Hamdan M, Curcuruto O
Glaxo Research Laboratories, Verona, Italy.
Rapid Commun Mass Spectrom. 1994 Mar;8(3):274-9. doi: 10.1002/rcm.1290080310.
Collision-induced dissociation (CID) of several protonated peptides formed by positive-ion electrospray (ES+) and by Cs+ fast-ion bombardment are reported. The CID spectra of ions formed by the first ionization method were effected at elevated extraction cone voltages within the ion source of a single quadrupole instrument, while linked-fields-scan measurements at constant B/E of ions formed by the latter technique were performed within the collision cell of a trisector instrument. For molecular masses below 1000 Da, the two sets of spectra yielded identical sequencing information; however, for higher molecular masses the similarity was less evident. This divergence between the two sets of measurements is partially attributed to dominant doubly charged ions and less efficient dissociation of sodium adduct ions at elevated cone voltages.
报道了通过正离子电喷雾(ES+)和Cs+快离子轰击形成的几种质子化肽的碰撞诱导解离(CID)。由第一种电离方法形成的离子的CID光谱是在单四极杆仪器的离子源内升高的提取锥电压下获得的,而通过后一种技术形成的离子在恒定B/E下的联动场扫描测量是在扇形场仪器的碰撞池中进行的。对于分子量低于1000 Da的情况,两组光谱产生了相同的测序信息;然而,对于更高的分子量,相似性不太明显。两组测量之间的这种差异部分归因于占主导地位的双电荷离子以及在升高的锥电压下钠加合物离子的解离效率较低。