Purification and characterization of a 4-hydroxynonenal metabolizing glutathione S-transferase isozyme from bovine pulmonary microvessel endothelial cells
Previous studies have suggested that a group of structurally and immunologically related mammalian glutathione S-transferases (GSTs) which utilize 4-hydroxynonenal (4-HNE) as the preferred substrate and show glutathione peroxidase activity towards phospholipid hydroperoxides may be important for the...
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Published in | Biochimica et biophysica acta Vol. 1291; no. 3; pp. 182 - 188 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Netherlands
Elsevier B.V
06.12.1996
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Abstract | Previous studies have suggested that a group of structurally and immunologically related mammalian glutathione
S-transferases (GSTs) which utilize 4-hydroxynonenal (4-HNE) as the preferred substrate and show glutathione peroxidase activity towards phospholipid hydroperoxides may be important for the defense of cells against lipid peroxidation. In present studies we have purified and characterized GST isozymes of bovine pulmonary microvessel endothelial (BPMVE) cells. The results of these studies indicate that BPMVE cells express relatively high amounts of a GST isozyme which utilizes 4-HNE as the preferred substrate. This GST isozyme purified to homogeneity from BPMVE cells showed remarkably high specific activity towards 4-HNE (48.3 units/mg protein) and had similar immunological, kinetic, and structural characteristics as reported for mouse enzyme mGSTA4-4 and other mammalian GSTs of this group. Since the endothelial cells are exposed to constant oxidative stress, we suggest that this GST isozyme may be important for the defense of these cells against lipid peroxidation. |
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AbstractList | Previous studies have suggested that a group of structurally and immunologically related mammalian glutathione S-transferases (GSTs) which utilize 4-hydroxynonenal (4-HNE) as the preferred substrate and show glutathione peroxidase activity towards phospholipid hydroperoxides may be important for the defense of cells against lipid peroxidation. In present studies we have purified and characterized GST isozymes of bovine pulmonary microvessel endothelial (BPMVE) cells. The results of these studies indicate that BPMVE cells express relatively high amounts of a GST isozyme which utilizes 4-HNE as the preferred substrate. This GST isozyme purified to homogeneity from BPMVE cells showed remarkably high specific activity towards 4-HNE (48.3 units/mg protein) and had similar immunological, kinetic, and structural characteristics as reported for mouse enzyme mGSTA4-4 and other mammalian GSTs of this group. Since the endothelial cells are exposed to constant oxidative stress, we suggest that this GST isozyme may be important for the defense of these cells against lipid peroxidation. Previous studies have suggested that a group of structurally and immunologically related mammalian glutathione S-transferases (GSTs) which utilize 4-hydroxynonenal (4-HNE) as the preferred substrate and show glutathione peroxidase activity towards phospholipid hydroperoxides may be important for the defense of cells against lipid peroxidation. In present studies we have purified and characterized GST isozymes of bovine pulmonary microvessel endothelial (BPMVE) cells. The results of these studies indicate that BPMVE cells express relatively high amounts of a GST isozyme which utilizes 4-HNE as the preferred substrate. This GST isozyme purified to homogeneity from BPMVE cells showed remarkably high specific activity towards 4-HNE (48.3 units/mg protein) and had similar immunological, kinetic, and structural characteristics as reported for mouse enzyme mGSTA4-4 and other mammalian GSTs of this group. Since the endothelial cells are exposed to constant oxidative stress, we suggest that this GST isozyme may be important for the defense of these cells against lipid peroxidation.Previous studies have suggested that a group of structurally and immunologically related mammalian glutathione S-transferases (GSTs) which utilize 4-hydroxynonenal (4-HNE) as the preferred substrate and show glutathione peroxidase activity towards phospholipid hydroperoxides may be important for the defense of cells against lipid peroxidation. In present studies we have purified and characterized GST isozymes of bovine pulmonary microvessel endothelial (BPMVE) cells. The results of these studies indicate that BPMVE cells express relatively high amounts of a GST isozyme which utilizes 4-HNE as the preferred substrate. This GST isozyme purified to homogeneity from BPMVE cells showed remarkably high specific activity towards 4-HNE (48.3 units/mg protein) and had similar immunological, kinetic, and structural characteristics as reported for mouse enzyme mGSTA4-4 and other mammalian GSTs of this group. Since the endothelial cells are exposed to constant oxidative stress, we suggest that this GST isozyme may be important for the defense of these cells against lipid peroxidation. Previous studies have suggested that a group of structurally and immunologically related mammalian glutathione S-transferases (GSTs) which utilize 4-hydroxynonenal (4-HNE) as the preferred substrate and show glutathione peroxidase activity towards phospholipid hydroperoxides may be important for the defense of cells against lipid peroxidation. In present studies we have purified and characterized GST isozymes of bovine pulmonary microvessel endothelial (BPMVE) cells. The results of these studies indicate that BPMVE cells express relatively high amounts of a GST isozyme which utilizes 4-HNE as the preferred substrate. This GST isozyme purified to homogeneity from BPMVE cells showed remarkably high specific activity towards 4-HNE (48.3 units/mg protein) and had similar immunological, kinetic, and structural characteristics as reported for mouse enzyme mGSTA4-4 and other mammalian GSTs of this group. Since the endothelial cells are exposed to constant oxidative stress, we suggest that this GST isozyme may be important for the defense of these cells against lipid peroxidation. |
Author | He, Nong-Gao Awasthi, Yogesh C Awasthi, Sanjay Singhal, Sharad S Zimniak, Piotr Partridge, Catherine A Chaubey, Meena |
Author_xml | – sequence: 1 givenname: Nong-Gao surname: He fullname: He, Nong-Gao organization: Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, 7.138 Medical Research Bldg., Galveston, TX 77555-1067, USA – sequence: 2 givenname: Sharad S surname: Singhal fullname: Singhal, Sharad S organization: Department of Internal Medicine, University of Texas Medical Branch, Galveston, TX 77555-1067, USA – sequence: 3 givenname: Meena surname: Chaubey fullname: Chaubey, Meena organization: Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, 7.138 Medical Research Bldg., Galveston, TX 77555-1067, USA – sequence: 4 givenname: Sanjay surname: Awasthi fullname: Awasthi, Sanjay organization: Department of Internal Medicine, University of Texas Medical Branch, Galveston, TX 77555-1067, USA – sequence: 5 givenname: Piotr surname: Zimniak fullname: Zimniak, Piotr organization: Department of Internal Medicine and Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, and McClellan VA Hospital, Little Rock, AK 72205, USA – sequence: 6 givenname: Catherine A surname: Partridge fullname: Partridge, Catherine A organization: Department of Biochemistry and Molecular Biology, Albany Medical College, Albany, NY 12208, USA – sequence: 7 givenname: Yogesh C surname: Awasthi fullname: Awasthi, Yogesh C organization: Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, 7.138 Medical Research Bldg., Galveston, TX 77555-1067, USA |
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Keywords | PBS SDS 4-Hydroxynonenal Bovine Hepes Lipid peroxidation BPMVE GST CDNB DMEM 4-HNE P/S FBS ROS Glutathione S-transferase GSH Microvessel endothelial cell |
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S-transferases (GSTs) which utilize... Previous studies have suggested that a group of structurally and immunologically related mammalian glutathione S-transferases (GSTs) which utilize... |
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SubjectTerms | 4-Hydroxynonenal Aldehydes - metabolism Amino Acid Sequence Animals Bovine Cattle Cells, Cultured Electrophoresis, Polyacrylamide Gel Endothelium, Vascular - cytology Endothelium, Vascular - enzymology Glutathione S-transferase Glutathione Transferase - isolation & purification Glutathione Transferase - metabolism Isoenzymes - isolation & purification Isoenzymes - metabolism Lipid Peroxidation Lung - blood supply Microvessel endothelial cell Molecular Sequence Data Peptide Mapping Sequence Homology, Amino Acid |
Title | Purification and characterization of a 4-hydroxynonenal metabolizing glutathione S-transferase isozyme from bovine pulmonary microvessel endothelial cells |
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