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Article
Characterization and Quantitation of Membrane Proteomes Using Multidimensional MS-Based Proteomic Technologies
Expert Review of Proteomics
  • Josip Blonder
  • Thomas P. Conrads
  • Timothy D. Veenstra, Cedarville University
Document Type
Article
Publication Date
8-1-2004
DOI
10.1586/14789450.1.2.153
PubMed ID
15966810
Abstract

A major goal of proteomics is to develop methods that enable the systematic characterization of every protein within the cell or particular subcellular proteome using a single analytical platform. Although the equivalent has already been achieved in genomics, reaching this goal in proteomics represents a much greater challenge due to the wide dynamic range of protein expression, numerous post-translational modifications and remarkable physicochemical heterogeneity of proteins. A major analytical challenge has involved developing more effective means for proteome-scale investigations of membrane proteins, whose solubility differs drastically from that of cytoplasmic proteins. Fortunately, rapid progress has increased the ability to characterize this critically important class of proteins on a scale analogous to that of aqueous soluble proteins.

Keywords
  • Cell adhesion,
  • membrane proteins,
  • molecular,
  • protein conformation,
  • proteins,
  • proteomics,
  • solubility,
  • spectrometry,
  • mass
Citation Information
Josip Blonder, Thomas P. Conrads and Timothy D. Veenstra. "Characterization and Quantitation of Membrane Proteomes Using Multidimensional MS-Based Proteomic Technologies" Expert Review of Proteomics Vol. 1 Iss. 2 (2004) p. 153 - 163 ISSN: 1744-8387
Available at: http://works.bepress.com/timothy-veenstra/269/