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Synthesis of cell-penetrating S-galactosyl-oligoarginine peptides as inducers of recombinant protein expression under the control of lac operator/repressor systems

机译:在LAC操作员/阻遏物系统控制下,合成细胞穿透性S-半乳糖基 - 寡糖肽作为重组蛋白表达的诱导剂

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摘要

The synthesis of glycodendrimers and glycopoly(oxazoline)s as inducers of recombinant protein expression has recently been reported; however, these compounds induced the expression of only small amounts of the green fluorescence protein (GFP), which was used as the model recombinant protein, because of their poor ability to penetrate the Escherichia coli cell membrane. Therefore, S-galactosyl-oligo(Arg) conjugates have now been synthesized to overcome this problem. Following in vivo expression of GFP induced by each of the S-galactosyl (Arg)n constructs (n=5, 6, 8) at the T5 promoter in E. coli for 18 hours, we visually observed that the cultures fluoresced green light when excited with UV light. The fluorescent intensities for these cultures were greater than that found for a control culture, which indicates that the peptides had induced GFP expression. Quantitative fluorescent measurements also supported the observations that the peptides were better inducers of GFP expression than the galactosyl dendrimers and the poly(oxazoline)s and the natural inducer lactose. Because the level of GFP expression was directly related to the number of arginine moieties in each peptide, we propose that the number of arginine moieties is responsible for how well each peptide passes through the E. coli membrane, which affects the expression level. A similar tendency was observed when the T7 promoter was placed upstream from the gene for an artificial extracellular matrix protein and the S-Gal-oligo(Arg) peptides were used as inducers. To assess how the distance between two galactosyl moieties as well as how the multivalent effect (cluster effect) in an oligo(Arg) inducer affects the expression level of GFP, we synthesized a conjugate of Lys(Arg)8 (Lys=lysine) and two S-galactosyls, which enhanced the expression of GFP in comparison with that obtained for S-Gal(Arg)8.
机译:六甘油偶联剂和甘唑啉(恶唑啉)的合成最近据报道为重组蛋白表达的诱导剂;然而,这些化合物仅诱导了仅使用作为模型重组蛋白的绿色荧光蛋白(GFP)的表达,因为它们渗透了大肠杆菌细胞膜的能力差。因此,现在已经合成了S-半乳糖基 - 寡核苷酸(Arg)缀合物以克服这个问题。在大肠杆菌中T5启动子的每个S-半乳糖基(Arg)N构建体(N = 5,6,8)的GFP的体内表达18小时后,我们在视觉上观察到培养物荧光时用紫外线闪光。这些培养物的荧光强度大于对照培养物的荧光强度,这表明肽诱导了GFP表达。定量荧光测量还支持观察结果,即肽是GFP表达的更好的诱导剂,而不是半乳糖基树枝状大分子和聚(恶唑啉)和天然诱导剂乳糖。由于GFP表达的水平与每种肽中的精氨酸部分的数量直接相关,所以我们提出了精氨酸部分的数量对每个肽通过大肠杆菌膜的数量负责影响表达水平的大肠杆菌膜。当将T7启动子置于置于人造细胞外基质蛋白的基因上游时,观察到类似的趋势,并且使用S-Gal-oligo(Arg)肽作为诱导剂。评估两种半乳糖基部分之间的距离以及如何在寡核苷酸(ARG)诱导物中的多价效应(簇效应)影响GFP的表达水平,我们合成Lys(Arg)8(Lys =赖氨酸)的缀合物(Lys =赖氨酸)和与S-GAL(ARG)8获得的相比,两个S-半乳糖基,其增强了GFP的表达。

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  • 来源
    《ChemPlusChem》 |2013年第7期|共7页
  • 作者

    MizutaY.; TakasuA.; HiguchiM.;

  • 作者单位

    Department of Frontier Materials Nagoya Institute of Technology Gokiso-Cho Showa-Ku Nagoya 466;

    Department of Frontier Materials Nagoya Institute of Technology Gokiso-Cho Showa-Ku Nagoya 466;

    Department of Frontier Materials Nagoya Institute of Technology Gokiso-Cho Showa-Ku Nagoya 466;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

    bacteria; biosynthesis; fluorescence; glycopeptides; protein expression;

    机译:细菌;生物合成;荧光;糖肽;蛋白表达;

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