Protein Equalizer™ Technology:: The quest for a "democratic proteome"

被引:180
作者
Righetti, Pier Giorgio
Boschetti, Egisto
Lomas, Lee
Citterio, Attilio
机构
[1] Politecn Milan, Dept Chem Mat & Chem Engn Giulio Natta, I-20131 Milan, Italy
[2] Ciphergen Biosyst Inc, Fremont, CA USA
关键词
combinatorial libraries; hexapeptide baits; hidden proteome; pasma proteins; urinary proteins;
D O I
10.1002/pmic.200500904
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
No proteome can be considered "democratic", but rather "oligarchic", since a few proteins dominate the landscape and often obliterate the signal of the rare ones. This is the reason why most scientists lament that, in proteome analysis, the same set of abundant proteins is seen again and again. A host of pre-fractionation techniques have been described, but all of them, one way or another, are besieged by problems, in that they are based on a "depletion principle", i.e. getting rid of the unwanted species. Yet "democracy" calls not for killing the enemy, but for giving "equal rights" to all people. One way to achieve that would be the use of "Protein Equalizer Technology" for reducing protein concentration differences. This comprises a diverse library of combinatorial ligands coupled to spherical porous beads. When these beads come into contact with complex proteomes (e.g. human urine and serum, egg white, and any cell lysate, for that matter) of widely differing protein composition and relative abundances, they are able to "equalize" the protein population, by sharply reducing the concentration of the most abundant components, while simultaneously enhancing the concentration of the most dilute species. It is felt that this novel method could offer a strong step forward in bringing the "unseen proteome" (due to either low abundance and/or presence of interference) within the detection capabilities of current proteomics detection methods. Examples are given of equalization of human urine and serum samples, resulting in the discovery of a host of proteins never reported before. Additionally, these beads can be used to remove host cell proteins from purified recombinant proteins or protein purified from natural sources that are intended for human consumption. These proteins typically reach purities of the order of 98%: higher purities often become prohibitively expensive. Yet, if incubated with "equalizer beads", these last impurities can be effectively removed at a small cost and with minute losses of the main, valuable product.
引用
收藏
页码:3980 / 3992
页数:13
相关论文
共 67 条
[1]   Purification of a D-hydantoinase using a laboratory-scale Streamline phenyl column as the initial step [J].
Abendroth, J ;
Chatterjee, S ;
Schomburg, D .
JOURNAL OF CHROMATOGRAPHY B, 2000, 737 (1-2) :187-194
[2]   The human plasma proteome - History, character, and diagnostic prospects [J].
Anderson, NL ;
Anderson, NG .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (11) :845-867
[3]   The human plasma proteome - A nonredundant list developed by combination of four separate sources [J].
Anderson, NL ;
Polanski, M ;
Pieper, R ;
Gatlin, T ;
Tirumalai, RS ;
Conrads, TP ;
Veenstra, TD ;
Adkins, JN ;
Pounds, JG ;
Fagan, R ;
Lobley, A .
MOLECULAR & CELLULAR PROTEOMICS, 2004, 3 (04) :311-326
[4]   Two-step purification method of vitellogenin from three teleost fish species:: rainbow trout (Oncorhynchus mykiss), gudgeon (Gobio gobio) and chub (Leuciscus cephalus) [J].
Brion, F ;
Rogerieux, F ;
Noury, P ;
Migeon, B ;
Flammarion, P ;
Thybaud, E ;
Porcher, JM .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2000, 737 (1-2) :3-12
[5]   Exploring the hidden human urinary proteome via ligand library beads [J].
Castagna, A ;
Cecconi, D ;
Sennels, L ;
Rappsilber, J ;
Guerrier, L ;
Fortis, F ;
Boschetti, E ;
Lomas, L ;
Rigetti, PG .
JOURNAL OF PROTEOME RESEARCH, 2005, 4 (06) :1917-1930
[6]  
Celis JE, 2000, ELECTROPHORESIS, V21, P2115
[7]  
CLARK PMS, 1980, CLIN CHEM, V26, P201
[8]  
Davis MT, 2001, PROTEOMICS, V1, P108, DOI 10.1002/1615-9861(200101)1:1<108::AID-PROT108>3.0.CO
[9]  
2-5
[10]   Depletion of multiple high-abundance proteins improves protein profiling capacities of human serum and plasma [J].
Echan, LA ;
Tang, HY ;
Ali-Khan, N ;
Lee, K ;
Speicher, DW .
PROTEOMICS, 2005, 5 (13) :3292-3303