Decrease of dynamic range of proteins in human plasma by ampholine immobilized polymer microspheres

被引:5
|
作者
Deng, Nan [1 ,2 ]
Zhu, Guijie [1 ]
Chen, Yuanbo [1 ,2 ]
Wu, Qi [1 ,2 ]
Liang, Zhen [1 ]
Sui, Zhigang [1 ]
Zhang, Lihua [1 ]
Yang, Kaiguang [1 ]
Zhang, Yukui [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Key Lab Separat Sci Analyt Chem, Natl Chromatog Res & Anal Ctr, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Ampholine; Fractionation; Human plasma; Protein dynamic range; MULTIDIMENSIONAL LIQUID-CHROMATOGRAPHY; LECTIN AFFINITY-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; LIGAND LIBRARY TREATMENT; HUMAN SERUM PROTEOME; EXCHANGE CHROMATOGRAPHY; BIOMARKER DISCOVERY; GEL ELECTROPHORESIS; PEPTIDE LIBRARIES; REVERSED-PHASE;
D O I
10.1016/j.aca.2014.04.004
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel protein sample pretreatment method based on ampholine immobilized polymer microsphere (ampholine@PM) was developed for the fractionation of intact proteins prior to protein digestion and peptide analysis to reduce the dynamic range of human plasma proteome. After incubation with our prepared ampholine@PM, the captured plasma proteins were successively desorbed by 2 M NaCl, 100 mM glycine-hydrochloric acid, and 30% (v/v) acetonitrile with 0.1% (v/v) trifluoroacetic acid. The SDS-PAGE results showed the protein dynamic range in such three fractions was obviously reduced as compared with the native plasma. On-particle digestion was ultimately performed to release all proteins retained on ampholine@PM. Followed by MuPIT analysis, the number of identified proteins in plasma was improved by 75% after ampholine@PM treatment. Furthermore, the spectral count of 9 high abundance proteins was decreased by 37.6-97.2%, and the identified low abundance protein (< 100 ng mL(-1)) number was increased from 4 to 17. These results demonstrated that the fractionation by ampholine@PM could efficiently decrease the protein dynamic range in abundance, beneficial to achieve the deep coverage identification of human plasma proteome. (c) 2014 Elsevier B. V. All rights reserved.
引用
收藏
页码:43 / 50
页数:8
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