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Submicrometer Nanospray Emitters Provide New Insights into the Mechanism of Cation Adduction to Anionic Oligonucleotides

机译:亚细仪纳米普雷发射器为阴离子寡核苷酸的阳离子含量提供了新的见解

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The electrospray-MS analysis of oligonucleotides is hampered by nonvolatile metal cations, which may produce adducts responsible for signal suppression and loss of resolution. Alternative to replacing metal cations with MS-friendly ammonium, we explored the utilization of nanospray emitters with submicrometer-diameter tips, which was shown to benefit the analysis of protein samples containing elevated salt concentrations. We demonstrated that such benefits are not limited to proteins, but extend also to oligonucleotide samples analyzed in the negative ion mode. At elevated Na+/Mg2+ concentrations, submicrometer tips produced significantly greater signal-to-noise ratios, as well as greatly reduced adducts and salt clusters, than observed when utilizing micrometer tips. These effects were marginally affected by emitter composition (i.e., borosilicate versus quartz), but varied according to salt concentration and number of oligonucleotide phosphates. The results confirmed that adduct formation is driven by the concentrating effects of the desolvation process, which leads to greatly increased solute concentrations as the volume of the droplet decreases. The process promotes cation-phosphate interactions that may not have necessarily existed in the initial sample, but nevertheless shape the observed adduct series. Therefore, such series may not accurately reflect the distribution of counterions surrounding the analyte in solution. No adverse effects were noted on specific metal interactions, such as those present in a model drug DNA assembly. These observations indicate that the utilization of submicrometer tips represents an excellent alternative to traditional ammonium-replacement approaches, which enables the analysis of oligonucleotides in the presence of Na+/Mg2+ concentrations capable of preserving their structure and functional properties.
机译:通过非挥发性金属阳离子阻碍了寡核苷酸的电喷雾-Sm MS分析,其可以产生负责的加合物,该加合物用于信号抑制和分辨率的损失。替代用MS友好铵替代金属阳离子的替代物,我们探讨了利用亚型直径提示的纳米粥发射器,其显示有利于含有含盐浓度升高的蛋白质样品的分析。我们证明这种益处不限于蛋白质,而是延伸到在负离子模式中分析的寡核苷酸样品。在升高的Na + / mg2 +浓度下,亚微米计提示产生明显更大的信噪比,以及在利用千分尺尖端时观察到的加合物和盐簇的大大减少。这些效果由发射器组合物(即,硼硅酸盐与石英)略微影响,但根据盐浓度和寡核苷酸磷酸酯的数量而变化。结果证实,加合物形成通过脱溶解方法的浓缩效果驱动,这导致大大增加溶质浓度,因为液滴的体积减小。该方法促进可能在初始样品中不一定存在的阳离子 - 磷酸酯相互作用,但仍然是观察到的加合物系列。因此,这种系列可能无法准确反映溶液中分析物周围的抗衡离子的分布。在特定的金属相互作用上没有注意到不利影响,例如模型药物DNA组件中存在的那些。这些观察结果表明,潜脑提示的利用代表了传统铵替代方法的优异替代方案,其能够在纳+ / Mg2 +浓度存在下进行寡核苷酸,能够保持其结构和功能性质。

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