| Literature DB >> 25753013 |
Didia Coelho Graça1, Ralf Hartmer, Wolfgang Jabs, Photis Beris, Lorella Clerici, Carsten Stoermer, Kaveh Samii, Denis Hochstrasser, Yury O Tsybin, Alexander Scherl, Pierre Lescuyer.
Abstract
Hemoglobin disorder diagnosis is a complex procedure combining several analytical steps. Due to the lack of specificity of the currently used protein analysis methods, the identification of uncommon hemoglobin variants (proteoforms) can become a hard task to accomplish. The aim of this work was to develop a mass spectrometry-based approach to quickly identify mutated protein sequences within globin chain variants. To reach this goal, a top-down electron transfer dissociation mass spectrometry method was developed for hemoglobin β chain analysis. A diagnostic product ion list was established with a color code strategy allowing to quickly and specifically localize a mutation in the hemoglobin β chain sequence. The method was applied to the analysis of rare hemoglobin β chain variants and an (A)γ-β fusion protein. The results showed that the developed data analysis process allows fast and reliable interpretation of top-down electron transfer dissociation mass spectra by nonexpert users in the clinical area.Entities:
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Year: 2015 PMID: 25753013 DOI: 10.1007/s00216-015-8525-5
Source DB: PubMed Journal: Anal Bioanal Chem ISSN: 1618-2642 Impact factor: 4.142