Kida Shinya, Eto Yusuke, Yoshioka Yasuo, Nakagawa Shinsaku, Kawasaki Koichi, Maeda Mitsuko
Life Science Center, Faculty of Pharmaceutical Sciences, Kobe Gakuin University, Minatojima, Chuo-ku, Kobe 650-8586, Japan.
Protein Pept Lett. 2010 Feb;17(2):164-7. doi: 10.2174/092986610790225978.
Two cell-penetrating peptides, a Pro-rich peptide derivative, acetyl-(Val-Arg-Leu-Pro-Pro-Pro)(3)-Gly-Cys amide, and an octaarginine derivative, acetyl-Arg-Arg-Arg-Arg-Arg-Arg-Arg-Arg-Gly-Cys amide, were prepared by the solid phase method. Each peptide was coupled to the heterobifunctional cross-linking reagent, 6-maleimidohexanoic acid N-hydroxysuccinimide ester, and then conjugated to the Adenovirus vector containing luciferase gene. Peptide-modified Ad, as compared with wild-type Ad, exhibited excellent luciferase activity in B16BL6 cells.
通过固相法制备了两种细胞穿透肽、一种富含脯氨酸的肽衍生物乙酰基-(缬氨酸-精氨酸-亮氨酸-脯氨酸-脯氨酸-脯氨酸)₃-甘氨酸-半胱氨酸酰胺以及一种八聚精氨酸衍生物乙酰基-精氨酸-精氨酸-精氨酸-精氨酸-精氨酸-精氨酸-精氨酸-精氨酸-甘氨酸-半胱氨酸酰胺。将每种肽与异双功能交联剂N-羟基琥珀酰亚胺基6-马来酰亚胺己酸酯偶联,然后与含有荧光素酶基因的腺病毒载体缀合。与野生型腺病毒相比,肽修饰的腺病毒在B16BL6细胞中表现出优异的荧光素酶活性。