified by PCR with high-sequence specificity. It was shown that the target DNA was available for detection over the range of 40-160 nM. Therefore, the detection limit was 7.5 pmol of the target DNA (143 bases, applied volume 30 mu l) Our DNA detection system, the combination of BIAcore(TM) and the probe PNA, could detect the target DNA with good reproducibility. In this report, we show that our system is a powerful tool for the diagnosis of pathologically significant DNA. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:397 / 404
页数:8
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