Hemoglobin Tetraners Stabilized with Polyaspirins
- 1 January 1992
- journal article
- research article
- Published by Taylor & Francis in Biomaterials, Artificial Cells and Immobilization Biotechnology
- Vol. 20 (2-4) , 243-252
- https://doi.org/10.3109/10731199209119639
Abstract
Organic acids activated by esterification with 3,5-dibromosalicylate react preferentially either with the B82 lysines or the α99 lysines of hemoglobin. The versatility and site specificity of these polysapirins and the usage of both human and bovine hemoglobins allowed the construction of a family of oxygen carriers with various P50 ranging from 10 to 50 mmHg. These derivatives are obtained in pure homogeneous form by column chromatography. They are stabilized tetramers where the dissociation into dimers is inhibited. The latest addition is Tri-(3,5,dibromosallcyl)-benzenetricarboxylate, which crosslinks both human and bovine hemoglobin across the B subunits, decreasing the oxygen affinity of both proteins. The crosslinked hemoglobins have a normal Bohr effect, more expanded in the alkaline region, and are sensitive to chlorides but not to polyphosphates. Solutions of stabilized tetramers, infused into rats or cats up to 25–50% blood replacement, do not produce altered renal and cardiac function. In the cat isovolemic hemodilution increases cerebral flow in controls treated with albumin solutions, when an oxygen carier is used the cerbral flow remains normal.Keywords
This publication has 5 references indexed in Scilit:
- Bovine hemoglobin pseudo‐crosslinked with mono(3,5‐dibromosalicyl)‐fumarateEuropean Journal of Biochemistry, 1990
- Pseudo Cross-link of Human Hemoglobin with Mono- (3,5-dibromosalicyl)fumarateJournal of Biological Chemistry, 1989
- Bovine hemoglobin as a potential source of hemoglobin-based oxygen carriers: crosslinking with bis(2,3-dibromosalycyl)fumarateBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1986
- Isolation and characterization of a new hemoglobin derivative cross-linked between the alpha chains (lysine 99 alpha 1----lysine 99 alpha 2).Journal of Biological Chemistry, 1986
- Development of antisickling compounds that chemically modify hemoglobin S specifically within the 2,3-diphosphoglycerate binding siteJournal of Molecular Biology, 1980