Preliminary comparison of precursor scans and liquid chromatography-tandem mass spectrometry on a hybrid quadrupole time-of-flight mass spectrometer

被引:58
作者
Borchers, C [1 ]
Parker, CE [1 ]
Deterding, LJ [1 ]
Tomer, KB [1 ]
机构
[1] NIEHS, Struct Biol Lab, NIH, Res Triangle Pk, NC 27709 USA
关键词
mass spectrometry; peptides; substance P; HIV-p24;
D O I
10.1016/S0021-9673(99)00479-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent mass spectrometry instrumentation developments include the appearance of novel hybrid tandem instrumentation, Q-TOF, consisting of a quadrupole mass analyzer (MS1) and a time-of-flight (TOF) analyzer. The TOF analyzer is not scanned, but collects all fragment ions entering the analyzer at a given time. Thus, the typical precursor scan experiment cannot be performed. Instead, a full MS-MS spectrum can be acquired for each mass passed by MS1. Appropriate data manipulation, i.e. extracted ion current chromatograms, can correlate specific fragment ion formation to the parent ion. Precursor scanning and LC-MS-MS are compared on a Q-TOF instrument for the determination of protein modifications, including acetylation and phosphorylation. Model peptides used for phosphopeptide detection were generated from a mixture of p-casein. Model acetylated peptides were generated from a mixture of acetylated substance P1-9 and substance P1-11. The results were then applied to a more complex mixture, a digest of HIV-p24. Results indicate that precursor scanning is useful for screening, but that LC-MS-MS has a sensitivity advantage and is less susceptible to suppression effects. LC-MS-MS, therefore, appears to be better for the detection of trace components in complex mixtures. (C) 1999 Elsevier Science BN. All rights reserved.
引用
收藏
页码:119 / 130
页数:12
相关论文
共 14 条
[1]  
BATEMAN R, 1998, P 46 ASMS C MASS SPE, P42
[2]  
CARR SA, 1993, PROTEIN SCI, V2, P183
[3]  
CARR SA, 1993, ANAL BIOCHEM, V239, P183
[4]   COAXIAL CONTINUOUS-FLOW FAST ATOM BOMBARDMENT IN CONJUNCTION WITH TANDEM MASS-SPECTROMETRY FOR THE ANALYSIS OF BIOMOLECULES [J].
DETERDING, LJ ;
MOSELEY, MA ;
TOMER, KB ;
JORGENSON, JW .
ANALYTICAL CHEMISTRY, 1989, 61 (22) :2504-2511
[5]   IDENTIFICATION OF PHOSPHORYLATED PEPTIDES FROM COMPLEX-MIXTURES USING NEGATIVE-ION ORIFICE-POTENTIAL STEPPING AND CAPILLARY LIQUID-CHROMATOGRAPHY ELECTROSPRAY-IONIZATION MASS-SPECTROMETRY [J].
DING, JM ;
BURKHART, W ;
KASSEL, DB .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1994, 8 (01) :94-98
[6]   MOLECULAR CHARACTERIZATION OF SURFACE-TOPOLOGY IN PROTEIN TERTIARY STRUCTURES BY AMINO-ACYLATION AND MASS-SPECTROMETRIC PEPTIDE-MAPPING [J].
GLOCKER, MO ;
BORCHERS, C ;
FIEDLER, W ;
SUCKAU, D ;
PRZYBYLSKI, M .
BIOCONJUGATE CHEMISTRY, 1994, 5 (06) :583-590
[7]   SELECTIVE DETECTION OF PHOSPHOPEPTIDES IN COMPLEX-MIXTURES BY ELECTROSPRAY LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY [J].
HUDDLESTON, MJ ;
ANNAN, RS ;
BEAN, MF ;
CARR, SA .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1993, 4 (09) :710-717
[8]   COLLISIONAL FRAGMENTATION OF GLYCOPEPTIDES BY ELECTROSPRAY IONIZATION LC MS AND LC MS MS - METHODS FOR SELECTIVE DETECTION OF GLYCOPEPTIDES IN PROTEIN DIGESTS [J].
HUDDLESTON, MJ ;
BEAN, MF ;
CARR, SA .
ANALYTICAL CHEMISTRY, 1993, 65 (07) :877-884
[9]  
McLuckey, 1988, MASS SPECTROMETRY MA
[10]  
Morris HR, 1996, RAPID COMMUN MASS SP, V10, P889, DOI 10.1002/(SICI)1097-0231(19960610)10:8<889::AID-RCM615>3.3.CO