Collision-induced dissociation of peptide thioesters:: the influence of peptide length on fragmentation

被引:2
作者
Buré, C
Boujard, O
Bertrand, M
Lange, C
Delmas, AF
机构
[1] CNRS, UPR 4301, Ctr Biophys Mol, F-45071 Orleans, France
[2] Univ Rouen, CNRS, UMR 6014, Spectromet Masse Bioorg, F-76821 Mont St Aignan, France
关键词
peptide thioesters; fragmentation; peptide length;
D O I
10.1255/ejms.709
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Five peptide thioesters of increasing length were fragmented using two processes, in-source and in-collision cell fragmentation, using an electrospray source coupled to a triple quadrupole mass spectrometer. Comparison of their fragmentations was made in regard to their length. The two fragmentation conditions show that the peptide length has no influence on structural information and that the fragmentation efficiency is higher for the smallest peptides than for the longest. The particularity of these peptide thioesters consists of the neutral loss of ethanethiol. The absence of the a(3) fragment ion and the presence of the (a(3)-17) ion on the collision-induced dissociation mass spectra are noted.
引用
收藏
页码:31 / 34
页数:4
相关论文
共 19 条
[1]  
Bertrand M., 2001, GEOCHEMISTRY ORIGIN, P51
[2]   CONTRIBUTIONS OF MASS-SPECTROMETRY TO PEPTIDE AND PROTEIN-STRUCTURE [J].
BIEMANN, K .
BIOMEDICAL AND ENVIRONMENTAL MASS SPECTROMETRY, 1988, 16 (1-12) :99-111
[3]   Fragmentation study of peptide acetals and aldehydes using in-source collision-induced dissociation [J].
Buré, C ;
Le Falher, G ;
Lange, C ;
Delmas, A .
JOURNAL OF MASS SPECTROMETRY, 2004, 39 (07) :817-823
[4]   Comparison of dissociation of ions in an electrospray source, or a collision cell in tandem mass spectrometry [J].
Buré, C ;
Lange, C .
CURRENT ORGANIC CHEMISTRY, 2003, 7 (15) :1613-1624
[5]   In-source fragmentation of peptide aldehydes and acetals:: influence of peptide length and charge state [J].
Buré, C ;
Gobert, W ;
Lelièvre, D ;
Delmas, A .
JOURNAL OF MASS SPECTROMETRY, 2001, 36 (10) :1149-1155
[6]   Role of the site of protonation in the low-energy decompositions of gas-phase peptide ions [J].
Cox, KA ;
Gaskell, SJ ;
Morris, M ;
Whiting, A .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1996, 7 (06) :522-531
[7]   Influence of peptide composition, gas-phase basicity, and chemical modification on fragmentation efficiency: Evidence for the mobile proton model [J].
Dongre, AR ;
Jones, JL ;
Somogyi, A ;
Wysocki, VH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (35) :8365-8374
[8]  
Harrison AG, 1999, RAPID COMMUN MASS SP, V13, P1663, DOI 10.1002/(SICI)1097-0231(19990830)13:16<1663::AID-RCM695>3.3.CO
[9]  
2-K
[10]   SEQUENCE DEPENDENCE OF PEPTIDE FRAGMENTATION EFFICIENCY CURVES DETERMINED BY ELECTROSPRAY-IONIZATION SURFACE-INDUCED DISSOCIATION MASS-SPECTROMETRY [J].
JONES, JL ;
DONGRE, AR ;
SOMOGYI, A ;
WYSOCKI, VH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1994, 116 (18) :8368-8369