Oxygen binding to Octolasium complanatum erythrocruorin. Modulation of homo- and heterotropic interactions by cations
- PMID: 6502714
- DOI: 10.1016/0022-2836(84)90163-3
Oxygen binding to Octolasium complanatum erythrocruorin. Modulation of homo- and heterotropic interactions by cations
Abstract
The functional properties of erythrocruorin from Octolasium complanatum (a common earthworm of Central Italy) have been characterized in great detail. Special attention has been given to the reciprocal effects of the various ligands, namely oxygen, cations and protons. The data obtained under a variety of experimental conditions bring out the dominant role played by cations in the modulation of both homotropic and heterotropic interactions. In this respect, the most interesting observation concerns the unusual interplay between protons and cations that occurs in this erythrocruorin, the first respiratory pigment in which the Bohr effect is due totally to the O2-linked binding of an allosteric effector. The oxygen binding data collected under the various experimental conditions have been analyzed in terms of a modified two-state model, which takes into account the fact that allosteric effectors may also influence the ligand binding properties of the state that they stabilize. The analysis shows that the number of interacting sites necessary for the observed co-operativity in O2 binding is much smaller than the number of heme groups carried by the whole molecule, in accordance with previous findings on hemocyanins, the other class of giant respiratory pigments. Moreover, the analysis indicates that the dimensions of these "functional constellations" are under the control of allosteric effectors.
Similar articles
-
Assembly of erythrocruorin from the earthworm Octolasium complanatum.J Mol Biol. 1984 Feb 5;172(4):545-58. doi: 10.1016/s0022-2836(84)80022-4. J Mol Biol. 1984. PMID: 6694217
-
Amphitrite ornata erythrocruorin. II. Molecular controls of function.Biochim Biophys Acta. 1981 Aug 28;670(1):84-92. doi: 10.1016/0005-2795(81)90052-0. Biochim Biophys Acta. 1981. PMID: 7272332
-
Studies on erythrocruorin. VII. Reconstitution of earthworm erythrocruorin from the apoprotein.Biochim Biophys Acta. 1978 Jul 21;535(1):150-9. doi: 10.1016/0005-2795(78)90041-7. Biochim Biophys Acta. 1978. PMID: 27229
-
Non-Allosteric Cooperativity in Hemoglobin.Curr Protein Pept Sci. 2018;19(6):573-588. doi: 10.2174/1389203718666171030103310. Curr Protein Pept Sci. 2018. PMID: 29086690 Review.
-
Tertiary and quaternary effects in the allosteric regulation of animal hemoglobins.Biochim Biophys Acta. 2013 Sep;1834(9):1860-72. doi: 10.1016/j.bbapap.2013.03.013. Epub 2013 Mar 20. Biochim Biophys Acta. 2013. PMID: 23523886 Review.
Cited by
-
Principles in the assembly of annelid erythrocruorins.Biophys J. 1986 Jan;49(1):177-89. doi: 10.1016/S0006-3495(86)83633-5. Biophys J. 1986. PMID: 3955169 Free PMC article.
-
Effect of heavy metal exposure on blood haemoglobin concentration and methemoglobin percentage in Lumbricus terrestris.Ecotoxicology. 2011 Jun;20(4):847-54. doi: 10.1007/s10646-011-0641-1. Epub 2011 Mar 22. Ecotoxicology. 2011. PMID: 21424722
-
Structural hierarchy in erythrocruorin, the giant respiratory assemblage of annelids.Proc Natl Acad Sci U S A. 2000 Jun 20;97(13):7107-11. doi: 10.1073/pnas.97.13.7107. Proc Natl Acad Sci U S A. 2000. PMID: 10860978 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources