A novel targeted proteomics method for identification and relative quantitation of difference in nitration degree of OGDH between healthy and diabetic mouse. Issue 21 (November 2014)
- Record Type:
- Journal Article
- Title:
- A novel targeted proteomics method for identification and relative quantitation of difference in nitration degree of OGDH between healthy and diabetic mouse. Issue 21 (November 2014)
- Main Title:
- A novel targeted proteomics method for identification and relative quantitation of difference in nitration degree of OGDH between healthy and diabetic mouse
- Authors:
- Yu, Qing
Liu, Bin
Ruan, Dandan
Niu, Chao
Shen, Jiayi
Ni, Maowei
Cong, Weitao
Lu, Xianghong
Jin, Litai - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>For analysis of nitration modification of α oxoglutarate dehydrogenase (α‐OGDH) induced by diabetes, a targeted proteomics strategy was developed through the use of Skyline. All peptides containing Y and W of the target proteins were nitrated in silico and output to produce parallel reaction monitoring (PRM) or SRM method for nitration analysis. A nitrated casein mixture was used as standard protein to assess the feasibility of this method. The results demonstrated the availability of this strategy for nitration identification, and subsequently this method was used to analyze the nitration of α‐OGDH from myocardial tissue extracts of diabetic mouse. The PRM method was primarily generated by Skyline for identification of the actual nitrated peptides from all possible nitrated peptides of α‐OGDH due to the complexity of α‐OGDH. The PRM‐based data were analyzed by SEQUEST, and transitions of the identified nitrated peptides were used to develop an SRM method for relative quantitation of nitration degree. The nitration degree of α‐OGDH for diabetic mouse is higher than that for control mouse, indicating that α‐OGDH of the diabetic mouse suffered from more intense oxidative damage. We believe that this approach for obtaining information regarding nitration will facilitate the study of other PTMs in complex mixtures.</p> </abstract>
- Is Part Of:
- Proteomics. Volume 14:Issue 21/22(2014)
- Journal:
- Proteomics
- Issue:
- Volume 14:Issue 21/22(2014)
- Issue Display:
- Volume 14, Issue 21/22 (2014)
- Year:
- 2014
- Volume:
- 14
- Issue:
- 21/22
- Issue Sort Value:
- 2014-0014-NaN-0000
- Page Start:
- 2417
- Page End:
- 2426
- Publication Date:
- 2014-11
- Subjects:
- Proteins -- Separation -- Periodicals
Bioinformatics -- Periodicals
Proteomics -- Periodicals
Genomes -- Periodicals
Molecular genetics -- Periodicals
572.605 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1615-9861 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pmic.201400274 ↗
- Languages:
- English
- ISSNs:
- 1615-9853
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.178000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3774.xml