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Data on G-quadruplex topology, and binding ability of G-quadruplex forming sequences found in the promoter region of biomarker proteins and those relations to the presence of nuclear localization signal in the proteins

机译:关于G-Quadreplex拓扑的数据,以及生物标志物蛋白的启动子区域中发现的G-Quadflex形成序列的结合能力以及蛋白质中存在核定位信号的关系

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摘要

Aptamer is a nucleic acid ligand which specifically binds to its target molecule. Previously, we have designed an identification method of aptamer called “G-quadruplex (G4) promoter-derived aptamer selection (G4PAS)” . In G4PAS procedure, putative G4 forming sequences (PQS) were explored in a promoter region of a target protein in human gene through computational analysis, and evaluated binding ability towards the gene product encoded in the downstream of the promoter. We investigated the topology of the obtained PQSs by circular dichroism measurement, as well as their binding ability against its target protein by surface plasmon resonance measurement and gel-shift assay. Additionally, the presence of nuclear localization signal in the target protein was predictedin silico. This data set summarized all the PQS sequences, their biochemical characteristics, and the presence of nuclear localization signal to address the possibility of binding of these PQS region to the target proteinsin vivo. Those data should contribute to increase the success rate of G4PAS. Moreover, considering the G4 motifs in genomic DNA are suggested to be involvedin vivogene regulation , this data set is also potentially beneficial for the cell biology field.
机译:适体是核酸配体,其特异性结合其靶分子。以前,我们设计了一种名为“G-Quadruplex(G4)启动子推导的适体选择(G4PAS)”的适体的识别方法。在G4Pas过程中,通过计算分析在人基因的靶蛋白的启动子区中探讨推定的G4形成序列(PQs),并评估朝向启动子下游编码的基因产物的结合能力。我们通过圆形二色性测量研究了所获得的PQSS的拓扑,以及通过表面等离子体共振测量和凝胶转移测定对其靶蛋白的结合能力。另外,靶蛋白中核定位信号的存在是预测的硅片。该数据集总结了所有PQS序列,其生化特征和核定位信号的存在,以解决将这些PQS区域结合到目标蛋白体内的可能性。这些数据应该有助于提高G4PAS的成功率。此外,考虑到基因组DNA中的G4基序被提出参与体育促例,该数据集也可能对细胞生物学领域有益。

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