Exploring the hidden human urinary proteome via ligand library beads

被引:189
作者
Castagna, A
Cecconi, D
Sennels, L
Rappsilber, J
Guerrier, L
Fortis, F
Boschetti, E
Lomas, L
Rigetti, PG
机构
[1] Univ Verona, Dept Clin & Expt Med, Unit Internal Med, I-37100 Verona, Italy
[2] Univ Verona, Dept Agr & Ind Biotechnol, I-37100 Verona, Italy
[3] IFOM, FIRC, Inst Mol Oncol Fdn, Milan, Italy
[4] Ciphergen Biosyst Inc, Fremont, CA 94555 USA
关键词
proteomics; dynamic range; ligand libraries; urinary proteins; hidden proteome; biochips;
D O I
10.1021/pr050153r
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The human urinary proteome has been reassessed and re-evaluated via a novel concentration/equalization technique, exploiting beads coated with hexameric peptide ligand libraries. These beads act by capturing the whole protein spectra contained in the sample, by drastically reducing the level of the most abundant species, while strongly concentrating the more dilute and rare ones. In a control urine sample, 134 unique proteins could be identified. The first bead eluate (in thiourea, urea, and CHAPS) permitted the identification of 317 gene products, whereas the second eluale (in 9 M urea, pH 3.8) allowed the identification of another 95 unique proteins. By eliminating redundancies, a total of 383 unique gene products could be identified in human urines. This represents a major increment as compared to data reported in recent literature. By comparing our data with those reported to the present, an additional 251 proteins could be added to the list, thus bringing the total unique gene products so far identified in human urines to ca.800 species.
引用
收藏
页码:1917 / 1930
页数:14
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