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Integration with the human genome of peptide sequences obtained by high-throughput mass spectrometry

Frank Desiere* 1,2 email, Eric W Deutsch* 2 email, Alexey I Nesvizhskii* 2 email, Parag Mallick* 2 email, Nichole L King2 email, Jimmy K Eng2 email, Alan Aderem2 email, Rose Boyle2, Erich Brunner2,3, Samuel Donohoe2 email, Nelson Fausto4, Ernst Hafen3, Lee Hood2 email, Michael G Katze5, Kathleen A Kennedy2 email, Floyd Kregenow2 email, Hookeun Lee2 email, Biaoyang Lin2 email, Dan Martin2 email, Jeffrey A Ranish2 email, David J Rawlings6, Lawrence E Samelson7, Yuzuru Shiio2 email, Julian D Watts2 email, Bernd Wollscheid2 email, Michael E Wright2 email, Wei Yan2 email, Lihong Yang8, Eugene C Yi2 email, Hui Zhang2 email and Ruedi Aebersold2,9 email

1Nestlé Research Center, 1000 Lausanne 26, Switzerland

2Institute for Systems Biology, 1441 N 34th Street, Seattle, WA 98103, USA

3Institute of Zoology, University of Zürich, CH-8057 Zürich, Switzerland

4Department of Pathology, University of Washington, Seattle, WA 98195-7705, USA

5Department of Microbiology, School of Medicine, University of Washington, Seattle, WA 98195, USA

6Department of Pediatrics, University of Washington, Seattle, WA 98195, USA

7National Cancer Institute, 37 Convent Drive, Bethesda, MD 20892, USA

8North Shore Long Island Jewish Research Institute, 350 Community Drive, Manhasset, NY 11030, USA

9Institute of Biotechnology, Swiss Federal Institute of Technology, ETH Hönggerberg, HPT E 78, CH-8093 Zürich, Switzerland

author email corresponding author email* Contributed equally

Genome Biology 2004, 6:R9doi:10.1186/gb-2004-6-1-r9

Published: 10 December 2004

Subject areas: Genome studies, Biochemistry and structural biology, Methods

Abstract

A crucial aim upon the completion of the human genome is the verification and functional annotation of all predicted genes and their protein products. Here we describe the mapping of peptides derived from accurate interpretations of protein tandem mass spectrometry (MS) data to eukaryotic genomes and the generation of an expandable resource for integration of data from many diverse proteomics experiments. Furthermore, we demonstrate that peptide identifications obtained from high-throughput proteomics can be integrated on a large scale with the human genome. This resource could serve as an expandable repository for MS-derived proteome information.


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