Accurate and precise quantification of Cu, Zn-SOD in human red blood cells using species-specific double and triple IDMS. Issue 9 (7th April 2016)
- Record Type:
- Journal Article
- Title:
- Accurate and precise quantification of Cu, Zn-SOD in human red blood cells using species-specific double and triple IDMS. Issue 9 (7th April 2016)
- Main Title:
- Accurate and precise quantification of Cu, Zn-SOD in human red blood cells using species-specific double and triple IDMS
- Authors:
- Gleitzmann, Julia
Raab, Andrea
Schulze, Dirk
Wätzig, Hermann
Feldmann, Jörg
Swart, Claudia - Abstract:
- Abstract : Species-specific double and triple isotope dilution mass spectrometry (IDMS) was applied for the precise quantification of Cu, Zn-SOD in human erythrocytes. Abstract : Cu, Zn-superoxide dismutase (SOD1) is a protein involved in the antioxidant defense system of the body responsible for the dismutation of the superoxide anion. It contains two Cu and two Zn ions per molecule. As this protein is also involved in several diseases it is used in clinical diagnostics as a biomarker, which requires the accurate and reliable determination of SOD1. Therefore, a candidate reference measurement procedure for the quantification of this protein in human erythrocytes was developed using species-specific isotope dilution mass spectrometry (IDMS), a method giving results traceable to the International System of Units (SI). The measurement procedure was validated with regard to a metrological point of view. Commercially available SOD1 was thoroughly characterized to be used as a pure protein calibration standard in IDMS approaches. Furthermore, 65 Cu and 67 Zn labeled SOD1 was produced to be used as a spike material required for species-specific IDMS. Finally, SOD1 was quantified in human erythrocytes using both double and triple IDMS and a complete uncertainty budget for both approaches was estimated according to the Guide to the Expression of Uncertainty in Measurement (GUM). A calculated mass fraction of SOD1 with its associated expanded uncertainty of (63.94 ± 0.93) μg g −1 ( nAbstract : Species-specific double and triple isotope dilution mass spectrometry (IDMS) was applied for the precise quantification of Cu, Zn-SOD in human erythrocytes. Abstract : Cu, Zn-superoxide dismutase (SOD1) is a protein involved in the antioxidant defense system of the body responsible for the dismutation of the superoxide anion. It contains two Cu and two Zn ions per molecule. As this protein is also involved in several diseases it is used in clinical diagnostics as a biomarker, which requires the accurate and reliable determination of SOD1. Therefore, a candidate reference measurement procedure for the quantification of this protein in human erythrocytes was developed using species-specific isotope dilution mass spectrometry (IDMS), a method giving results traceable to the International System of Units (SI). The measurement procedure was validated with regard to a metrological point of view. Commercially available SOD1 was thoroughly characterized to be used as a pure protein calibration standard in IDMS approaches. Furthermore, 65 Cu and 67 Zn labeled SOD1 was produced to be used as a spike material required for species-specific IDMS. Finally, SOD1 was quantified in human erythrocytes using both double and triple IDMS and a complete uncertainty budget for both approaches was estimated according to the Guide to the Expression of Uncertainty in Measurement (GUM). A calculated mass fraction of SOD1 with its associated expanded uncertainty of (63.94 ± 0.93) μg g −1 ( n = 30) for double and (64.02 ± 0.96) μg g −1 ( n = 30) for triple IDMS was obtained. … (more)
- Is Part Of:
- Journal of analytical atomic spectrometry. Volume 31:Issue 9(2016:Sep.)
- Journal:
- Journal of analytical atomic spectrometry
- Issue:
- Volume 31:Issue 9(2016:Sep.)
- Issue Display:
- Volume 31, Issue 9 (2016)
- Year:
- 2016
- Volume:
- 31
- Issue:
- 9
- Issue Sort Value:
- 2016-0031-0009-0000
- Page Start:
- 1922
- Page End:
- 1928
- Publication Date:
- 2016-04-07
- Subjects:
- Atomic spectra -- Periodicals
Atomic absorption spectroscopy -- Periodicals
543.0858 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/ja#!recentarticles&adv ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5ja00459d ↗
- Languages:
- English
- ISSNs:
- 0267-9477
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4928.200000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 604.xml