Post-Electrophoretic Identification of Oxidized Proteins
<p>The oxidative modification of proteins has been shown to play a major role in a number of human diseases. However, the ability to identify specific proteins that are most susceptible to oxidative modifications is difficult. Separation of proteins using polyacrylamide gel electrophoresis (PA...
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doaj-58e8eb7a4f8348c398e039e6277ebcd42020-11-24T21:53:21ZengBMCBiological Procedures Online1480-92222000-01-0121394510.1251/bpo17Post-Electrophoretic Identification of Oxidized Proteins Conrad CraigTalent JohnMalakowsky ChristinaGracy Robert<p>The oxidative modification of proteins has been shown to play a major role in a number of human diseases. However, the ability to identify specific proteins that are most susceptible to oxidative modifications is difficult. Separation of proteins using polyacrylamide gel electrophoresis (PAGE) offers the analytical potential for the recovery, amino acid sequencing, and identification of thousands of individual proteins from cells and tissues. We have developed a method to allow underivatized proteins to be electroblotted onto PVDF membranes before derivatization and staining. Since both the protein and oxidation proteins are quantifiable, the specific oxidation index of each protein can be determined. The optimal sequence and conditions for the staining process are (a) electrophoresis, (b) electroblotting onto PVDF membranes, (c) derivatization of carbonyls with 2,4-DNP, (d) immunostaining with anti DNP antibody, and (e) protein staining with colloidal gold.http://www.biologicalprocedures.com/bpo/arts/1/17/m17.htmproteinselectrophoresisoxidation-reduction |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Conrad Craig Talent John Malakowsky Christina Gracy Robert |
spellingShingle |
Conrad Craig Talent John Malakowsky Christina Gracy Robert Post-Electrophoretic Identification of Oxidized Proteins Biological Procedures Online proteins electrophoresis oxidation-reduction |
author_facet |
Conrad Craig Talent John Malakowsky Christina Gracy Robert |
author_sort |
Conrad Craig |
title |
Post-Electrophoretic Identification of Oxidized Proteins |
title_short |
Post-Electrophoretic Identification of Oxidized Proteins |
title_full |
Post-Electrophoretic Identification of Oxidized Proteins |
title_fullStr |
Post-Electrophoretic Identification of Oxidized Proteins |
title_full_unstemmed |
Post-Electrophoretic Identification of Oxidized Proteins |
title_sort |
post-electrophoretic identification of oxidized proteins |
publisher |
BMC |
series |
Biological Procedures Online |
issn |
1480-9222 |
publishDate |
2000-01-01 |
description |
<p>The oxidative modification of proteins has been shown to play a major role in a number of human diseases. However, the ability to identify specific proteins that are most susceptible to oxidative modifications is difficult. Separation of proteins using polyacrylamide gel electrophoresis (PAGE) offers the analytical potential for the recovery, amino acid sequencing, and identification of thousands of individual proteins from cells and tissues. We have developed a method to allow underivatized proteins to be electroblotted onto PVDF membranes before derivatization and staining. Since both the protein and oxidation proteins are quantifiable, the specific oxidation index of each protein can be determined. The optimal sequence and conditions for the staining process are (a) electrophoresis, (b) electroblotting onto PVDF membranes, (c) derivatization of carbonyls with 2,4-DNP, (d) immunostaining with anti DNP antibody, and (e) protein staining with colloidal gold. |
topic |
proteins electrophoresis oxidation-reduction |
url |
http://www.biologicalprocedures.com/bpo/arts/1/17/m17.htm |
work_keys_str_mv |
AT conradcraig postelectrophoreticidentificationofoxidizedproteins AT talentjohn postelectrophoreticidentificationofoxidizedproteins AT malakowskychristina postelectrophoreticidentificationofoxidizedproteins AT gracyrobert postelectrophoreticidentificationofoxidizedproteins |
_version_ |
1725872873481961472 |