James Patrick F, Perugini Matthew A, O'Hair Richard A J
Eur J Mass Spectrom (Chichester). 2007;13(6):433-6. doi: 10.1255/ejms.897.
The collision induced dissociation (CID) spectra of the divalent metal complexes of 1-palmitoyl-2-oleoyl-sn- glycero-3-phosphocholine, Metal(lI)(L)(2) (where metal = Cu(2+), Mg(2+) and Ca(2+), L = [16:0/18:1GPCho]), formed by electrospray ionization, reveal interesting metal dependant fragmentation chemistry. Six main classes of reaction are observed corresponding to: two competing carboxylate abstraction pathways (from the sn1 and sn2 positions); phosphate abstraction; competing losses of the two different carboxylic acids from the sn1 and sn2 positions; loss of a protonated ligand, L + H. The relative ratios of the competing carboxylate abstraction reactions are dependant on the metal, with the Cu and Ca complexes favouring the abstraction of the larger carboxylate (18:1) and the Mg complex favoring the abstraction of the smaller carboxylate (16:0).
通过电喷雾电离形成的1-棕榈酰-2-油酰基-sn-甘油-3-磷酸胆碱的二价金属配合物金属(II)(L)(2)(其中金属 = Cu(2+)、Mg(2+)和Ca(2+),L = [16:0/18:1GPCho])的碰撞诱导解离(CID)光谱揭示了有趣的金属依赖性碎片化化学。观察到六种主要反应类型,分别对应:两条相互竞争的羧酸根离子夺取途径(来自sn1和sn2位置);磷酸根离子夺取;来自sn1和sn2位置的两种不同羧酸的竞争性损失;质子化配体L + H的损失。相互竞争的羧酸根离子夺取反应的相对比例取决于金属,Cu和Ca配合物有利于夺取较大的羧酸根(18:1),而Mg配合物有利于夺取较小的羧酸根(16:0)。