Pathogen-specific DNA sensing with engineered zinc finger proteins immobilized on a polymer chip

被引:10
作者
Dat Thinh Ha [1 ]
Ghosh, Sthitodhi [2 ]
Ahn, Chong H. [2 ]
Segal, David J. [3 ]
Kim, Moon-Soo [1 ]
机构
[1] Western Kentucky Univ, Dept Chem, Bowling Green, KY 42101 USA
[2] Univ Cincinnati, Microsyst & BioMEMS Lab, Cincinnati, OH 45221 USA
[3] Univ Calif Davis, Dept Biochem & Mol Med, Genome Ctr, Davis, CA 95614 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
CARE CLINICAL DIAGNOSTICS; DOUBLE-STRANDED DNA; REAL-TIME PCR; BINDING PROTEINS; DESIGN; RECOGNITION; GENERATION; SEQUENCES; SELECTION; DOMAINS;
D O I
10.1039/c8an00395e
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A specific double-stranded DNA sensing system is of great interest for diagnostic and other biomedical applications. Zinc finger domains, which recognize double-stranded DNA, can be engineered to form custom DNA-binding proteins for the recognition of specific DNA sequences. As a proof of concept, a sequence-enabled reassembly of a TEM-1 -lactamase system (SEER-LAC) was previously demonstrated to develop zinc finger protein (ZFP) arrays for the detection of a double-stranded bacterial DNA sequence. Here, we implemented the SEER-LAC system to demonstrate the direct detection of pathogen-specific DNA sequences present in E. coli O157:H7 on a lab-on-a-chip. ZFPs custom-designed to detect Shiga toxin in E. coli O157:H7 were immobilized on a cyclic olefin copolymer (COC) chip, which can function as a non-PCR based molecular diagnostic device. Pathogen-specific double-stranded DNA was directly detected by using engineered ZFPs immobilized on the COC chip with high specificity, providing a detection limit of 10 fmol of target DNA in a colorimetric assay. Therefore, in this study, we demonstrated the great potential of ZFP arrays on the COC chip for further development of a simple and novel lab-on-a-chip technology for the detection of pathogens.
引用
收藏
页码:4009 / 4016
页数:9
相关论文
共 30 条
[1]   Disposable Smart lab on a chip for point-of-care clinical diagnostics [J].
Ahn, CH ;
Choi, JW ;
Beaucage, G ;
Nevin, JH ;
Lee, JB ;
Puntambekar, A ;
Lee, JY .
PROCEEDINGS OF THE IEEE, 2004, 92 (01) :154-173
[2]  
Becker H, 2000, ELECTROPHORESIS, V21, P12, DOI 10.1002/(SICI)1522-2683(20000101)21:1<12::AID-ELPS12>3.0.CO
[3]  
2-7
[4]  
Bhakta MS, 2010, METHODS MOL BIOL, V649, P3, DOI 10.1007/978-1-60761-753-2_1
[5]  
Bumgarner R, 2013, CURR PROTOC MOL BIOL, V101
[6]   An integrated dielectrophoretic chip for continuous bioparticle filtering, focusing, sorting, trapping, and detecting [J].
Cheng, I-Fang ;
Chang, Hsien-Chang ;
Hou, Diana ;
Chang, Hsueh-Chia .
BIOMICROFLUIDICS, 2007, 1 (02)
[7]   Insights into the molecular recognition of the 5′-GNN-3′ family of DNA sequences by zinc finger domains [J].
Dreier, B ;
Segal, DJ ;
Barbas, CF .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 303 (04) :489-502
[8]   Direct detection of double-stranded DNA: molecular methods and applications for DNA diagnostics [J].
Ghosh, Indraneel ;
Stains, Cliff I. ;
Ooi, Aik T. ;
Segal, David J. .
MOLECULAR BIOSYSTEMS, 2006, 2 (11) :551-560
[9]   How do site-specific DNA-binding proteins find their targets? [J].
Halford, SE ;
Marko, JF .
NUCLEIC ACIDS RESEARCH, 2004, 32 (10) :3040-3052
[10]   Multiplex Real-Time Polymerase Chain Reaction Assay for Simultaneous Detection and Quantification of Salmonella Species, Listeria monocytogenes, and Escherichia coli O157:H7 in Ground Pork Samples [J].
Kawasaki, Susumu ;
Fratamico, Pina M. ;
Horikoshi, Naoko ;
Okada, Yukio ;
Takeshita, Kazuko ;
Sameshima, Takashi ;
Kawamoto, Shinichi .
FOODBORNE PATHOGENS AND DISEASE, 2010, 7 (05) :549-554