COLLISION-INDUCED DISSOCIATION OF PEPTIDE IONS .3. COMPARISON OF RESULTS OBTAINED USING SECTOR-QUADRUPOLE HYBRIDS WITH THOSE FROM TANDEM DOUBLE-FOCUSING INSTRUMENTS

被引:67
作者
ALEXANDER, AJ
THIBAULT, P
BOYD, RK
CURTIS, JM
RINEHART, KL
机构
[1] NATL RES COUNCIL CANADA,ATLANTIC REG LAB,HALIFAX B3H 3Z1,NS,CANADA
[2] UNIV ILLINOIS,SCH CHEM SCI,URBANA,IL 61801
来源
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES | 1990年 / 98卷 / 02期
关键词
D O I
10.1016/0168-1176(90)85012-Q
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
Two series of peptides, viz., dynorphin fragments (up to 9 residues) and oligomers of phenylalanine, have been studied by collision induced dissociation (CID) of their protonated forms produced by fast atom bombardment (FAB) ionization. Spectra were obtained using both a four-sector tandem instrument (CID in the kiloelectronvolt range) and a tandem hybrid instrument (CID at a few tens of electronvolts). The four-sector instrument provided fragment spectra of excellent quality under conditions simulating a real-world analytical situation, i.e. 1-2 nmol of material available, although the FAB efficiency for Phe8, was so low (precursor ion beam current ∼ 10-14 A) that no useful fragment spectra were obtained. The hybrid instrument provided abundant fragment ions for smaller precursors (molecular weights < 500-600 Da) but for larger precursors (≥ 800 Da or so) the CID efficiency was much reduced and highly susceptible to composition effects, particularly the presence of highly basic amino acid residues. The information content of these spectra was evaluated objectively via two complementary computer algorithms. The limitations of CID in r.f.-only quadrupole collision cells are not due primarily to ion transmission effects, since examples of good quality spectra for large precursors are presented. The low efficiency of collisional activation of organic ions of m/z ≥ 800 Da or so, under conditions typical of quadrupole collision cells, was confirmed by the observation that in those cases where abundant fragment ions were obtained the corresponding spectra obtained in absence of collision gas were of comparable quality. The differences between collisional activation of such ions in the kiloelectronvolt range and in the electronvolt range, as well as the dramatic differences between low energy CID of large and small precursor ions, are discussed in terms of fundamental considerations of inelastic collisions. Finally, the qualitatively different kinds of fragmentation reactions, observed in the two regimes of collision energy, are described. In both cases the well-known peptide sequence fragments were observed. The high-energy CID also produced intense fragments arising from cleavage of all or part of sidechains (d, s, v and w series) which were entirely absent from the low-energy spectra. The latter contained abundant internal cleavage ions (both N- and C-terminus residues lost) which were relatively weak in the high-energy spectra. Loss of the C-terminus residue was observed in both regimes as a low-energy process in the absence of collision gas, although the compositional conditions giving rise to this process have not been determined in the present work. © 1990.
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页码:107 / 134
页数:28
相关论文
共 75 条
[1]   EXPERIMENTAL INVESTIGATIONS OF FACTORS CONTROLLING THE COLLISION-INDUCED DISSOCIATION SPECTRA OF PEPTIDE IONS IN A TANDEM HYBRID MASS-SPECTROMETER .1. LEUCINE ENKEPHALIN [J].
ALEXANDER, AJ ;
BOYD, RK .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1989, 90 (03) :211-240
[2]  
Alexander AJ, 1989, RAPID COMMUN MASS SP, V3, P364
[3]  
ALEXANDER AJ, 1988, RAPID COMMUN MASS SP, V2, P30
[4]  
ASHCROFT AE, 1988, 36TH ANN C MASS SPEC, P1156
[5]   CHARGE INVERSION SPECTRA OF THE [M-H]- IONS OF DIPEPTIDES AND POLYPEPTIDES ANALYZED BY FAST-ATOM-BOMBARDMENT MASS-SPECTROMETRY [J].
BERTRAND, MJ ;
THIBAULT, P .
BIOMEDICAL AND ENVIRONMENTAL MASS SPECTROMETRY, 1986, 13 (07) :347-355
[6]  
Beynon JH, 1986, ADV MASS SPECTROM, V10, P437
[7]   CONTRIBUTIONS OF MASS-SPECTROMETRY TO PEPTIDE AND PROTEIN-STRUCTURE [J].
BIEMANN, K .
BIOMEDICAL AND ENVIRONMENTAL MASS SPECTROMETRY, 1988, 16 (1-12) :99-111
[8]   VIBRATIONAL-EXCITATION IN H+ (D+)-CO2 COLLISIONS - MODE SELECTIVITY AND TIME EFFECTS [J].
BISCHOF, G ;
HERMANN, V ;
KRUTEIN, J ;
LINDER, F .
JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS, 1982, 15 (02) :249-261
[9]   A PRACTICAL APPROACH TO LINKED E-Q SCANS OVER A WIDE MASS RANGE - PARTIALLY LINKED SCANS WITH E-MODULATION [J].
BOYD, RK ;
DYER, EW ;
GUEVREMONT, R .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1989, 88 (2-3) :147-160
[10]   ION CURRENT SURFACES FOR A TANDEM DOUBLE-FOCUSSING MASS-SPECTROMETER WITH A FLOATABLE GAS COLLISION CELL [J].
BOYD, RK ;
HARVAN, DJ ;
HASS, JR .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1985, 65 (03) :273-286