4.5 Review

Functional genomics by mass spectrometry

Journal

FEBS LETTERS
Volume 480, Issue 1, Pages 25-31

Publisher

WILEY
DOI: 10.1016/S0014-5793(00)01773-7

Keywords

proteomics; protein-protein interaction; protein identification; genomics; nucleolus; signaling; phosphorylation

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Systematic analysis of the function of genes can take place at the oligonucleotide or protein level. The latter has the advantage of being closest to function, since it is proteins that perform most of the reactions necessary for the cell. For most protein based ('proteomic') approaches to gene function, mass spectrometry is the method of choice. Mass spectrometry can now identify proteins with very high sensitivity and medium to high throughput. New instrumentation for the analysis of the proteome has been developed including a MALDI hybrid quadrupole time of flight instrument which combines advantages of the mass finger printing and peptide sequencing methods for protein identification. New approaches include the isotopic labeling of proteins to obtain accurate quantitative data by mass spectrometry, methods to analyze peptides derived from crude protein mixtures and approaches to analyze large numbers of intact proteins by mass spectrometry directly. Examples from this laboratory illustrate biological problem solving by modern mass spectrometric techniques. These include the analysis of the structure and function of the nucleolus and the analysis of signaling complexes, (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.

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