Ho A, Schwarze S R, Mermelstein S J, Waksman G, Dowdy S F
Howard Hughes Medical Institute and Department of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Cancer Res. 2001 Jan 15;61(2):474-7.
The protein transduction domain (PTD) embedded in the HIV TAT protein (amino acids 47-57) has been shown to successfully mediate the introduction of heterologous peptides and proteins in excess of Mr 100,000 into mammalian cells in vitro and in vivo. We report here that the modeled structure of the TAT PTD is a strong amphipathic helix. On the basis of this information, we synthesized a series of synthetic PTDs that strengthen the alpha-helical content and optimize the placement of arginine residues. Several PTD peptides possessed significantly enhanced protein transduction potential compared with TAT in vitro and in vivo. These optimized PTDs have the potential to deliver both existing and novel anticancer therapeutics.
嵌入HIV TAT蛋白(氨基酸47 - 57)中的蛋白质转导结构域(PTD)已被证明能在体外和体内成功介导将超过100,000道尔顿的异源肽和蛋白质导入哺乳动物细胞。我们在此报告,TAT PTD的模拟结构是一个强两亲性螺旋。基于此信息,我们合成了一系列合成PTD,以增强α - 螺旋含量并优化精氨酸残基的位置。与TAT相比,几种PTD肽在体外和体内具有显著增强的蛋白质转导潜力。这些优化的PTD有潜力递送现有的和新型的抗癌治疗药物。