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Protein identification methods in proteomics

Electrophoresis · 2000 · Vol. 21(6) · pp. 1145–1154
Kris GevaertJoël Vandekerckhove

Abstract

A combination of high-resolution two-dimensional (2-D) polyacrylamide gel electrophoresis, highly sensitive biological mass spectrometry, and the rapidly growing protein and DNA databases has paved the way for high-throughput proteomics. This review concentrates on protein identification. We first discuss the use of protein electroblotting and Edman sequencing as tools for de novo sequencing and protein identification. In the second part, we highlight matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) as one of the main contemporary analytical methods for linking gel-separated proteins to entries in sequence databases. In this context we describe the two main MALDI-MS-based identification methods: (i) peptide mass fingerprinting, and (ii) post-source decay (PSD) analysis. In the last part, we briefly emphasize the importance of sample preparation for obtaining highly sensitive and high-quality MALDI-MS spectra.

Mass Spectrometry Techniques and ApplicationsAdvanced Proteomics Techniques and ApplicationsMetabolomics and Mass Spectrometry StudiesElectroblottingMass spectrometryProteomicsPeptide mass fingerprintingBottom-up proteomicsMatrix-assisted laser desorption/ionizationContext (archaeology)ChromatographyTop-down proteomicsEdman degradation

MeSH terms

AnimalsHumansElectrophoresis, Gel, Two-DimensionalSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationProteome
Citations
324
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20.02
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