Department of Chemistry , University at Albany , Albany , New York 12222 , United States.
Department of Chemistry , University of California-Berkeley , Berkeley , California 94720-1460 , United States.
Anal Chem. 2018 Nov 20;90(22):13541-13548. doi: 10.1021/acs.analchem.8b03632. Epub 2018 Nov 5.
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/Mg 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/Mg concentrations capable of preserving their structure and functional properties.
寡核苷酸的电喷雾-MS 分析受到非挥发性金属阳离子的阻碍,这些阳离子可能会产生加合物,导致信号抑制和分辨率降低。我们探索了用 MS 友好的铵替代金属阳离子的方法,而不是用亚微米直径尖端的纳米喷雾发射器替代,事实证明,这种方法有利于分析含有高盐浓度的蛋白质样品。我们证明,这种好处不仅限于蛋白质,而且还扩展到了负离子模式下分析的寡核苷酸样品。在升高的 Na/Mg 浓度下,与使用微米尖端相比,亚微米尖端产生了显著更高的信噪比,以及大大减少的加合物和盐簇。这些效应受发射器组成(即硼硅酸盐与石英)的影响较小,但根据盐浓度和寡核苷酸磷酸基数而变化。结果证实,加合物的形成是由去溶剂化过程的浓缩效应驱动的,随着液滴体积的减小,溶质浓度大大增加。该过程促进了阳离子-磷酸根相互作用,这些相互作用在初始样品中可能不一定存在,但仍会影响观察到的加合物系列。因此,这些系列可能无法准确反映分析物在溶液中周围抗衡离子的分布。在特定金属相互作用(例如模型药物-DNA 组装中的相互作用)方面未观察到不利影响。这些观察结果表明,亚微米尖端的使用代表了传统铵替代方法的极好替代方法,能够在能够保持其结构和功能特性的 Na/Mg 浓度下分析寡核苷酸。