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一种用于活细胞荧光染色的聚氧乙烯取代双金属铕螺旋配合物。

A polyoxyethylene-substituted bimetallic europium helicate for luminescent staining of living cells.

作者信息

Chauvin Anne-Sophie, Comby Steve, Song Bo, Vandevyver Caroline D B, Thomas Frédéric, Bünzli Jean-Claude G

机构信息

Laboratory of Lanthanide Supramolecular Chemistry, Ecole Polytechnique Fédérale de Lausanne (EPFL), LCSL-BCH 1401, Switzerland.

出版信息

Chemistry. 2007;13(34):9515-26. doi: 10.1002/chem.200700883.

DOI:10.1002/chem.200700883
PMID:17879248
Abstract

The homoditopic ligand H2LC3 has been designed to form neutral triple-stranded bimetallic helicates of overall composition [Ln2(LC3)3]. The grafting of the polyoxyethylene fragments ensures water solubility and also favors cell penetration while being amenable to further derivatization. The ligand pKa values have been determined by spectrophotometric titration and range from 3.5 (sum of the first two) to 10.3. The thermodynamic stability of the helicates is large at physiological pH (logbeta23 in the range 22-23). The ligand triplet state has an adequate energy (0-phonon transition at approximately 20,800 cm(-1)) for sensitizing the luminescence of EuIII (Q=11%). Analysis of the EuIII emission spectrum points to an overall pseudo D3 symmetry for the metal environment. No significant effect of [Eu2(LC3)3] is observed on the viability of several cancerous cell lines (MCF-7, HeLa, Jurkat, and 5D10). The cell imaging properties of the EuIII helicate are demonstrated for the HeLa cell line by luminescence microscopy. Bright EuIII emission is seen for helicate concentration>50 microM and after 20-30 min loading time. The helicate stains the cytoplasm and the permeation mechanism is likely to be endocytosis.

摘要

同二齿配体H2LC3被设计用于形成总体组成为[Ln2(LC3)3]的中性三链双金属螺旋配合物。聚氧乙烯片段的接枝确保了水溶性,同时有利于细胞穿透,并且易于进一步衍生化。通过分光光度滴定法测定了配体的pKa值,范围为3.5(前两个之和)至10.3。在生理pH值下,螺旋配合物的热力学稳定性很高(logbeta23在22 - 23范围内)。配体三重态具有足够的能量(约20,800 cm(-1)处的0-声子跃迁)来敏化EuIII的发光(Q = 11%)。对EuIII发射光谱的分析表明金属环境总体上具有伪D3对称性。未观察到[Eu2(LC3)3]对几种癌细胞系(MCF-7、HeLa、Jurkat和5D10)的活力有显著影响。通过发光显微镜证明了EuIII螺旋配合物对HeLa细胞系的细胞成像特性。当螺旋配合物浓度>50 microM且加载时间为20 - 30分钟后,可看到明亮的EuIII发射。螺旋配合物使细胞质染色,渗透机制可能是内吞作用。

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