Schwarze S R, Hruska K A, Dowdy S F
Howard Hughes Medical Institute, Depts of Pathology and Medicine, and Barnes-Jewish Hospital, Washington University School of Medicine, 4940 Parkview Place, Campus Box 8022, St Louis, MO 63110, USA.
Trends Cell Biol. 2000 Jul;10(7):290-5. doi: 10.1016/s0962-8924(00)01771-2.
Several proteins can traverse biological membranes through protein transduction. Small sections of these proteins (10-16 residues long) are responsible for this. Linking these domains covalently to compounds, peptides, antisense peptide nucleic acids or 40-nm iron beads, or as in-frame fusions with full-length proteins, lets them enter any cell type in a receptor- and transporter-independent fashion. Moreover, several of these fusions, introduced into mice, were delivered to all tissues, even crossing the blood-brain barrier. These domains thus might let us address new questions and even help in the treatment of human disease.
几种蛋白质可通过蛋白质转导穿过生物膜。这些蛋白质的小片段(长度为10 - 16个残基)负责此功能。将这些结构域与化合物、肽、反义肽核酸或40纳米铁珠共价连接,或与全长蛋白质进行读码框内融合,可使其以不依赖受体和转运体的方式进入任何细胞类型。此外,将其中几种融合蛋白导入小鼠体内后,它们会被递送至所有组织,甚至能够穿过血脑屏障。因此,这些结构域或许能让我们解决新问题,甚至有助于人类疾病的治疗。