| Literature DB >> 28138741 |
Pauline Bros1,2,3, Ralf D Josephs4, Norbert Stoppacher2, Guillaume Cazals5, Sylvain Lehmann3, Christophe Hirtz3, Robert I Wielgosz2, Vincent Delatour1.
Abstract
In metrology institutes, the state-of-the-art for purity analysis of peptides/proteins mainly addresses short and unfolded peptides. Important developments are anticipated for the characterization of nonlinear peptides or proteins. Hepcidin 1-25 is an interesting model system because this small protein contains four disulfide bridges with a particular connectivity that is difficult to reproduce and could induce a bias in quantification. Hepcidin 1-25 is involved in iron-related disorders and anemia, in an inflammatory context, and its clinical relevance in neurodegenerative disorders is under investigation. It is also an emerging biomarker. Recent inter-laboratory studies showed a need for standardization of hepcidin assay and the need to produce certified reference materials. This paper discusses two hepcidin standards from different synthesis pathways that have been characterized by high-resolution mass spectrometry and ion mobility mass spectrometry.Entities:
Keywords: Disulfide bridges; Hepcidin; High-resolution mass spectrometry; Ion mobility, conformers; Purity assessment
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Year: 2017 PMID: 28138741 DOI: 10.1007/s00216-017-0202-4
Source DB: PubMed Journal: Anal Bioanal Chem ISSN: 1618-2642 Impact factor: 4.142