1] Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas, USA. [2].
Department of Biochemistry and Biophysics, Texas A&M University, College Station, Texas, USA.
Nat Methods. 2014 Aug;11(8):861-7. doi: 10.1038/nmeth.2998. Epub 2014 Jun 15.
We report that a tetramethylrhodamine-labeled dimer of the cell-penetrating peptide TAT, dfTAT, penetrates live cells by escaping from endosomes with high efficiency. By mediating endosomal leakage, dfTAT also delivers proteins into cultured cells after a simple co-incubation procedure. We achieved cytosolic delivery in several cell lines and primary cells and observed that only a relatively small amount of material remained trapped inside endosomes. Delivery did not require a binding interaction between dfTAT and a protein, multiple molecules could be delivered simultaneously, and delivery could be repeated. dfTAT-mediated delivery did not noticeably affect cell viability, cell proliferation or gene expression. dfTAT-based intracellular delivery should be useful for cell-based assays, cellular imaging applications and the ex vivo manipulation of cells.
我们报告称,一种四甲基罗丹明标记的细胞穿透肽 TAT 的二聚体 dfTAT 通过高效逃离内体进入活细胞。通过介导内体泄漏,dfTAT 还可以在简单的共孵育后将蛋白质递送到培养细胞中。我们在几种细胞系和原代细胞中实现了细胞质递送,并且观察到只有相对少量的物质仍然被困在内体中。递呈不需要 dfTAT 与蛋白质之间的结合相互作用,可以同时递呈多个分子,并且可以重复递呈。dfTAT 介导的递呈不会明显影响细胞活力、细胞增殖或基因表达。基于 dfTAT 的细胞内递呈应该对基于细胞的测定、细胞成像应用和细胞的离体操作有用。