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Heterogeneity in human cardiac troponin I standards.

Authors :
Bunk DM
Dalluge JJ
Welch MJ
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.

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