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Clinical method evaluation of hemoglobin S and C identification by top-down selected reaction monitoring and electron transfer dissociation.

Authors :
Lassout O
Hartmer R
Jabs W
Clerici L
Tsybin YO
Samii K
Vuilleumier N
Hochstrasser D
Scherl A
Lescuyer P
Coelho Graça D
Source :
Clinical proteomics [Clin Proteomics] 2019 Dec 17; Vol. 16, pp. 41. Date of Electronic Publication: 2019 Dec 17 (Print Publication: 2019).
Publication Year :
2019

Abstract

Background: Biological diagnosis of hemoglobin disorders is a complex process relying on the combination of several analytical techniques to identify Hb variants in a particular sample. Currently, hematology laboratories usually use high-performance liquid chromatography (HPLC), capillary electrophoresis and gel-based methods to characterize Hb variants. Co-elution and co-migration may represent major issues for precise identification of Hb variants, even for the most common ones such as Hb S and C.<br />Methods: We adapted a top-down selected reaction monitoring (SRM) electron transfer dissociation (ETD) mass spectrometry (MS) method to fit with a clinical laboratory environment. An automated analytical process with semi-automated data analysis compatible with a clinical practice was developed. A comparative study between a reference HPLC method and the MS assay was performed on 152 patient samples.<br />Results: The developed workflow allowed to identify with high specificity and selectivity the most common Hb variants (Hb S and Hb C). Concordance of the MS-based approach with HPLC was 71/71 (100%) for Hb S and 11/11 (100%) for Hb C.<br />Conclusions: This top-down SRM ETD method can be used in a clinical environment to detect Hb S and Hb C.<br />Competing Interests: Competing interestsThe authors declare that they have no competing interests.<br /> (© The Author(s) 2019.)

Details

Language :
English
ISSN :
1542-6416
Volume :
16
Database :
MEDLINE
Journal :
Clinical proteomics
Publication Type :
Academic Journal
Accession number :
31889938
Full Text :
https://doi.org/10.1186/s12014-019-9261-1