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Conjugating Hemoglobin and Albumin by Strain-Promoted Azide- Alkyne Cycloaddition.

Chi LeeHarriet Wenxin ChungRonald Kluger
Published in: Chembiochem : a European journal of chemical biology (2024)
A one-to-one conjugate of cross-linked human hemoglobin and human serum albumin results from a strain-promoted alkyne-azide cycloaddition (SPAAC) of the modified proteins. Additions of a strained alkyne-substituted maleimide to the Cys-34 thiol of human serum albumin and an azide-containing cross-link between the amino groups of each β-unit at Lys-82 of human hemoglobin provide sites for coupling by the SPAAC process. The coupled hemoglobin-albumin conjugate can be readily purified from unreacted hemoglobin. The oxygen binding properties of the two-protein bioconjugate demonstrate oxygen affinity and cooperativity that are suitable for use in an acellular oxygen carrier.
Keyphrases
  • human serum albumin
  • endothelial cells
  • red blood cell
  • induced pluripotent stem cells
  • cancer therapy
  • binding protein
  • molecular docking
  • room temperature
  • protein protein
  • transcription factor
  • ionic liquid