Use of non-porous reversed-phase high-performance liquid chromatography for protein profiling and isolation of proteins induced by temperature variations for Siberian permafrost bacteria with identification by matrix-assisted laser desorption lionization time-of-flight mass spectrometry and capillary electrophoresis-electrospray ionization mass spectrometry

被引:24
作者
Chong, BE
Kim, J
Lubman, DM
Tiedje, JM
Kathariou, S
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[2] Michigan State Univ, Ctr Microbial Ecol, E Lansing, MI 48824 USA
[3] Univ Hawaii Manoa, Dept Microbiol, Honolulu, HI 96822 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2000年 / 748卷 / 01期
关键词
proteins;
D O I
10.1016/S0378-4347(00)00288-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Non-porous reversed-phase high-performance liquid chromatography (NP-RP-HPLC) has been used to separate and isolate proteins from whole cell lysates of ED 7-3, a bacterium from the buried Siberian permafrost sediment. The proteins collected from the liquid eluent of this separation were then analyzed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) and capillary electrophoresis-electrospray ionization mass spectrometry (CE-ESI-MS). In order to study the differences in expression of cold-shock proteins (CSPs) at different growth temperatures, cultures of the ED 7-3 strain were prepared at 4 degreesC and 25 degreesC. The goals of this work were twofold: firstly, to identify the presence of CSPs and other proteins that are highly expressed at 4 degreesC but not at 25 degreesC; and secondly, to isolate these proteins for MALDI-TOF-MS and CE-ESI-MS identification. In this initial work, distinct protein profiles were observed for these cultures as a function of temperature. Fraction collection from the eluent of NP-RP-HPLC of some of the highly expressed proteins was performed and the proteins were mass analyzed for molecular mass. Peptide maps of the proteins were generated by tryptic digestion and were analyzed by CE-ESI-MS and MALDI-TOF-MS for database identification of the expressed proteins. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:167 / 177
页数:11
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