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Heterogeneity in human cardiac troponin I standards.
- Source :
-
Analytical biochemistry [Anal Biochem] 2000 Sep 10; Vol. 284 (2), pp. 191-200. - Publication Year :
- 2000
-
Abstract
- The LC-MS analysis of recombinant cardiac troponin I (cTnI) and cTnI extracted from human hearts showed a high degree of structural heterogeneity among all samples. The examined recombinant cTnI samples indicated posttranslational modifications, presumably due to their purification (i.e., 2-mercaptoethanol adducts and carbamylation) and related to their expression (i.e., an N-terminal expression tag). The extracted cTnI samples, while having a higher degree of structural heterogeneity, showed less structural variance between samples than the recombinant proteins. The LC-MS analysis of the extracted cTnI samples provided evidence of posttranslational modification by phosphorylation, acetylation, proteolytic cleavage, and intrachain disulfide bond formation.
- Subjects :
- Amino Acid Sequence
Chromatography, Liquid
Humans
Mass Spectrometry
Molecular Sequence Data
Recombinant Proteins analysis
Recombinant Proteins chemistry
Recombinant Proteins standards
Spectrophotometry, Ultraviolet
Troponin I analysis
Troponin I chemistry
Myocardium chemistry
Troponin I standards
Subjects
Details
- Language :
- English
- ISSN :
- 0003-2697
- Volume :
- 284
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Analytical biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 10964401
- Full Text :
- https://doi.org/10.1006/abio.2000.4710