{"title":"Phosphorylatable short peptide for facilitating DNA transfection","authors":"Jingcai Ma, Xiaona Cao, Shumin Zhou, Fanqiang Kong, Yuping Ren, R. Zhao, Dong-chun Liang, Jing-yu Zhang","doi":"10.1109/FBIE.2009.5405819","DOIUrl":null,"url":null,"abstract":"A phosphorylatable short peptide(<sup>p</sup>SP) 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 <sup>p</sup>SP is the substrate of Jak2 kinase which was verified of being constantly expressed in mammalian cells. Meanwhile another kind of nonphosphorylatable <sup>np</sup>SP of “LLLRRRDNEEFGVRRLL” was also synthesized as control. Either <sup>p</sup>SP or <sup>np</sup>SP 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 <sup>p</sup>SP and hence facilitated DNA unpacking from the complex. Thereafter C2C12 mouse myoblast cells were transfected by <sup>p</sup>SP/DNA and <sup>np</sup>SP/DNA complexes respectivly and the transfection efficiency was represented by lucifersace activity in the cell lysate.","PeriodicalId":333255,"journal":{"name":"2009 International Conference on Future BioMedical Information Engineering (FBIE)","volume":"18 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2009-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2009 International Conference on Future BioMedical Information Engineering (FBIE)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/FBIE.2009.5405819","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.