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Surface Plasmon Resonance Assay of Binding Properties of Antisense Oligonucleotides to Serum Albumins and Lipoproteins

机译:反义寡核苷酸与血清蛋白和脂蛋白结合特性的表面等离子体共振测定

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In the present study, we developed an assay to evaluate the kinetic binding properties of the unconjugated antisense oligonucleotide (ASO) and lipophilic and hydrophilic ligands conjugated ASOs to mouse and human serum albumin, and lipoproteins using surface plasmon resonance (SPR). The lipophilic ligands conjugated ASOs showed clear affinity to the albumins and lipoproteins, while the unconjugated and hydrophilic ligand conjugated ASOs showed no interaction. The SPR method showed reproducible immobilization of albumins and lipoproteins as ligands on the sensor chip, and reproducible affinity kinetic parameters of interaction of ASOs conjugated with the ligands could be obtained. The kinetic binding data of these ASOs to albumin and lipoproteins by SPR were related with the distributions in the whole liver in mice after administration of these conjugated ASOs. The results demonstrated that our SPR method could be a valuable tool for predicting the mechanism of the properties of delivery of conjugated ASOs to the organs.
机译:在本研究中,我们开发了一种测定,以评估未缀合的反义寡核苷酸(ASO)和亲脂和亲水性配体的动力学结合性能与小鼠和人血清白蛋白和使用表面等离子体共振(SPR)进行脂蛋白。亲脂性配体缀合的ASOS对蛋白质和脂蛋白呈现清晰的亲和力,而无缀合和亲水性配体缀合的ASOS没有相互作用。 SPR方法显示出白藜芦醇蛋白和脂蛋白作为传感器芯片上的配体的可再现固定化,并且可以获得与配体缀合的相互作用的可再现亲和力动力学参数。通过SPR通过SPR通过SPR与白蛋白和脂蛋白的动力学数据与小鼠施用这些共轭ASOS后的整个肝脏的分布有关。结果表明,我们的SPR方法可以是预测将缀合的ASO递送到器官的性质机制的有价值的工具。

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