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Proteomics application exercise of the Swiss Proteomics Society: report of the SPS'02 session
Authors:Binz Pierre-Alain  Abdi Fadi  Affolter Michael  Allard Laure  Barblan Jachen  Bhardwaj Sanjeev  Bienvenut Willy V  Bulet Philippe  Burgess Jennifer  Carrette Odile  Corthals Garry  Delalande François  Diemer Hélène  Favreau Philippe  Giuliano Elia  Gueguen Yannick  Guillaume Elisabeth  Hahner Stephanie  Man Petr  Michalet Sophie  Neri Dario  Noukakis Dimitrios  Palagi Patricia  Paroutaud Pierre  Pimenta Daniel Carvalho  Quadroni Manfredo  Resemann Anja  Richert Sophie  Rybak Jascha  Sanchez Jean-Charles  Scherl Alexander  Scheurer Simone  Schweiger Hufnagel Ulrike  Siethoff Christoph  Suckau Detlev  van Dorsselaer Alain
Affiliation:Swiss Institute of Bioinformatics (SIB), Centre Médical Universitaire, 1 Michel-Servet, CH-1211 Geneva 4, Switzerland.
Abstract:
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 SPS 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.
Keywords:
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