Xia Yu, Liang Xiaorong, McLuckey Scott A
Department of Chemistry, Purdue University, West Lafayette, Indiana 47907-2084, USA.
Anal Chem. 2005 Jun 1;77(11):3683-9. doi: 10.1021/ac0481811.
A single sonic spray source has been used to generate both positive and negative ions for subsequent ion/ion reaction experiments. Ion/ion reactions took place after ions of each polarity were sequentially injected into a linear ion trap, where axial trapping was effected by applying an auxiliary radio frequency voltage to one end lens. Absolute charge reductions via proton transfer were demonstrated for multiply charged protein/peptide cations and multiply charged oligonucleotide anions. Deprotonation of polypeptide cations occurs with anions derived from fluorinated compounds such as nonadecafluoro-1-decanol and perfluoro-1-octanol, while multiply charged oligonucleotide anions are efficiently protonated via reaction with proton sponge (N,N,N',N'-tetramethyl-1,8-naphthalenediamine) cations. No evidence for signal suppression of the biopolymer ions was noted to result from the presence of these reagents in the solution subjected to sonic spray. Several of the analytically useful applications of ion/ion proton-transfer reactions are demonstrated using a single sonic spray ion source. These include an ion parking experiment for the purpose of gas-phase ion concentration and charge-state reduction of product ions formed via beam-type and in-trap collision-induced dissociation of multiply charged oligonucleotide parent anions. Examples of complex formation are also given to illustrate the flexibility of the sonic spray-induced ion/ion reaction method.
单个声波喷雾源已被用于产生正离子和负离子,以进行后续的离子/离子反应实验。在将每种极性的离子依次注入线性离子阱后发生离子/离子反应,在该离子阱中,通过向一端透镜施加辅助射频电压来实现轴向捕获。对于多电荷蛋白质/肽阳离子和多电荷寡核苷酸阴离子,通过质子转移实现了绝对电荷减少。多肽阳离子的去质子化与来自氟化化合物(如十九氟-1-癸醇和全氟-1-辛醇)的阴离子发生,而多电荷寡核苷酸阴离子通过与质子海绵(N,N,N',N'-四甲基-1,8-萘二胺)阳离子反应有效地质子化。在进行声波喷雾的溶液中存在这些试剂,未发现生物聚合物离子信号抑制的证据。使用单个声波喷雾离子源展示了离子/离子质子转移反应的几个分析上有用的应用。这些应用包括用于气相离子浓缩和通过多电荷寡核苷酸母阴离子的束型和阱内碰撞诱导解离形成的产物离子的电荷态降低的离子停放实验。还给出了络合物形成的例子,以说明声波喷雾诱导的离子/离子反应方法的灵活性。