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Evaluation of RNA-binding specificity of aminoglycosides with DNA microarrays

机译:用DNA微阵列评估氨基糖苷的RNA结合特异性

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We have developed methods for using DNA array technology to probe the entire transcriptome to determine the RNA-binding specificity of ligands. Two methods were investigated. in the first method, the RNA-binding aminoglycoside antibiotic tobramycin was covalently linked to magnetic beads. The beads were bound to human liver mRNA and washed, and specifically bound RNA was eluted, amplified, and analyzed with DNA array technology. A small number of genes were found to bind specifically to the tobramycin beads. In the second method, the aminoglycoside ligand was added directly to the array hybridization reaction, and the signal was compared with a control experiment in the absence of ligand. The aminoglycosides were found to interfere with a small percentage of all hybridization events. These methods differ from traditional DNA array experiments in that the readout is a direct measure of,the interaction between mRNA and a ligand, rather than an indirect measure of effect on expression. We expect that the results will lead to the discovery of new aminoglycoside-binding RNA motifs and may also have relevance toward understanding and overcoming the side effects observed with these antibiotics in the clinic.
机译:我们已经开发出了使用DNA阵列技术探测整个转录组以确定配体RNA结合特异性的方法。研究了两种方法。在第一种方法中,将结合RNA的氨基糖苷抗生素妥布霉素与磁珠共价连接。将珠子与人肝mRNA结合并洗涤,然后将特异性结合的RNA洗脱,扩增并用DNA阵列技术进行分析。发现少数基因与妥布霉素珠特异性结合。在第二种方法中,将氨基糖苷配体直接添加到阵列杂交反应中,并将信号与不存在配体的对照实验进行比较。发现氨基糖苷干扰所有杂交事件的一小部分。这些方法与传统的DNA阵列实验的不同之处在于,读数是mRNA和配体之间相互作用的直接量度,而不是对表达影响的间接量度。我们希望该结果将导致发现新的结合氨基糖苷的RNA图案,并且可能与理解和克服在临床中使用这些抗生素所观察到的副作用有关。

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