Second generation low oxygen affinity pegylated hemoglobins as oxygen-carrying plasma expanders
View Patent ↗Provided are hemoglobins having at least two chemical modifications that lower oxygen affinity, hemoglobins chemically modified by the addition of glyceraldehyde-3-phosphate, and hemoglobins having at least two specific chemical modifications. PEGylated versions of these hemoglobins are also provided, as are certain tetraPEGylated and diPEGylated hemoglobins. Methods of modifying a hemoglobin are additionally provided, as are methods of making a hemoglobin. Pharmaceutical compositions and blood substitutes using these hemoglobins are further provided, as are methods of treating a subject using these pharmaceutical compositions and blood substitutes.
1. A method of modifying a hemoglobin, the method comprising introducing at least two chemical modifications to the hemoglobin, wherein each chemical modification by itself results in a hemoglobin with lower oxygen affinity than the same hemoglobin that is unmodified, wherein one of the chemical modifications comprises PEGylating the hemoglobin, wherein the hemoglobin comprises at least one thiol at a Cys-92(β) or a Cys-93(β), wherein the Cys-92(β) or the Cys-93(β) is protected before PEGylation, then deprotected after PEGylation, and wherein the Cys-92(β) or the Cys-93(β) is protected with dithiopyridine and deprotected with Tris(2-carboxyethyl)phosphine (TCEP).
2. The method of claim 1 , wherein one of the chemical modifications is an intramolecular crosslink.
3. The method of claim 2 , wherein the intramolecular crosslink is an α-fumaryl crosslink at Lys-99(α).
4. The method of claim 1 , wherein one of the chemical modifications is an affinity labeling of an effector binding domain.
5. The method of claim 1 , wherein one of the chemical modifications is the introduction of a negative charge at the amino terminal of a β-chain.
6. The method of claim 5 , wherein the introduction of a negative charge is by the addition of glyceraldehyde-3-phosphate in the presence of sodium cyanoborohydride.
7. The method of claim 5 , wherein the introduction of a negative charge is by 2-hydroxy, 3-phospho propylation (HPPr).
8. The method of claim 1 , wherein one chemical modification is by HPPr and another chemical modification is an αα-fumaryl crosslink at Lys-99(α).
9. The method of claim 8 , wherein the αα-fumaryl crosslink is introduced into an HPPr-Hb.
10. A method of modifying a hemoglobin, the method comprising adding glyceraldehyde-3-phosphate to the hemoglobin in the presence of sodium cyanoborohydride, and PEGylating the hemoglobin, wherein the hemoglobin comprises at least one thiol at a Cys-92(β) or a Cys-93(β), wherein the Cys-92(β) or the Cys-93(β) is protected before PEGylation, then deprotected after PEGylation, and wherein the Cys-92(β) or the Cys-93(β) is protected with dithiopyridine and deprotected with Tris(2-carboxyethyl)phosphine (TCEP).
11. A method of modifying a hemoglobin, the method comprising introducing at least two chemical modifications to the hemoglobin, wherein each chemical modification is independently an intramolecular crosslink, an affinity labeling of an effector binding domain, or an introduction of a negative charge at the amino terminal of a β-chain, and PEGylating the hemoglobin, wherein the hemoglobin comprises at least one thiol at a Cys-92(β) or a Cys-93(β), wherein the Cys-92(β) or the Cys-93(β) is protected before PEGylation, then deprotected after PEGylation, and wherein the Cys-92(β) or the Cys-93(β) is protected with dithiopyridine and deprotected with Tris(2-carboxyethyl)phosphine (TCEP).
12. The method of claim 1 , wherein the PEGylation is by reductive alkylation.
13. The method of claim 1 , wherein the PEGylation is by extension arm facilitated maleimide chemistry.
14. The method of claim 12 , wherein the hemoglobin is diPEGylated or tetraPEGylated or hexaPEGylated.
15. A method of making a hemoglobin, the method comprising tetraPEGylating the hemoglobin by extension arm facilitated maleimide chemistry or diPEGylating the hemoglobin by extension arm facilitated maleimide chemistry or hexaPEGylating the hemoglobin by extension arm facilitated maleimide chemistry, wherein the hemoglobin comprises at least one thiol at a Cys-92(β) or Cys-93(β), wherein the Cys-92(β) or the Cys-93(β) is protected before PEGylation, then deprotected after PEGylation, and wherein the Cys-92(β) or the Cys-93(β) is protected with dithiopyridine and deprotected with Tris(2-carboxyethyl)phosphine (TCEP).
16. The method of claim 10 , wherein the PEGylation is by extension arm facilitated maleimide chemistry.
17. The method of claim 11 , wherein the PEGylation is by extension arm facilitated maleimide chemistry.
18. The method of claim 1 , wherein the PEG is maleimido phenyl PEG.
19. The method of claim 1 , wherein the PEG has a molecular weight of 5,000 daltons.