Comparison of Different Signal Thresholds on Data Dependent Sampling in Orbitrap and LTQ Mass Spectrometry for the Identification of Peptides and Proteins in Complex Mixtures

被引:38
作者
Wong, Catherine C. L. [1 ]
Cociorva, Daniel [1 ]
Venable, John D. [1 ]
Xu, Tao [1 ]
Yates, John R., III [1 ]
机构
[1] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
关键词
SPECTRA; MS/MS;
D O I
10.1016/j.jasms.2009.04.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We evaluate the effect of ion-abundance threshold settings for data-dependent acquisition on a hybrid LTQ-Orbitrap mass spectrometer, analyzing features Such as the total number of spectra collected, the signal to noise ratio of the full MS scans, the spectral quality of the tandem mass spectra acquired, and the number of peptides and proteins identified from a complex mixture. We find that increasing the threshold for data-dependent acquisition generally decreases the quantity but increases the quality of the spectra acquired. This is especially true when the threshold setting is set above the noise level of the full MS scan. We compare two distinct experimental configurations: one where full MS scans are acquired in the Orbitrap analyzer while tandem MS scans are acquired in the LTQ analyzer, and one where both full MS and tandem MS scans are acquired in the LTQ analyzer. We examine the number of spectra, peptides, and proteins identified under various threshold conditions, and we find that the optimal threshold setting is at or below the respective noise level of the instrument regardless of whether the full MS scan is performed in the Orbitrap or in the LTQ analyzer. When comparing the high-throughput identification performance of the two analyzers, we conclude that, used at optimal threshold levels, the LTQ and the Orbitrap identify similar numbers of peptides and proteins. The higher scan speed of the LTQ, which results in more spectra being collected, is roughly compensated by the higher mass accuracy of the Orbitrap, which results in improved database searching and peptide validation software performance. (J Am Soc Mass Spectrom 2009, 20, 1405-1414) (C) 2009 Published by Elsevier Inc. on behalf of American Society for Mass Spectrometry
引用
收藏
页码:1405 / 1414
页数:10
相关论文
共 15 条
[1]   Automatic Quality Assessment of Peptide Tandem Mass Spectra [J].
Bern, Marshall ;
Goldberg, David ;
McDonald, W. Hayes ;
Yates, John R., III .
BIOINFORMATICS, 2004, 20 :49-54
[2]  
Cociorva Daniel, 2007, Curr Protoc Bioinformatics, VChapter 13, DOI 10.1002/0471250953.bi1304s16
[3]   AN APPROACH TO CORRELATE TANDEM MASS-SPECTRAL DATA OF PEPTIDES WITH AMINO-ACID-SEQUENCES IN A PROTEIN DATABASE [J].
ENG, JK ;
MCCORMACK, AL ;
YATES, JR .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (11) :976-989
[4]   Direct analysis of protein complexes using mass spectrometry [J].
Link, AJ ;
Eng, J ;
Schieltz, DM ;
Carmack, E ;
Mize, GJ ;
Morris, DR ;
Garvik, BM ;
Yates, JR .
NATURE BIOTECHNOLOGY, 1999, 17 (07) :676-682
[5]   A correlation algorithm for the automated quantitative analysis of shotgun proteomics data [J].
MacCoss, MJ ;
Wu, CC ;
Liu, HB ;
Sadygov, R ;
Yates, JR .
ANALYTICAL CHEMISTRY, 2003, 75 (24) :6912-6921
[6]   INTERPRETING MASS-SPECTRA OF MULTIPLY CHARGED IONS [J].
MANN, M ;
MENG, CK ;
FENN, JB .
ANALYTICAL CHEMISTRY, 1989, 61 (15) :1702-1708
[7]   MS1, MS2, and SQT - three unified, compact, and easily parsed file formats for the storage of shotgun proteomic spectra and identifications [J].
McDonald, WH ;
Tabb, DL ;
Sadygov, RG ;
MacCoss, MJ ;
Venable, J ;
Graumann, J ;
Johnson, JR ;
Cociorva, D ;
Yates, JR .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2004, 18 (18) :2162-2168
[8]   Comparison of three directly coupled HPLC MS/MS strategies for identification of proteins from complex mixtures: single-dimension LC-MS/MS, 2-phase MudPIT, and 3-phase MudPIT [J].
McDonald, WH ;
Ohi, R ;
Miyamoto, DT ;
Mitchison, TJ ;
Yates, JR .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2002, 219 (01) :245-251
[9]   Evaluation of multidimensional chromatography coupled with tandem mass spectrometry (LC/LC-MS/MS) for large-scale protein analysis: The yeast proteome [J].
Peng, JM ;
Elias, JE ;
Thoreen, CC ;
Licklider, LJ ;
Gygi, SP .
JOURNAL OF PROTEOME RESEARCH, 2003, 2 (01) :43-50
[10]   Data-controlled automation of liquid chromatography tandem mass spectrometry analysis of peptide mixtures [J].
Stahl, DC ;
Swiderek, KM ;
Davis, MT ;
Lee, TD .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1996, 7 (06) :532-540