促进DNA转染的可磷酸化短肽

Jingcai Ma, Xiaona Cao, Shumin Zhou, Fanqiang Kong, Yuping Ren, R. Zhao, Dong-chun Liang, Jing-yu Zhang
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引用次数: 0

摘要

化学合成了含有两个潜在可磷酸化酪氨酸残基的氨基酸组成为“LLLRRRDNEYFYVRRLL”的可磷酸化短肽(pSP)。该短肽具有等电点为10.88的特点,在生理条件下可带正电。pSP中的“DNEYFYV”基序是Jak2激酶的底物,该激酶已被证实在哺乳动物细胞中持续表达。同时合成了另一种非磷酸化npSP“LLLRRRDNEEFGVRRLL”作为对照。将pSP或npSP与含有荧光素酶报告基因的质粒DNA制成复合物。体外磷酸化和DNA释放实验表明,细胞裂解液可以磷酸化pSP,从而促进DNA从复合物中解包。然后分别用pSP/DNA和npSP/DNA复合物转染C2C12小鼠成肌细胞,用细胞裂解液中的荧光素酶活性来表示转染效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phosphorylatable short peptide for facilitating DNA transfection
A phosphorylatable short peptide(pSP) with the amino acid composition of “LLLRRRDNEYFYVRRLL” containing two potentially phosphorylatable tyrosine residues was chemically synthesized. This short peptide was characteristic with the isoelectric point of 10.88 and could be positively charged under physiological condition. The “DNEYFYV” motif in the pSP is the substrate of Jak2 kinase which was verified of being constantly expressed in mammalian cells. Meanwhile another kind of nonphosphorylatable npSP of “LLLRRRDNEEFGVRRLL” was also synthesized as control. Either pSP or npSP was made into complex with plasmid DNA containing luciferase reporter gene. In vitro phosphorylation and DNA releasing assays demonstrated that cell lysate could phosphorylated the pSP and hence facilitated DNA unpacking from the complex. Thereafter C2C12 mouse myoblast cells were transfected by pSP/DNA and npSP/DNA complexes respectivly and the transfection efficiency was represented by lucifersace activity in the cell lysate.
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