Proteomics application exercise of the Swiss Proteomics Society:: Report of the SPS'02 session

被引:6
作者
Binz, PA
Abdi, F
Affolter, M
Allard, L
Barblan, J
Bhardwaj, S
Bienvenut, WV
Bulet, P
Burgess, J
Carrette, O
Corthals, G
Delalande, F
Diemer, H
Favreau, P
Giuliano, E
Gueguen, Y
Guillaume, E
Hahner, S
Man, P
Michalet, S
Neri, D
Noukakis, D
Palagi, P
Paroutaud, P
Pimenta, DC
Quadroni, M
Resemann, A
Richert, S
Rybak, J
Sanchez, JC
Scherl, A
Scheurer, S
Hufnagel, US
Siethoff, C
Suckau, D
van Dorsselaer, A
Redeker, WW
Walter, N
Stöcklin, R
机构
[1] Ctr Med Univ Geneva, Swiss Inst Bioinformat, Proteome Informat Grp, CH-1211 Geneva 4, Switzerland
[2] Appl Biosyst Inc, Framingham, MA USA
[3] Nestec Ltd, Lausanne, Switzerland
[4] Univ Hosp Geneva, LCCC, Biomed Proteom Res Grp, Geneva, Switzerland
[5] Univ Lausanne, Prot Anal Facil, CH-1066 Epalinges, Switzerland
[6] Atheris Labs, Geneva, Switzerland
[7] ULP, CNRS, Lab Spectrometrie Masse Bioorgan, Strasbourg, France
[8] Inst Pharmaceut Sci, Zurich, Switzerland
[9] Univ Montpellier, CNRS, UMR 5098, IFREMER, F-34059 Montpellier, France
[10] Bruker Dalton Bremen, Bremen, Germany
[11] Spectronex ThermoFinnigan, Basel, Switzerland
[12] FontisMedia, Lausanne, Switzerland
[13] Applera France, Courtaboeuf, France
[14] Ctr Appl Toxinol, Inst Butantan, Sao Paulo, Brazil
关键词
mass spectrometry; proteomics exercise; proteomics methods; tandem mass spectrometry;
D O I
10.1002/pmic.200300458
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
After the success of the mass spectrometry (MS) round table that was held at the first Swiss Proteomics Society congress (SPS'01) in Geneva, the SIPS has organized a proteomics application exercise and allocated a full session at the SPS'02 congress. The main objective was to encourage the exchange of expertise in protein identification, with a focus on the use of mass spectrometry, and to create a bridge between the users' questions and the instrument providers' solutions. Two samples were sent to fifteen interested labs, including academic groups and MS hardware providers. Participants were asked to identify and partially characterize the samples. They consisted of a complex mixture of peptide/proteins (sample A) and an almost pure recombinant peptide carrying post-translational modifications (sample B). Sample A was an extract of snake venom from the species Bothrops jararaca. Sample B was a recombinant and modified peptide derived from the shrimp Penaeus vannamei penaeidin 3a. The eight labs that returned results reported the use of a wide range of MS instrumentation and techniques. They mentioned a variety of time and manpower allocations. The origin of sample A was generally identified together with a number of database protein entries. The difficulty of the sample identification lay in the incomplete knowledge of the Bothrops species genome sequence and is discussed. Sample B was generally and correctly identified as penaeidin. However, only one group reported the full primary structure. Interestingly, the approaches were again varied and are discussed in the text.
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页码:1562 / 1566
页数:5
相关论文
共 2 条
[1]  
Stöcklin R, 2002, PROTEOMICS, V2, P825, DOI 10.1002/1615-9861(200207)2:7<825::AID-PROT825>3.0.CO
[2]  
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