Direct colorimetric diagnosis of pathogen infections by utilizing thiol-labeled PCR primers and unmodified gold nanoparticles

被引:78
作者
Jung, Ye Lim [1 ]
Jung, Cheulhee [1 ]
Parab, Harshala [1 ]
Li, Taihua [1 ]
Park, Hyun Gyu [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea
关键词
Colorimetric detection; Nucleic acids; Gold nanoparticles; Thiol-labeled primer; Biosensors; OPTICAL-PROPERTIES; CHAIN-REACTION; NUCLEIC-ACIDS; DNA; PROBES; POLYNUCLEOTIDES; HYBRIDIZATION; AGGREGATION; COAGULATION; SEQUENCES;
D O I
10.1016/j.bios.2010.01.010
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We describe here a greatly simplified colorimetric detection method to identify PCR-amplified nucleic acids. Our method relies on the PCR product having thiol group at one end, which is generated by employing thiolated PCR primer. After PCR amplification reaction, unmodified gold nanoparticles (AuNPs) are added into the reaction tube followed by the addition of NaCl to induce the aggregation of AuNPs. The PCR products strongly bind to the surface of AuNPs through the interaction of the terminal thiol groups and the long chain of DNA which has abundant negative charges enhances the electrostatic and steric repulsion among AuNPs, which consequently leads to the prevention of the salt-induced aggregation. As a result, the color of AuNPs remains red in the presence of the PCR-amplified nucleic acids, while the AuNPs change its color from red to blue due to the salt-induced aggregation in the absence of the PCR products. This simple but very efficient colorimetric strategy was successfully demonstrated by diagnosing Chlamydia infection using a real human urine sample. Since the results can be clearly seen with the naked eye without any complicated step such as surface modification of AuNPs or PCR product purification, this method can be easily applied to point-of-care diagnosis. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1941 / 1946
页数:6
相关论文
共 38 条
[1]  
[Anonymous], 1996, Nature (London), V382, P609
[2]   Optimization of PCR based detection of human papillomavirus DNA from urine specimens [J].
Brinkman, JA ;
Rahmani, MZ ;
Jones, WE ;
Chaturvedi, AK ;
Hagensee, ME .
JOURNAL OF CLINICAL VIROLOGY, 2004, 29 (04) :230-240
[3]   Selective colorimetric detection of polynucleotides based on the distance-dependent optical properties of gold nanoparticles [J].
Elghanian, R ;
Storhoff, JJ ;
Mucic, RC ;
Letsinger, RL ;
Mirkin, CA .
SCIENCE, 1997, 277 (5329) :1078-1081
[4]   COAGULATION OF COLLOIDAL GOLD [J].
ENUSTUN, BV ;
TURKEVICH, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (21) :3317-+
[5]   Real-time PCR in clinical microbiology: Applications for a routine laboratory testing [J].
Espy, MJ ;
Uhl, JR ;
Sloan, LM ;
Buckwalter, SP ;
Jones, MF ;
Vetter, EA ;
Yao, JDC ;
Wengenack, NL ;
Rosenblatt, JE ;
Cockerill, FR ;
Smith, TF .
CLINICAL MICROBIOLOGY REVIEWS, 2006, 19 (01) :165-+
[6]   Functionalized gold nanoparticles for applications in bionanotechnology [J].
Glomm, WR .
JOURNAL OF DISPERSION SCIENCE AND TECHNOLOGY, 2005, 26 (03) :389-414
[7]   Gold nanoparticles-based protease assay [J].
Guarise, C ;
Pasquato, L ;
De Filippis, V ;
Scrimin, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (11) :3978-3982
[8]   A gold nanoparticle based approach for screening triplex DNA binders [J].
Han, MS ;
Lytton-Jean, AKR ;
Mirkin, CA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (15) :4954-4955
[9]   Reversible switching of DNA-gold nanoparticle aggregation [J].
Hazarika, P ;
Ceyhan, B ;
Niemeyer, CM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (47) :6469-6471
[10]   KINETIC PCR ANALYSIS - REAL-TIME MONITORING OF DNA AMPLIFICATION REACTIONS [J].
HIGUCHI, R ;
FOCKLER, C ;
DOLLINGER, G ;
WATSON, R .
BIO-TECHNOLOGY, 1993, 11 (09) :1026-1030