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DARTs: A DNA-based in vitro polypeptide display technology

机译:DARTs:一种基于DNA的体外多肽展示技术

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Display technologies link proteins with the genes that encode them, providing a means of selecting proteins with desired properties through the process of directed evolution. Here, we describe DNA/protein attachment and recovery tools (DARTs), a novel polypeptide display technology that utilizes the Agrobacterium tumefaciens protein VirD2 to generate DNA-protein hybrid molecules. The resulting DNA-protein hybrids are small, robust, and are not expected to be subject to the synthesis and selection biases associated with viral- and cell-based display systems. We demonstrated that these DNA-protein hybrids could be used to display a variety of peptides that bind to appropriate antibodies for immunodetection and immuno-purification. Further, the DNA components of the hybrid molecules can hybridize to complementary DNA molecules in solution or on a solid substrate. Because full-length VirD2 self-associated, we constructed a truncation that did not self-associate but still exhibited DNA linking activity and efficiently displayed peptides. Finally, we purified DNA-protein hybrids using their displayed peptide epitopes and amplified their DNA components by polymerase chain reaction. We suggest that the DART polypepticle display system will be valuable for performing directed evolution and generating protein arrays.
机译:展示技术将蛋白质与编码蛋白质的基因联系起来,从而提供了一种通过定向进化过程选择具有所需特性的蛋白质的方法。在这里,我们描述了DNA /蛋白质附着和恢复工具(DART),这是一种利用根癌土壤杆菌蛋白质VirD2产生DNA-蛋白质杂合分子的新型多肽展示技术。所得的DNA-蛋白质杂种较小,坚固,并且不会受到与基于病毒和细胞的展示系统相关的合成和选择偏见的影响。我们证明了这些DNA-蛋白质杂合体可用于展示与适当抗体结合以进行免疫检测和免疫纯化的各种肽。此外,杂合分子的DNA组分可以在溶液中或在固体底物上与互补DNA分子杂交。因为全长VirD2是自缔合的,所以我们构建了一个不自缔合但仍表现出DNA连接活性并有效展示肽的截短体。最后,我们使用展示的肽表位纯化了DNA-蛋白质杂种,并通过聚合酶链反应扩增了其DNA成分。我们建议DART多菌灵展示系统对于进行定向进化和生成蛋白质阵列将是有价值的。

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