Proximity extension of circular DNA aptamers with real-time protein detection

被引:158
作者
Di Giusto, DA
Wlassoff, WA
Gooding, JJ
Messerle, BA
King, GC [1 ]
机构
[1] Univ New S Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会;
关键词
D O I
10.1093/nar/gni063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Multivalent circular aptamers or 'captamers' have recently been introduced through the merger of aptameric recognition functions with the basic principles of DNA nanotechnology. Aptamers have strong utility as protein-binding motifs for diagnostic applications, where their ease of discovery, thermal stability and low cost make them ideal components for incorporation into targeted protein assays. Here we report upon a property specific to circular DNA aptamers: their intrinsic compatibility with a highly sensitive protein detection method termed the 'proximity extension' assay. The circular DNA architecture facilitates the integration of multiple functional elements into a single molecule: aptameric target recognition, nucleic acid hybridization specificity and rolling circle amplification. Successful exploitation of these properties is demonstrated for the molecular analysis of thrombin, with the assay delivering a detection limit nearly three orders of magnitude below the dissociation constants of the two contributing aptamer-thrombin interactions. Real-time signal amplification and detection under isothermal conditions points towards potential clinical applications, with both fluorescent and bioelectronic methods of detection achieved. This application elaborates the pleiotropic properties of circular DNA aptamers beyond the stability, potency and multitargeting characteristics described earlier.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 56 条
[1]   Synthesis of the first ferrocene-labeled dideoxynucleotide and its use for 3′-redox end-labeling of 5′-modified single-stranded oligonucleotides [J].
Anne, A ;
Blanc, B ;
Moiroux, J .
BIOCONJUGATE CHEMISTRY, 2001, 12 (03) :396-405
[2]   Signal amplification of padlock probes by rolling circle replication [J].
Banér, J ;
Nilsson, M ;
Mendel-Hartvig, M ;
Landegren, U .
NUCLEIC ACIDS RESEARCH, 1998, 26 (22) :5073-5078
[3]   SELECTION OF SINGLE-STRANDED-DNA MOLECULES THAT BIND AND INHIBIT HUMAN THROMBIN [J].
BOCK, LC ;
GRIFFIN, LC ;
LATHAM, JA ;
VERMAAS, EH ;
TOOLE, JJ .
NATURE, 1992, 355 (6360) :564-566
[4]   DNA-templated assembly and electrode attachment of a conducting silver wire [J].
Braun, E ;
Eichen, Y ;
Sivan, U ;
Ben-Yoseph, G .
NATURE, 1998, 391 (6669) :775-778
[5]   Use of an electrochemically labeled nucleotide terminator for known point mutation analysis [J].
Brazill, S ;
Hebert, NE ;
Kuhr, WG .
ELECTROPHORESIS, 2003, 24 (16) :2749-2757
[6]   A single base extension technique for the analysis of known mutations utilizing capillary gel electrophoreisis with electrochemical detection [J].
Brazill, SA ;
Kuhr, WG .
ANALYTICAL CHEMISTRY, 2002, 74 (14) :3421-3428
[7]  
Brody E N, 2000, J Biotechnol, V74, P5, DOI 10.1016/S1389-0352(99)00004-5
[8]   In vitro selection of DNA aptamers to anthrax spores with electrochemiluminescence detection [J].
Bruno, JG ;
Kiel, JL .
BIOSENSORS & BIOELECTRONICS, 1999, 14 (05) :457-464
[9]  
Butenas S, 2002, BIOCHEMISTRY-MOSCOW+, V67, P3
[10]   Putting a brake on an autonomous DNA nanomotor [J].
Chen, Y ;
Mao, CD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (28) :8626-8627