Chemokine Oligomers and the Impact of Fondaparinux Binding.
Gergo Peter SzekeresDouglas P DyerRebecca Louise MillerKevin PagelPublished in: Journal of the American Society for Mass Spectrometry (2024)
Heparin, a widely used clinical anticoagulant, is generally well-tolerated; however, approximately 1% of patients develop heparin-induced thrombocytopenia (HIT), a serious side effect. While efforts to understand the role of chemokines in HIT development are ongoing, certain aspects remain less studied, such as the stabilization of chemokine oligomers by heparin. Here, we conducted a combined ion mobility-native mass spectrometry study to investigate the stability of chemokine oligomers and their complexes with fondaparinux, a synthetic heparin analog. Collision-induced dissociation and unfolding experiments provided clarity on the specificity and relevance of chemokine oligomers and their fondaparinux complexes with varying stoichiometries, as well as the stabilizing effects of fondaparinux binding.
Keyphrases
- venous thromboembolism
- growth factor
- mass spectrometry
- end stage renal disease
- high glucose
- diabetic rats
- newly diagnosed
- ejection fraction
- chronic kidney disease
- drug induced
- peritoneal dialysis
- prognostic factors
- high resolution
- endothelial cells
- atrial fibrillation
- dna binding
- oxidative stress
- binding protein
- patient reported outcomes
- quality improvement
- high performance liquid chromatography
- ms ms
- structural basis