Standard Guidelines for the Chromosome-Centric Human Proteome Project

被引:114
作者
Paik, Young-Ki [1 ,2 ]
Omenn, Gilbert S. [3 ]
Uhlen, Mathias [4 ]
Hanash, Samir [5 ]
Marko-Varga, Gyorgy [6 ]
Aebersold, Ruedi [7 ,8 ]
Bairoch, Amos [9 ,10 ]
Yamamoto, Tadashi [11 ]
Legrain, Pierre [12 ]
Lee, Hyoung-Joo [1 ,2 ]
Na, Keun [1 ,2 ]
Jeong, Seul-Ki [1 ,2 ]
He, Fuchu [13 ]
Binz, Pierre-Alain [9 ,10 ]
Nishimura, Toshihide [14 ]
Keown, Paul [15 ]
Baker, Mark S. [16 ]
Yoo, Jong Shin [17 ]
Garin, Jerome [18 ]
Archakov, Alexander [19 ]
Bergeron, John [20 ]
Salekdeh, Ghasem Hosseini [21 ]
Hancock, William S. [1 ,2 ,22 ]
机构
[1] Yonsei Univ, Yonsei Proteome Res Ctr, Seoul 120749, South Korea
[2] Yonsei Univ, Dept Integrated Omics Biomed Sci, World Class Univ Program, Seoul 120749, South Korea
[3] Univ Michigan, Ctr Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
[4] Royal Inst Technol, Stockholm, Sweden
[5] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
[6] Lund Univ, Lund, Sweden
[7] ETH, Dept Biol, Inst Mol Syst Biol, Zurich, Switzerland
[8] Univ Zurich, Fac Sci, CH-8006 Zurich, Switzerland
[9] SIB, Geneva, Switzerland
[10] Univ Geneva, Geneva, Switzerland
[11] Niigata Univ, Grad Sch Med & Dent Sci, Niigata, Japan
[12] Ecole Polytech, Palaiseau, France
[13] Beijing Proteome Res Ctr, Beijing, Peoples R China
[14] Tokyo Med & Dent Univ, Dept Surg 1, Tokyo, Japan
[15] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[16] Macquarie Univ, N Ryde, NSW 2109, Australia
[17] Korea Basic Sci Inst, Ochang, South Korea
[18] CEA, Grenoble, France
[19] Russian Acad Med Sci, Moscow, Russia
[20] McGill Univ, Montreal, PQ, Canada
[21] Royan Inst, Tehran, Iran
[22] Northeastern Univ, Boston, MA 02115 USA
基金
新加坡国家研究基金会;
关键词
antibody; Biology/Disease-Driven Human Proteome Project; Chromosome-Centric Human Proteome Project; Human Genome Project; Human Proteome Project; Human Proteome Organization; knowledge-base; mass spectrometry; MASS-SPECTROMETRY; IDENTIFICATION; PROTEINS; GENOME; RATES;
D O I
10.1021/pr200824a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The objective of the international Chromosome-Centric Human Proteome Project (C-HPP) is to map and annotate all proteins encoded by the genes on each human chromosome. The C-FIPP consortium was established to organize a collaborative network among the research teams responsible for protein mapping of individual chromosomes and to identify compelling biological and genetic mechanisms influencing colocated genes and their protein products. The C-HPP aims to foster the development of proteome analysis and integration of the findings from related molecular -omics technology platforms through collaborations among universities, industries, and private research groups. The C-HPP consortium leadership has elicited broad input for standard guidelines to manage these international efforts more efficiently by mobilizing existing resources and collaborative networks. The C-HPP guidelines set out the collaborative consensus of the C-HPP teams, introduce topics associated with experimental approaches, data production, quality control, treatment, and transparency of data, governance of the consortium, and collaborative benefits. A companion approach for the Biology and Disease-Driven HPP (B/D-HPP) component of the Human Proteome Project is currently being organized, building upon the Human Proteome Organization's organ-based and biofluid-based initiatives (www.hupo.org/research). The common application of these guidelines in the participating laboratories is expected to facilitate the goal of a comprehensive analysis of the human proteome.
引用
收藏
页码:2005 / 2013
页数:9
相关论文
共 28 条
[21]   Peptide Labeling with Isobaric Tags Yields Higher Identification Rates Using iTRAQ 4-Plex Compared to TMT 6-Plex and iTRAQ 8-Plex on LTQ Orbitrap [J].
Pichler, Peter ;
Koecher, Thomas ;
Holzmann, Johann ;
Mazanek, Michael ;
Taus, Thomas ;
Ammerer, Gustav ;
Mechtler, Karl .
ANALYTICAL CHEMISTRY, 2010, 82 (15) :6549-6558
[22]  
Picotti P, 2010, NAT METHODS, V7, P43, DOI [10.1038/NMETH.1408, 10.1038/nmeth.1408]
[23]   Absolute quantification of microbial proteomes at different states by directed mass spectrometry [J].
Schmidt, Alexander ;
Beck, Martin ;
Malmstroem, Johan ;
Lam, Henry ;
Claassen, Manfred ;
Campbell, David ;
Aebersold, Ruedi .
MOLECULAR SYSTEMS BIOLOGY, 2011, 7
[24]   Value of Using Multiple Proteases for Large-Scale Mass Spectrometry-Based Proteomics [J].
Swaney, Danielle L. ;
Wenger, Craig D. ;
Coon, Joshua J. .
JOURNAL OF PROTEOME RESEARCH, 2010, 9 (03) :1323-1329
[25]   Antibody-based proteomics for human tissue profiling [J].
Uhlen, M ;
Ponten, F .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (04) :384-393
[26]  
Uhlen M., 2011, MOL CELL PROTEOMICS, V10
[27]   Towards standard protocols and guidelines for urine proteomics: A report on the Human Kidney and Urine Proteome Project (HKUPP) symposium and workshop - 6 October 2007, Seoul, Korea and 1 November 2007, San Francisco, CA, USA [J].
Yamamoto, Tadashi ;
Langham, Robyn G. ;
Ronco, Pierre ;
Knepper, Mark A. ;
Thongboonkerd, Visith .
PROTEOMICS, 2008, 8 (11) :2156-2159
[28]   Proteomic parsimony through bipartite graph analysis improves accuracy and transparency [J].
Zhang, Bing ;
Chambers, Matthew C. ;
Tabb, David L. .
JOURNAL OF PROTEOME RESEARCH, 2007, 6 (09) :3549-3557