Proteomic investigation of natural killer cell microsomes using gas-phase fractionation by mass spectrometry

被引:22
作者
Blonder, J
Rodriguez-Galan, MC
Lucas, DA
Young, HA
Issaq, HJ
Veenstra, TD
Conrads, TP
机构
[1] NCI, SAIC Frederick Inc, Lab Proteom & Analyt Technol, Biomed Proteom Program, Frederick, MD 21702 USA
[2] NCI, Expt Immunol Lab, Frederick, MD 21702 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2004年 / 1698卷 / 01期
关键词
gas-phase fractionation; mass spectrometry; natural killer cell; membrane proteomic; microsome;
D O I
10.1016/j.bbapap.2003.10.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have explored the utility of gas-phase fractionation by mass spectrometry (MS) in the mass-to-charge (m/z) dimension (GPF(m/z)) for increasing the effective number of protein identifications in cases where sample quantity limits the use of multi-dimensional chromatographic fractionation. A peptide digestate from proteins isolated from the membrane fraction of natural killer (NK) cells was analyzed by microcapillary reversed-phase liquid chromatography coupled online to an ion-trap (IT) mass spectrometer. Performing GPF(m/z). using eight narrow precursor ion scan m1z ranges enabled the identification of 340 NK cell proteins from 12 mug of digestate, representing more than a fivefold increase in the number of proteins identified as compared to the same experiment employing a standard precursor ion survey scan m/z range (i.e., m/z 400-2000). The results show that GPF(m/z) represents an effective technique for increasing protein identifications in global proteomic investigations especially when sample quantity is limited. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 95
页数:9
相关论文
共 14 条
[1]  
Davis MT, 2001, PROTEOMICS, V1, P108, DOI 10.1002/1615-9861(200101)1:1<108::AID-PROT108>3.0.CO
[2]  
2-5
[3]   Laser capture microdissection [J].
EmmertBuck, MR ;
Bonner, RF ;
Smith, PD ;
Chuaqui, RF ;
Zhuang, ZP ;
Goldstein, SR ;
Weiss, RA ;
Liotta, LA .
SCIENCE, 1996, 274 (5289) :998-1001
[4]   A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice [J].
Fleming, MD ;
Campagna, DR ;
Haslett, JN ;
Trenor, CC ;
Andrews, NC .
GENES & DEVELOPMENT, 2001, 15 (06) :652-657
[5]  
Fogler WE, 1996, J IMMUNOL, V156, P4707
[6]   Direct analysis and identification of proteins in mixtures by LC/MS/MS and database searching at the low-femtomole level [J].
McCormack, AL ;
Schieltz, DM ;
Goode, B ;
Yang, S ;
Barnes, G ;
Drubin, D ;
Yates, JR .
ANALYTICAL CHEMISTRY, 1997, 69 (04) :767-776
[7]  
Ortaldo JR, 1999, J IMMUNOL, V163, P5269
[8]   Linking genome and proteome by mass spectrometry: Large-scale identification of yeast proteins from two dimensional gels [J].
Shevchenko, A ;
Jensen, ON ;
Podtelejnikov, AV ;
Sagliocco, F ;
Wilm, M ;
Vorm, O ;
Mortensen, P ;
Shevchenko, A ;
Boucherie, H ;
Mann, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14440-14445
[9]   Large-scale analysis of the yeast proteome by multidimensional protein identification technology [J].
Washburn, MP ;
Wolters, D ;
Yates, JR .
NATURE BIOTECHNOLOGY, 2001, 19 (03) :242-247
[10]   Femtomole sequencing of proteins from polyacrylamide gels by nano-electrospray mass spectrometry [J].
Wilm, M ;
Shevchenko, A ;
Houthaeve, T ;
Breit, S ;
Schweigerer, L ;
Fotsis, T ;
Mann, M .
NATURE, 1996, 379 (6564) :466-469