College of Environmental Science and Engineering, Key Laboratory of Environmental Biology and Pollution Control (Hunan University), Ministry of Education, Hunan University, Changsha 410082, China.
Analyst. 2010 Aug;135(8):2144-9. doi: 10.1039/c0an00072h. Epub 2010 Jun 28.
A bifunctional europium complex of Eu(TTA)(3)(5-NH(2)-phen) using 2-thenoyltrifluoroacetonate (TTA) and 5-amino-1,10-phenanthroline (5-NH(2)-phen) as ligand reagents was applied in DNA detection assays for the first time. The complex has a long fluorescence lifetime, high fluorescence quantum yield, and is easy to label oligonucleotides for time-resolved fluorescence bioanalysis. A two-probe tandem DNA hybridization assay including capture DNA(1), probe DNA(2), and target DNA(3) was employed to detect microbial pathogens. The DNA sequences in the assay were designed using software Primer Premier 5.0 based on published specific nucleotide sequences of Staphylococcus aureus and Escherichia coli. 3'-Amino-modified capture DNA(1) was covalently immobilized on the common glass slide surface and the 5'-amino-modified probe DNA(2) was combined with the functionalized Eu(TTA)(3)(5-NH(2)-phen) via glutaraldehyde. The detection was done by monitoring the fluorescence intensity from the glass surface after the hybridization reaction with complementary target DNA(3). The optimal concentration of capture DNA(1) of 1.0 x 10(-6) mol l(-1) dropped onto the glass slides and optimal hybridization temperatures of 48 degrees C and 39 degrees C respectively for Staphylococcus aureus and Escherichia coli were obtained. The proposed DNA detection system showed higher sensitivity than such a complex doped nanoparticle-based detection system in our previous study for the better uniformity and dispersity of monomolecular labels. The sensing system presented a short hybridization time of 2 h, satisfactory stability, and high selectivity. The results demonstrate that this complex might be a potentially excellent dye in area of biochemical analysis.
首次将 Eu(TTA)(3)(5-NH(2)-phen)(Eu(TTA)(3)(5-NH(2)-phen))的双功能铕配合物用作配体试剂,其中 TTA 为 2-噻吩甲酰三氟丙酮,5-NH(2)-phen 为 5-氨基-1,10-菲啰啉,应用于 DNA 检测分析。该配合物具有长荧光寿命、高荧光量子产率,并且易于标记寡核苷酸,可用于时间分辨荧光生物分析。采用包括捕获 DNA(1)、探针 DNA(2)和靶 DNA(3)的双探针串联 DNA 杂交测定法检测微生物病原体。测定中使用的 DNA 序列是基于金葡菌和大肠杆菌特定核苷酸序列的软件 Primer Premier 5.0 设计的。3'-氨基修饰的捕获 DNA(1)通过共价键固定在普通玻璃片表面,5'-氨基修饰的探针 DNA(2)通过戊二醛与功能化 Eu(TTA)(3)(5-NH(2)-phen)结合。通过监测与互补靶 DNA(3)杂交反应后玻璃表面的荧光强度来进行检测。获得的最佳条件为:在玻璃片上滴加 1.0 x 10(-6) mol l(-1)浓度的捕获 DNA(1),金黄色葡萄球菌和大肠杆菌的最佳杂交温度分别为 48 摄氏度和 39 摄氏度。与我们之前的研究中基于掺杂纳米粒子的复杂检测系统相比,所提出的 DNA 检测系统具有更高的灵敏度,因为单分子标记的均匀性和分散性更好。该传感系统具有较短的杂交时间(2 小时)、令人满意的稳定性和较高的选择性。结果表明,该配合物可能是生化分析领域一种有潜在优异的染料。