High-throughput characterization of lipopolysaccharide-binding proteins using mass spectrometry

被引:4
|
作者
Kim, Yun-Gon [2 ]
Yang, Yung-Hun [5 ]
Kim, Byung-Gee [1 ,2 ,3 ,4 ]
机构
[1] Seoul Natl Univ, Coll Engn, Sch Chem & Biol Engn, Seoul 151742, South Korea
[2] Seoul Natl Univ, Inst Mol Biol & Genet, Seoul 151742, South Korea
[3] Seoul Natl Univ, Engn Res Inst, Seoul 151742, South Korea
[4] Seoul Natl Univ, Inst Bioengn, Seoul 151742, South Korea
[5] Konkuk Univ, Coll Engn, Dept Microbial Engn, Seoul, South Korea
关键词
Lipopolysaccharide (LPS); LPS-binding proteins; Mass spectrometry (MS); Human serum; GRAM-NEGATIVE BACTERIA; EPOXY BEADS; LPS; PEPTIDES; ENDOTOXIN; IDENTIFICATION; RECOGNITION; ACTIVATION; MECHANISMS; RECEPTORS;
D O I
10.1016/j.jchromb.2010.10.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Lipopolysaccharide (LPS)-binding proteins interact with LPS in human serum and mediate various immune responses We describe a high-throughput LPS-binding protein profiling platform for discovering unknown LPS-binding proteins and potential inflammatory mediators As a pull-down method the LPS molecules were immobilized onto epoxy beads and then directly incubated with human serum to screen LPS-binding proteins Through the "untargeted mass spectrometric approach potential LPS-binding proteins which elicit various immune responses in human serum were identified by a highly sensitive LTQ Orbitrap Hybrid Fourier Transform Mass Spectrometer (LTQ Orbitrap FT MS) Therefore this mass spectrometry (MS)-based profiling method is straightforward for screening unknown LPS-binding proteins and provides physiologically relevant binding partners in human serum (C) 2010 Elsevier B V All rights reserved
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页码:3323 / 3326
页数:4
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