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Completely Monodisperse, Highly Repetitive Proteins for Bioconjugate Capillary Electrophoresis: Development and Characterization

机译:用于生物缀合物毛细管电泳的完全单分散,高度重复的蛋白质:开发和表征

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Protein-based polymers are increasingly being used in biomaterial applications because of their ease of customization and potential monodispersity. These advantages make protein polymers excellent candidates for bioanalytical applications. Here we describe improved methods for producing drag-tags for free-solution conjugate electrophoresis (FSCE). FSCE utilizes a pure, monodisperse recombinant protein, tethered end-on to a ssDNA molecule, to enable DNA size separation in aqueous buffer. FSCE also provides a highly sensitive method to evaluate the polydispersity of a protein drag-tag and thus its suitability for bioanalytical uses. This method is able to detect slight differences in drag-tag charge or mass. We have devised an improved cloning, expression, and purification strategy that enables us to generate, for the first time, a truly monodisperse 20 kDa protein polymer and a nearly monodisperse 38 kDa protein. These newly produced proteins can be used as drag-tags to enable longer read DNA sequencing by free-solution microchannel electrophoresis.
机译:基于蛋白质的聚合物因易于定制和潜在的单分散性而越来越多地用于生物材料应用中。这些优点使蛋白质聚合物成为生物分析应用的极佳候选者。在这里,我们描述了改进的方法,以产生用于自由溶液共轭电泳(FSCE)的标签。 FSCE利用纯净的单分散重组蛋白,末端固定在ssDNA分子上,从而能够在水性缓冲液中分离DNA大小。 FSCE还提供了一种高度敏感的方法来评估蛋白质药物标签的多分散性,从而评估其在生物分析中的适用性。这种方法能够检测出标签电荷或质量的细微差异。我们设计了一种改进的克隆,表达和纯化策略,使我们能够首次生成真正单分散的20 kDa蛋白聚合物和几乎单分散的38 kDa蛋白。这些新产生的蛋白质可以用作标签,通过自由溶液微通道电泳实现更长的读取DNA测序。

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