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Quantitative Proteomics of Lymphocytes
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...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447287/ https://www.ncbi.nlm.nih.gov/pubmed/18629005 http://dx.doi.org/10.1002/cfg.322 |
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author | Lefkovits, Ivan |
author_facet | Lefkovits, Ivan |
author_sort | Lefkovits, Ivan |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2447287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-24472872008-07-14 Quantitative Proteomics of Lymphocytes Lefkovits, Ivan Comp Funct Genomics Research Article 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. Hindawi Publishing Corporation 2003-10 /pmc/articles/PMC2447287/ /pubmed/18629005 http://dx.doi.org/10.1002/cfg.322 Text en Copyright © 2003 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lefkovits, Ivan Quantitative Proteomics of Lymphocytes |
title | Quantitative Proteomics of Lymphocytes |
title_full | Quantitative Proteomics of Lymphocytes |
title_fullStr | Quantitative Proteomics of Lymphocytes |
title_full_unstemmed | Quantitative Proteomics of Lymphocytes |
title_short | Quantitative Proteomics of Lymphocytes |
title_sort | quantitative proteomics of lymphocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447287/ https://www.ncbi.nlm.nih.gov/pubmed/18629005 http://dx.doi.org/10.1002/cfg.322 |
work_keys_str_mv | AT lefkovitsivan quantitativeproteomicsoflymphocytes |