Isolation and characterization of DNA aptamers against Escherichia coli using a bacterial cell-systematic evolution of ligands by exponential enrichment approach

被引:92
作者
Kim, Yeon Seok [1 ]
Song, Min Young [1 ]
Jurng, Jongsoo [1 ]
Kim, Byoung Chan [1 ]
机构
[1] Korea Inst Sci & Technol, Ctr Environm Hlth & Welf Res, Seoul 136701, South Korea
关键词
Bacteria cell-SELEX; DNA aptamers; E; coli; Fluorescence; SWITCHING SIGNALING APTAMERS; IN-VITRO; SELECTION; SEQUENCE; BINDING; MOLECULES; STRATEGIES; PATHOGENS; SAMPLES;
D O I
10.1016/j.ab.2013.01.014
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aptamers are powerful capturing probes against various targets such as proteins, small organic compounds, metal ions, and even cells. In this study, we isolated and characterized single-stranded DNA (ssDNA) aptamers against Escherichia coli. A total of 28 ssDNAs were isolated after 10 rounds of selection using a bacterial cell-SELEX (systematic evolution of ligands by exponential enrichment) process. Other bacterial species (Klebsiella pneumoniae, Citrobacter freundii, Enterobacter aerogenes, and Staphylococcus epidermidis) were used for counter selection to enhance the selectivity of ssDNA aptamers against E. coli. Finally, four ssDNA aptamers showed high affinity and selectivity to E. coli, The dissociation constants (K-d) of these four ssDNA aptamers to E. coli were estimated to range from 12.4 to 25.2 nM. These aptamers did not bind to other bacterial species, including four counter cells, but they showed affinity to different E. coli strains. The binding of these four aptamers to E. coli was observed directly by fluorescence microscopy. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:22 / 28
页数:7
相关论文
共 36 条
[11]   INVITRO SELECTION OF RNA MOLECULES THAT BIND SPECIFIC LIGANDS [J].
ELLINGTON, AD ;
SZOSTAK, JW .
NATURE, 1990, 346 (6287) :818-822
[12]   Massively Parallel Interrogation of Aptamer Sequence, Structure and Function [J].
Fischer, Nicholas O. ;
Tok, Jeffrey B. -H. ;
Tarasow, Theodore M. .
PLOS ONE, 2008, 3 (07)
[13]   Biofunctional magnetic nanoparticles for protein separation and pathogen detection [J].
Gu, HW ;
Xu, KM ;
Xu, CJ ;
Xu, B .
CHEMICAL COMMUNICATIONS, 2006, (09) :941-949
[14]   Selection and analytical applications of aptamers binding microbial pathogens [J].
Hamula, Camille L. A. ;
Zhang, Hongquan ;
Li, Feng ;
Wang, Zhixin ;
Le, X. Chris ;
Li, Xing-Fang .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2011, 30 (10) :1587-1597
[15]   Influence of ionic strength, pH and aptamer configuration for binding affinity to thrombin [J].
Hianik, Tibor ;
Ostatna, Veronika ;
Sonlajtnerova, Michaela ;
Grman, Igor .
BIOELECTROCHEMISTRY, 2007, 70 (01) :127-133
[16]  
Jayasena SD, 1999, CLIN CHEM, V45, P1628
[17]   Exploring the sequence space of a DNA aptamer using microarrays [J].
Katilius, Evaldas ;
Flores, Carole ;
Woodbury, Neal W. .
NUCLEIC ACIDS RESEARCH, 2007, 35 (22) :7626-7635
[18]   Interaction of three-way DNA junctions with steroids [J].
Kato, T ;
Yano, K ;
Ikebukuro, K ;
Karube, I .
NUCLEIC ACIDS RESEARCH, 2000, 28 (09) :1963-1968
[19]   Active site binding and sequence requirements for inhibition of HIV-1 reverse transcriptase by the RT1 family of single-stranded DNA aptamers [J].
Kissel, Jay D. ;
Held, Daniel M. ;
Hardy, Richard W. ;
Burke, Donald H. .
NUCLEIC ACIDS RESEARCH, 2007, 35 (15) :5039-5050
[20]   Advances in the bacteriology of the Coliform Group: Their suitability as markers of microbial water safety [J].
Leclerc, H ;
Mossel, DAA ;
Edberg, SC ;
Struijk, CB .
ANNUAL REVIEW OF MICROBIOLOGY, 2001, 55 :201-234