In-Source Decay and Pseudo-MS3 of Peptide and Protein Ions Using Liquid AP-MALDI

被引:12
作者
Ait-Belkacem, Rima [1 ]
Dilillo, Marialaura [1 ,2 ]
Pellegrini, Davide [1 ,3 ]
Yadav, Avinash [1 ]
de Graaf, Erik L. [1 ]
McDonnell, Liam A. [1 ,4 ]
机构
[1] Fdn Pisana Sci ONLUS, Pisa, Italy
[2] Univ Pisa, Dipartimento Chim & Chim Ind, Pisa, Italy
[3] Scuola Normale Super Pisa, Pisa, Italy
[4] Leiden Univ, Dept Pathol, Med Ctr, Leiden, Netherlands
关键词
MALDI; In-source decay; MS/MS; Pseudo MS3; T3; sequencing; ASSISTED-LASER-DESORPTION/IONIZATION; FLIGHT-MASS-SPECTROMETRY; SEQUENCE INFORMATION; SOURCE FRAGMENTATION; MATRICES; DESORPTION; TIME; PHOSPHOLIPIDS; IONIZATION; MS;
D O I
10.1007/s13361-016-1511-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Atmospheric pressure MALDI on a Q-Exactive instrument was optimized for in-source decay and pseudo-MS3. The dependence of AP-MALDI ISD on the MALDI liquid matrix was investigated for peptides and proteins. The liquid matrices enabled long-life ISD signal, and exhibited high fragment ion yield and signal stability. Extensive a-, b-, c-, y-, and z-type fragment series were observed depending on the matrix used but were most extensive with 2,5-DHB. Complete sequence coverage of small peptide and intact protein-terminus sequence tags were obtained and confirmed using HCD as a pseudo-MS3 method.
引用
收藏
页码:2075 / 2079
页数:5
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