Cibacron Blue and proteomics: The mystery of the platoon missing in action

被引:4
作者
Di Girolamo, Francesco [1 ]
Righetti, Pier Giorgio [1 ]
D'Amato, Alfonsina [1 ]
Chung, Maxey C. M. [2 ,3 ]
机构
[1] Politecn Milan, Dept Chem Mat & Chem Engn Giulio Natta, I-20131 Milan, Italy
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Oncoprote Lab, Singapore 115597, Singapore
[3] Natl Univ Singapore, Fac Sci, Dept Biol Sci, Singapore 115597, Singapore
关键词
Combinatorial peptide ligand libraries; Dye ligand affinity chromatography; Plasma; Biomarkers; DYE-LIGAND; PLASMA-PROTEINS; CHROMATOGRAPHY; ALBUMIN; SEPARATION; MECHANISM; BINDING;
D O I
10.1016/j.jprot.2011.06.033
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The use of Cibacron Blue columns (HiTrapBlue) in proteome analysis for removal of plasma albumin, for facilitating biomarker discovery, has not borne any fruit. In fact, the visibility of low-abundance proteins was obscured. It is here reported that, upon albumin sequestering from plasma, there is adsorption, via hydrophobic interaction, of a substantial number of plasma proteins, which are lost for subsequent analysis if the blue resin is eluted via an ion shock (2 M NaCl) or with a somewhat more robust eluant (5 M urea, 2 M thiourea, 2% CHAPS, 2% sulphobetain 3-10) as recommended by manufacturers. Such treatments, in fact, release at most 25 to 30 unique gene products, including albumin. If, however, the Affigel-Blue resin, after elution with either of the two above eluants, is further eluted with boiling 4% SDS in 25 mM DTT, all the missing proteins (amounting to at least 112 unique species) are desorbed and biomarker analysis can be conducted in a correct way. It is also suggested that such blue-resin treatment could be coupled to ProteoMiner adsorption, this coupled treatment further enhancing the chances of success for discovery of low-abundance proteins. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2856 / 2865
页数:10
相关论文
共 31 条
[1]   An approach to remove albumin for the proteomic analysis of low abundance biomarkers in human serum [J].
Ahmed, N ;
Barker, G ;
Oliva, K ;
Garfin, D ;
Talmadge, K ;
Georgiou, H ;
Quinn, M ;
Rice, G .
PROTEOMICS, 2003, 3 (10) :1980-1987
[2]  
BARNEA E, 2006, EXPLORING HUMAN PLAS, P185
[3]  
Batista-Viera Francisco, 2011, Methods Biochem Anal, V54, P221
[4]   High-abundance proteins depletion for serum proteomic analysis: concomitant removal of non-targeted proteins [J].
Bellei, Elisa ;
Bergamini, Stefania ;
Monari, Emanuela ;
Fantoni, Luca Isaia ;
Cuoghi, Aurora ;
Ozben, Tomris ;
Tomasi, Aldo .
AMINO ACIDS, 2011, 40 (01) :145-156
[5]   TRIAZINE DYE BINDING OF HUMAN ALPHA-FETOPROTEIN AND ALBUMIN [J].
BIRKENMEIER, G ;
USBECK, E ;
SARO, L ;
KOPPERSCHLAGER, G .
JOURNAL OF CHROMATOGRAPHY, 1983, 265 (01) :27-35
[6]   APPLICATION OF DYE-LIGAND CHROMATOGRAPHY TO THE ISOLATION OF ALPHA-1-PROTEINASE INHIBITOR AND ALPHA-1-ACID GLYCOPROTEIN [J].
BIRKENMEIER, G ;
KOPPERSCHLAGER, G .
JOURNAL OF CHROMATOGRAPHY, 1982, 235 (01) :237-248
[7]   The art of observing rare protein species in proteomes with peptide ligand libraries [J].
Boschetti, Egisto ;
Righetti, Pier Giorgio .
PROTEOMICS, 2009, 9 (06) :1492-1510
[8]   ISOLATION OF PURE, ACTIVE ALPHA-2 MACROGLOBULIN FROM SMALL-SCALE PLASMA SAMPLES [J].
BRIDGES, MA ;
APPLEGARTH, DA ;
JOHANNSON, J ;
DAVIDSON, AGF ;
WONG, LTK .
CLINICA CHIMICA ACTA, 1982, 118 (01) :21-31
[9]   Combinatorial peptide ligand libraries for urine proteome analysis: Investigation of different elution systems [J].
Candiano, Giovanni ;
Dimuccio, Veronica ;
Bruschi, Maurizio ;
Santucci, Laura ;
Gusmano, Rosanna ;
Boschetti, Egisto ;
Righetti, Pier Giorgio ;
Ghiggeri, Gian Marco .
ELECTROPHORESIS, 2009, 30 (14) :2405-2411
[10]  
Dean P.D.G., 1985, AFFINITY CHROMATOGRA