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A Proteomic Analysis of Human Hemodialysis Fluid
The vascular compartment is an easily accessible compartment that provides an opportunity to measure analytes for diagnostic, prognostic, or therapeutic indications. Both serum and plasma have been analyzed extensively by proteomic approaches in an effort to catalog all proteins and polypeptides. Li...
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Published in: | Molecular & cellular proteomics 2005-05, Vol.4 (5), p.637-650 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The vascular compartment is an easily accessible compartment that provides an opportunity to measure analytes for diagnostic,
prognostic, or therapeutic indications. Both serum and plasma have been analyzed extensively by proteomic approaches in an
effort to catalog all proteins and polypeptides. Limitations of such approaches in obtaining a comprehensive catalog of proteins
include the fact that a handful of proteins constitute over 90% of plasma protein content and that the renal glomeruli filter
out proteins and polypeptides that are smaller than 66 kDa from blood. We chose to study hemodialysis fluid because it contains
a higher concentration of small proteins and polypeptides and is also simultaneously depleted of the most abundant proteins
present in blood. Using gel electrophoresis in combination with LC-MS/MS, we identified 292 proteins of which greater than
70% had not been previously identified from serum or plasma. More than half of the proteins identified from the hemodialysis
fluid were smaller than 40 kDa. We also found 50 N-terminally acetylated peptides that allowed us to unambiguously map the
N termini of mature forms of the corresponding proteins. Several identified proteins, including cytokines, were only present
as predicted transcripts in data bases and thus represent novel proteins. The proteins identified in this study could serve
as biomarkers in serum using more sensitive methods such as ELISA-specific antibodies. |
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ISSN: | 1535-9476 1535-9484 |
DOI: | 10.1074/mcp.M500042-MCP200 |