A DNA aptamer with high affinity and specificity for therapeutic anthracyclines

被引:81
|
作者
Wochner, Aniela [1 ,2 ]
Menger, Marcus [1 ]
Orgel, Dagmar [1 ]
Cech, Birgit [1 ]
Rimmele, Martina [1 ]
Erdmann, Volker A. [2 ]
Gloekler, Joern [1 ]
机构
[1] RiNA Netzwerk RNA Technol, D-14195 Berlin, Germany
[2] Free Univ Berlin, Dept Biochem, D-14195 Berlin, Germany
关键词
DNA aptamer; daunomycin; doxorubicin; in vitro selection; SELEX; competition assay;
D O I
10.1016/j.ab.2007.09.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe the characterization of a DNA aptamer that displays high affinity and specificity for the anthracyclines daunomycin and doxorubicin, both of which are frequently used in chemotherapy. Aptamers were isolated from a pool of random sequences using a semi-automated procedure for magnetic beads. All selected aptamers displayed high affinity for the target molecule daunomycin. One aptamer was further characterized and exhibited a dissociation constant (K-D) of 20 nM. To examine the aptamer's binding properties and clarify its applicability for diagnostic assays, its performance under various buffer conditions was evaluated. The aptamer proved to be very robust and not dependent on the presence of specific ions. It also tolerated a wide pH range and immobilization via 5'-biotinylation. Furthermore, a competition assay for sensitive daunomycin detection was established. This not only allows the determination of the aptamer's specificity but also allows the quantification of as little as 8.4 mu g/L daunomycin and doxorubicin. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:34 / 42
页数:9
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