Quantification of Type I Collagen α1 in Culture Medium Using Nano-Liquid Chromatography Tandem Mass Spectrometry

Type I collagen, which consists of two α1 and one α2 chains, is an abundant extracellular matrix (ECM) protein. Changes in type I collagen are often associated with various diseases including fibrosis, osteogenesis imperfecta (OI), and Ehlers-Danlos syndrome (EDS). In the present study, we developed...

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Veröffentlicht in:Shimane Journal of Medical Science 2021, Vol.38(1), pp.1-5
Hauptverfasser: GONG, Ao, YAMADA, Kazuo, JING, Li, TAKESHITA, Haruo, MATSUMOTO, Ken-ichi
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Sprache:eng ; jpn
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Zusammenfassung:Type I collagen, which consists of two α1 and one α2 chains, is an abundant extracellular matrix (ECM) protein. Changes in type I collagen are often associated with various diseases including fibrosis, osteogenesis imperfecta (OI), and Ehlers-Danlos syndrome (EDS). In the present study, we developed a method for quantification of type I collagen α1 (COL1A1) in a culture medium of LX-2 human hepatic stellate cells by using nano-liquid chromatography tandem mass spectrometry (nano-LC/MS/MS). After selecting a specific peptide of COL1A1, unlabeled and stable isotope-labeled peptides were used for quantitative analysis of COL1A1 by nano-LC/MS/MS. The concentration of secreted COL1A1 in the LX-2 cell culture medium was 38.78 ng/mL. The results indicate that this method is useful for quantifying COL1A1 in a cell culture medium.
ISSN:0386-5959
2433-2410
DOI:10.51010/sjms.38.1_1