New Insights into the Vacuum UV Photodissociation of Peptides

被引:42
作者
Parthasarathi, Ramakrishnan [1 ]
He, Yi [1 ]
Reilly, James P. [1 ]
Raghavachari, Krishnan [1 ]
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
基金
美国国家科学基金会;
关键词
SURFACE-INDUCED DISSOCIATION; MAIN FRAGMENTATION PATHWAYS; SINGLY PROTONATED PEPTIDES; ELECTRON DETACHMENT DISSOCIATION; CHARGE-REMOTE FRAGMENTATIONS; FLIGHT MASS-SPECTROMETER; 193; NM; RYDBERG STATES; ULTRAVIOLET PHOTOFRAGMENTATION; ACTIVATED DISSOCIATION;
D O I
10.1021/ja907975v
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Vacuum ultraviolet laser photodissociation (UVPD) of peptide ions leads to unusual dissociation channels involving backbone C-C bond breaking. However, the molecular basis for the observed behavior is not clearly understood. We now report theoretical investigations using ab initio/density functional theory (DFT) techniques on neutral and protonated dipeptides undergoing vacuum ultraviolet (VUV) induced fragmentation via a Rydberg excitation (and/or electron detachment) and subsequent C-C bond cleavage. New experimental results on VUV photodissociation of dipeptides (protonated Ala_Arg and Arg_Ala) provide strong support for our proposed model. Our mechanism also provides a natural explanation for the presence of immonium ions that are sometimes observed in such experiments.
引用
收藏
页码:1606 / 1610
页数:5
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