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
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