Fournier I, Brunot A, Tabet J C, Bolbach G
Université Pierre et Marie Curie, Laboratoire de Chimie Structurale Organique et Biologique, CNRS-UMR 7613, Boîte 45, 4 Place Jussieu, 75252 Paris Cedex 05, France.
J Mass Spectrom. 2005 Jan;40(1):50-9. doi: 10.1002/jms.772.
Delayed extraction experiments were undertaken to gain a better insight into the dynamic effects involved in the ion formation in UV matrix-assisted laser desorption/ionization. Part I1 was devoted to a 2,5-dihydroxybenzoic (2,5-DHB) matrix. The results clearly demonstrated the existence and the role of high-mass precursors corresponding to a non-covalent matrix-analyte association in ion formation. In this complementary study, ion flight time and abundance were studied as a function of the delay extraction time using the matrix alpha-cyano-4-hydroxycinnamic acid (HCCA). Under our instrumental conditions, where ejected ions experienced a low repulsing electric field before extraction, two main results were obtained: (i) two ion components are observed in the peak profiles depending on the repulsing field, a first, major component (I) similar to that observed for 2,5-DHB and a second, minor component (II) apparently triggered by the delayed extraction pulse, and (ii) ion time-of-flight variation vs delay time remained lower than that noted with 2,5-DHB matrix, indicating that the initial axial velocity is smaller. The initial kinetic energy of matrix and low molecular mass peptide ions for the component I is not high enough to overcome the repulsing potential in the delay time range (200-2200 ns) and we have to assume that ions have non-covalent clusters as precursors. Complete desolvation of these clusters-aggregates would be achieved through the extraction step. Simulations of the ion time-of-flight as a function of the delay time allow the determination of the average size of the precursors, typically 4500, 40000 and 50000 u for HCCA, ACTH 7-38 and bovine insulin quasi-molecular ion, respectively, assuming that the precursors are singly charged. The size of these ion precursors is greater than that of those generated for 2,5-DHB. For component II, ions are probably not solvated and they are directly desorbed from the target. Taking into account the results on HCCA and 2,5-DHB matrices and other results from the literature, a general model for ion formation based on clusters as ion precursors is proposed and discussed.
进行了延迟提取实验,以更深入地了解紫外基质辅助激光解吸/电离中离子形成所涉及的动态效应。第二部分专门研究了2,5-二羟基苯甲酸(2,5-DHB)基质。结果清楚地证明了在离子形成过程中,对应于非共价基质-分析物缔合的高质量前体的存在及其作用。在这项补充研究中,使用α-氰基-4-羟基肉桂酸(HCCA)基质,研究了离子飞行时间和丰度与延迟提取时间的关系。在我们的仪器条件下,即喷射出的离子在提取前经历低排斥电场,得到了两个主要结果:(i)根据排斥场的不同,在峰形中观察到两个离子组分,第一个主要组分(I)与2,5-DHB中观察到的类似,第二个次要组分(II)显然由延迟提取脉冲触发;(ii)离子飞行时间随延迟时间的变化仍低于2,5-DHB基质,表明初始轴向速度较小。组分I的基质和低分子量肽离子的初始动能不足以克服延迟时间范围(200-2200 ns)内的排斥势,我们不得不假设离子以非共价簇作为前体。这些簇聚集体的完全去溶剂化将通过提取步骤实现。作为延迟时间函数的离子飞行时间模拟允许确定前体的平均大小,假设前体为单电荷,对于HCCA、促肾上腺皮质激素7-38和牛胰岛素准分子离子,其平均大小通常分别为4500、40000和50000 u。这些离子前体的大小大于2,5-DHB产生的前体。对于组分II,离子可能没有溶剂化,它们直接从靶上解吸。考虑到HCCA和2,5-DHB基质的结果以及文献中的其他结果,提出并讨论了基于簇作为离子前体的离子形成通用模型。