Affiliations 

  • 1 Faculty of Medicine, Universiti Sultan Zainal Abidin , Medical Campus , Kuala Terengganu , Malaysia
  • 2 Paediatric department, Hospital Kuala Lumpur (HKL) , Jalan Pahang , Kuala Lumpur , Malaysia
  • 3 Pathology Department, Haematology Unit, Hospital Kuala Lumpur (HKL) , Jalan Pahang , Kuala Lumpur , Malaysia
  • 4 Integrative Pharmacogenomics Institute (iPROMISE), Universiti Teknologi Mara (UiTM) , Bandar Puncak Alam , Selangor State , Malaysia
  • 5 Emergency Department, Rockingham Peel Group, South Metropolitan Health Service , Rockingham , West Australia
  • 6 Jeffery Cheah School of Medicine and Health Sciences, Monash University , Subang Jaya , Selangor State , Malaysia
  • 7 LCMS Platform, Jefferey Cheah School of Medicine and Health Sciences, Monash University Malaysia , Subang Jaya , Selangor State , Malaysia
  • 8 School of Medical Science, Health Campus, Universiti Sains Malaysia (USM) , Kubang Kerian , Kelantan , Malaysia
  • 9 National Doping Control Centre, Mahidol University , Rachathawee , Bangkok , Thailand
  • 10 Institute of Molecular Biosciences, Mahidol University , Salaya Campus , Nakornpathom , Thailand
Hemoglobin, 2019 May;43(3):182-187.
PMID: 31298599 DOI: 10.1080/03630269.2019.1632893

Abstract

This is the first report of quadrupole time-of-flight (Q-TOF) mass spectrometric identification of the hemoglobin (Hb) subunits, α, β, δ and γ peptides, derived from enzymatic-digestion of proteins in the early unknown peaks of the cation exchange chromatography of Hb. The objectives were to identify the unknown high performance liquid chromatography (HPLC) peaks in healthy subjects and in patients with β-thalassemia (β-thal). The results demonstrate the existence of pools of free globin chains in red blood cells (RBCs). The α-, β-, δ- and γ-globin peptides were identified in the unknown HPLC peaks. The quantification and role of the free globin pool in patients with β-thal requires further investigation. Identification of all types of Hb subunits in the retention time (RT) before 1 min. suggests that altered Hbs is the nature of these fast-eluting peaks. Relevancy of thalassemias to the protein-aggregation disorders will require review of the role of free globin in the pathology of the disease.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.