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首页> 外文期刊>Molecular therapy: the journal of the American Society of Gene Therapy >Labeling and intracellular tracking of functionally active plasmid DNA with semiconductor quantum dots.
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Labeling and intracellular tracking of functionally active plasmid DNA with semiconductor quantum dots.

机译:具有半导体量子点的功能活性质粒DNA的标记和细胞内跟踪。

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Semiconductor nanocrystal quantum dots (QDs) allow long-term imaging in the cellular environment with high photostability. QD biolabeling techniques have previously been developed for tagging proteins and peptides as well as oligonucleotides. In this contribution, QD-decorated plasmid DNA was utilized for the first time for long-term intracellular and intranuclear tracking studies. Conjugation of plasmid DNA with phospholipid-coated QDs was accomplished using a peptide nucleic acid (PNA)-N-succinimidyl-3-(2-pyridylthio) propionate linker. Gel electrophoresis and confocal and atomic force microscopy (AFM) were used to confirm the structure of QD-DNA conjugates. AFM imaging also revealed that multiple QDs were attached in a cluster at the PNA-reactive site of the plasmid DNA. These QD-DNA conjugates were capable of expressing the reporter protein, enhanced green fluorescent protein, following transfection in Chinese hamster ovary (CHO-K1) cells with an efficiency of ca. 62%, which was comparable to the control (unconjugated) plasmid DNA.
机译:半导体纳米晶体量子点(QD)允许在细胞环境中以高光稳定性进行长期成像。先前已经开发出QD生物标记技术来标记蛋白质和肽以及寡核苷酸。在这种贡献中,QD修饰的质粒DNA首次用于长期的细胞内和核内跟踪研究。使用肽核酸(PNA)-N-琥珀酰亚胺基-3-(2-吡啶硫基)丙酸酯连接子实现质粒DNA与磷脂包被的QD的缀合。凝胶电泳,共聚焦和原子力显微镜(AFM)被用于确认QD-DNA共轭物的结构。原子力显微镜成像还显示,多个QD簇状连接在质粒DNA的PNA反应位点。这些QD-DNA偶联物在转染到中国仓鼠卵巢(CHO-K1)细胞后,能够表达报告蛋白,增强的绿色荧光蛋白,效率约为。 62%,与对照(未缀合的)质粒DNA相当。

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