Polyplus-transfection, R&D Department, Bd Sebastien Brant, Bioparc, P.O. Box 90018, Illkirch Cedex, 67401, France,
Cytotechnology. 2008 Jan;56(1):41-8. doi: 10.1007/s10616-007-9102-3. Epub 2007 Oct 16.
Protein delivery represents a powerful tool for experiments in live cells including studies of protein-protein interactions, protein interference with blocking antibodies, intracellular trafficking and protein or peptide biological functions. Most available reagents dedicated to the protein delivery allow efficient crossing of the plasma membrane. Nevertheless, the major disadvantage for these reagents is a weak release of the delivered protein into the cytoplasm. In this publication we demonstrate efficient protein delivery with a non-peptide based reagent, in human epithelial carcinoma HeLa cells and primary human skin fibroblasts. Using a fluorescent protein in combination with fluorescence microscopy and fluorescence-assisted cell sorting analysis, we show that the delivered protein is indeed released effectively in the cytoplasm, as expected for a dedicated carrier. Furthermore, we present a step-by-step method to optimize conditions for successful intracellular protein delivery.
蛋白质传递代表了一种在活细胞中进行实验的有力工具,包括蛋白质-蛋白质相互作用、蛋白质与阻断抗体的干扰、细胞内运输以及蛋白质或肽的生物学功能的研究。大多数可用于蛋白质传递的试剂都能有效地穿过质膜。然而,这些试剂的主要缺点是所传递的蛋白质向细胞质中的释放能力较弱。在本出版物中,我们展示了一种基于非肽的试剂在人上皮癌细胞系 HeLa 和原代人皮肤成纤维细胞中的有效蛋白质传递。通过使用荧光蛋白结合荧光显微镜和荧光辅助细胞分选分析,我们表明所传递的蛋白质确实如预期的载体那样有效地在细胞质中释放。此外,我们还提出了一种逐步优化方法,以优化成功的细胞内蛋白质传递的条件。