Literature DB >> 18629005

Quantitative proteomics of lymphocytes.

Ivan Lefkovits1.   

Abstract

Lymphocytes are the best-studied higher eukaryote cells. In this report, quantitative relationships of the protein components in resting cell, blast cell and plasma cell types are evaluated. The comparison of these cell types leads to the conclusion that resting cells synthesize about one-twentieth of the protein species as compared to blast cells. Blast cells seem to be metabolically the most robust lymphocyte type. Plasma cells are geared towards synthesis of one main product (antibody in B plasma cells), while most of the synthesis of other protein species (including those for housekeeping and repair) decreases as the messages decay. Although the data presented in this communication allow a meaningful comparison of three cell populations, they are far from providing a full picture. Both silver staining and radiofluorography depict only proteins of high or intermediate abundance. Silver staining misses most proteins present at <10 000 copies/cell, while radiofluorography misses all those proteins with slow turnover (and those with no methionine residue in their sequence). The detection of 1100 spots in the blast cell-related radiofluorograph includes visualization of some 97-99% of protein mass, but some 3900 polypeptide species in the remaining 1-3% of protein mass will pass undetected. This protein mass (0.7-2 pg) reflects some 2500-7500 copies of each of those 3900 polypeptide species that are present in the cell below the detection limit. The work emphasizes that full understanding of cellular function can be achieved only if quantitative aspects of cell inventory are considered.

Entities:  

Year:  2003        PMID: 18629005      PMCID: PMC2447287          DOI: 10.1002/cfg.322

Source DB:  PubMed          Journal:  Comp Funct Genomics        ISSN: 1531-6912


  16 in total

Review 1.  Global analysis of gene expression in cells of the immune system I. Analytical limitations in obtaining sequence information on polypeptides in two-dimensional gel spots.

Authors:  I Lefkovits; J R Kettman; J R Frey
Journal:  Electrophoresis       Date:  2000-07       Impact factor: 3.535

2.  Clonal proteomics: one gene - family of proteins.

Authors:  John R Kettman; Christopher Coleclough; Johann Rudolf Frey; Ivan Lefkovits
Journal:  Proteomics       Date:  2002-06       Impact factor: 3.984

3.  High resolution two-dimensional electrophoresis of proteins.

Authors:  P H O'Farrell
Journal:  J Biol Chem       Date:  1975-05-25       Impact factor: 5.157

4.  Two new staining procedures for quantitative estimation of proteins on electrophoretic strips.

Authors:  S Fazekas de St Groth; R G Webster; A Datyner
Journal:  Biochim Biophys Acta       Date:  1963-05-14

5.  Parameters of the labeling of mitogen-activated murine lymphocytes by [35S]methionine for two-dimensional gel electrophoresis. I. Effect of culture conditions.

Authors:  J R Kettman; L Kuhn; P Young; I Lefkovits
Journal:  J Immunol Methods       Date:  1986-04-03       Impact factor: 2.303

6.  Prospective partition analysis of independently assorted sets. Accessory elements supporting clonal lymphoid activation by mitogens.

Authors:  J Kettman; K Burnham; I Lefkovits
Journal:  J Immunol Methods       Date:  1988-11-10       Impact factor: 2.303

7.  Protein mapping by combined isoelectric focusing and electrophoresis of mouse tissues. A novel approach to testing for induced point mutations in mammals.

Authors:  J Klose
Journal:  Humangenetik       Date:  1975

8.  Changes in the protein pattern of murine B cells after mitogenic stimulation.

Authors:  J Kettman; I Lefkovits
Journal:  Eur J Immunol       Date:  1984-09       Impact factor: 5.532

9.  An approach to molecular analysis of T-cell clones by two-dimensional gel electrophoresis: is there interclonal and intraclonal heterogeneity?

Authors:  J Kettman; I Lefkovits
Journal:  Clin Chem       Date:  1984-12       Impact factor: 8.327

10.  Analytical techniques for cell fractions. XXI. Two-dimensional analysis of serum and tissue proteins: multiple isoelectric focusing.

Authors:  N G Anderson; N L Anderson
Journal:  Anal Biochem       Date:  1978-04       Impact factor: 3.365

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