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使用实时监测技术对细胞摄取和转导的体内追踪进行定量分析。

Quantification of cellular uptake and in vivo tracking of transduction using real-time monitoring.

机构信息

Division of Bio-Imaging, Chuncheon Center, Korea Basic Science Institute, Chuncheon, Kangwon-Do 200-701, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2010 Apr 2;394(2):348-53. doi: 10.1016/j.bbrc.2010.03.009. Epub 2010 Mar 4.

Abstract

Protein transduction domains (PTDs) are short amino acid sequences that promote their own translocation across the cell plasma membrane and have been studied for possible use in drug delivery and gene therapy. However, no direct method to quantify transduction is available. Here, using a new luciferase-tagged human PTD, we show that cellular uptake levels can be determined in a reliable manner. Furthermore, we show that enhanced in vivo tracking by human PTD can be quantified in a mouse model. This is the first report on the direct quantification of PTD transduction in vitro and in vivo, which will be necessary for studying its possible therapeutic application in drug delivery and gene therapy.

摘要

蛋白转导结构域(PTDs)是一些短的氨基酸序列,可以促进它们自身穿过细胞质膜的转运,已经被研究用于药物输送和基因治疗。然而,目前还没有直接的方法来定量转导。在这里,我们使用一种新的荧光素酶标记的人源 PTD,显示了可以可靠地确定细胞摄取水平。此外,我们还显示,在小鼠模型中可以定量增强的体内跟踪。这是第一个关于 PTD 体外和体内转导的直接定量的报告,这对于研究其在药物输送和基因治疗中的潜在治疗应用是必要的。

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