Rapid communications in mass spectrometry : RCM · 2025
Characterization of N-Terminal Acetylated α-Hemoglobin Stabilizing Protein (AHSP) by Top-Down High-Resolution Mass Spectrometry From Human Preterm Newborns Oral Fluid.
СтатьяНазвание и аннотация: Перевод в очереди
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Iavarone Federica, Tirone Chiara, Fattore Simona, De Tomaso Davide, Menzella Nicoletta, Vento Giovanni, Olianas Alessandra, Manconi Barbara, Cabras Tiziana, Guadalupi Giulia, Contini Cristina, Boroumand Mozhgan, Desiderio Claudia, Muntiu Alexandra, Fiorita Antonella, Fraschini Matteo, Fanos Vassilios, Faa Gavino, Messana Irene, Castagnola Massimo
Аннотация
RATIONALE: Alpha-hemoglobin stabilizing protein (AHSP) is an erythroid-specific protein forming a stable complex with free α-hemoglobin, but not with β-hemoglobin or hemoglobin A (α2β2), thus preventing harmful aggregation of α-hemoglobin during normal erythroid cell development and avoiding its pro-oxidant activity. Although its function has been extensively studied in erythroid cells, its presence in preterm newborns' oral fluid remains unexplored. Given the high susceptibility of preterm infants to hematological disorders, characterizing AHSP in their oral fluid could provide valuable insights into fetal erythropoiesis and its potential role as a biomarker for neonatal anemia and transfusion needs.
METHODS: The primary structure of AHSP was determined by high-resolution top-down proteomic analysis using a nano-HPLC-ESI-MS/MS approach on oral fluid samples from preterm newborns. Specimens were collected non-invasively from infants, promptly treated with formic acid, and analyzed with an Orbitrap-based mass spectrometry platform. The intact protein's molecular mass and fragmentation pattern were assessed to determine its primary structure and post-translational modifications. Statistical analysis was performed to explore correlations between AHSP presence and neonatal clinical parameters, including anemia and transfusion needs.
RESULTS: The experimental monoisotopic molecular mass value [M + H+]1+ at m/z 11744.958 ± 0.3 was inconsistent with the protein sequence reported in the literature, and the MS/MS fragmentation pattern was in agreement with the loss of the N-terminal methionine residue followed by Nα-terminal acetylation, a very common post-translational modification, now recognized as having an important role in modulating protein function, localization and protein stability and turnover. The sporadic samples having detectable amounts of AHSP resulted from preterm newborns with severe anemic status, while all were submitted to iron supplementation.
CONCLUSIONS: Although the data obtained so far cannot be used for quantitative analysis or statistical evaluation, AHSP appears to stand out as a potential early biomarker of neonatal hematological disorders, highlighting a new perspective for future investigations.
METHODS: The primary structure of AHSP was determined by high-resolution top-down proteomic analysis using a nano-HPLC-ESI-MS/MS approach on oral fluid samples from preterm newborns. Specimens were collected non-invasively from infants, promptly treated with formic acid, and analyzed with an Orbitrap-based mass spectrometry platform. The intact protein's molecular mass and fragmentation pattern were assessed to determine its primary structure and post-translational modifications. Statistical analysis was performed to explore correlations between AHSP presence and neonatal clinical parameters, including anemia and transfusion needs.
RESULTS: The experimental monoisotopic molecular mass value [M + H+]1+ at m/z 11744.958 ± 0.3 was inconsistent with the protein sequence reported in the literature, and the MS/MS fragmentation pattern was in agreement with the loss of the N-terminal methionine residue followed by Nα-terminal acetylation, a very common post-translational modification, now recognized as having an important role in modulating protein function, localization and protein stability and turnover. The sporadic samples having detectable amounts of AHSP resulted from preterm newborns with severe anemic status, while all were submitted to iron supplementation.
CONCLUSIONS: Although the data obtained so far cannot be used for quantitative analysis or statistical evaluation, AHSP appears to stand out as a potential early biomarker of neonatal hematological disorders, highlighting a new perspective for future investigations.