Serine–phosphoric acid cluster ions studied by electrospray ionization and tandem mass spectrometry

✍ Scribed by Xianglei Kong

• Book ID: 102905340
• Publisher: John Wiley and Sons
• Year: 2011
• Tongue: English
• Weight: 656 KB
• Volume: 46
• Category: Article
• ISSN: 1076-5174
• DOI: 10.1002/jms.1922

✦ Synopsis

Abstract

More than 310 kinds of cluster ions of S~m~P~n~H~k~^k+^ are observed in a single ESI mass spectrum of a mixed solution of serine and phosphoric acid. Some typical cluster ions are selected, activated by collision in a FT ICR cell, and the dissociation pathways were deduced in detail. For large singly protonated ions, the collisions cause the ejection of subunits of serine or phosphoric acid subsequently producing the ions of S~2~P~4~H~1~^1+^, which can be further dissociated by the loss of phosphoric acid molecules in turn and form the protonated serine dimer and monomer. However, for the doubly protonated ions, the dissociation pathways change from the loss of a protonated serine dimer for the ions of S~7~P~9~H~2~^2+^ to the neutral loss of H~3~PO~4~ for the ions of S~7~P~12~H~2~^2+^ or the neutral loss of serine or H~3~PO~4~ for the larger clusters, indicating the effect of cluster sizes on the process of dissociation. The structure of S~2~P~4~H~1~^1+^ is suggested based on B3LYP/6‐31G(d,p) calculations. The diversity and structural orderliness of the hetero‐cluster ions are mainly attributed to the network of hydrogen bonds inside the cluster ions and the extraordinary amphotericity of the components. Copyright © 2011 John Wiley & Sons, Ltd.