The transport of heme by hemopexin to tissues like liver is a specific, membrane receptor-mediated process. As a result, biologically useful iron is conserved, the accumulation of toxic heme is prevented, and the growth of invading microorganisms inhibited. The ultimate aim of our research is to delineate the biochemical mechanisms of heme transport by hemopexin: from initial binding of heme in the circulation, to the specific interaction with the liver plasma membrane receptor, to transfer of heme from hemopexin to membrane components, and finally to the intracellular transport of heme to heme oxygenase. To attain this goal, a basic approach is being taken in which the components of the hemopexin system are being characterized in detail and their inter-relationships examined to determined the mechanisms by which this system carries out its biological role. This proposal focuses on the hemopexin molecule. the hemopexin receptor and the expression of these proteins in cultured cells. The internalization of the heme and the role of the heme-binding membrane protein (MHBP) discovered in this laboratory are the subject of another project and beyond the scope of this proposal.
The specific aims here are: 1. to define the structure-function relationships of hemopexin with special emphasis on the two domains of hemopexin and on the mechanism of the interaction of hemopexin with irs receptor; 2. to use the polyclonal antibodies to the mouse and human receptor now being prepared to determine the molecular properties of the hemopexin receptor and to clone the receptor cDNA from expression vector libraries; 3. to elucidate the mechanisms which regulate the expression of hemopexin and of its receptor in cultured cells with special attention to the roles of heme and iron in this regulation. Most of the tools needed to achieve these aims are in hand including appropriate lambda gt 11 expression vector libraries, cloned hemopexin cDNA, mono and poly-clonal antibodies to hemopexin and appropriate cell lines. The other needed tools, e.g. antibodies to the receptor, are currently being prepared using the experience gained in earlier stages of this research.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK027237-09
Application #
3228230
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1979-12-01
Project End
1990-11-30
Budget Start
1987-12-01
Budget End
1988-11-30
Support Year
9
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Louisiana State University Hsc New Orleans
Department
Type
School of Medicine & Dentistry
DUNS #
782627814
City
New Orleans
State
LA
Country
United States
Zip Code
70112
Wu, M L; Morgan, W T (1995) Thermodynamics of heme-induced conformational changes in hemopexin: role of domain-domain interactions. Protein Sci 4:29-34
Faber, H R; Groom, C R; Baker, H M et al. (1995) 1.8 A crystal structure of the C-terminal domain of rabbit serum haemopexin. Structure 3:551-9
Cox, M C; Le Brun, N; Thomson, A J et al. (1995) MCD, EPR and NMR spectroscopic studies of rabbit hemopexin and its heme binding domain. Biochim Biophys Acta 1253:215-23
Wu, M L; Morgan, W T (1994) Conformational analysis of hemopexin by Fourier-transform infrared and circular dichroism spectroscopy. Proteins 20:185-90
Wu, M L; Morgan, W T (1993) Characterization of hemopexin and its interaction with heme by differential scanning calorimetry and circular dichroism. Biochemistry 32:7216-22
Morgan, W T; Muster, P; Tatum, F et al. (1993) Identification of the histidine residues of hemopexin that coordinate with heme-iron and of a receptor-binding region. J Biol Chem 268:6256-62
Baker, H M; Norris, G E; Morgan, W T et al. (1993) Crystallization of the C-terminal domain of rabbit serum hemopexin. J Mol Biol 229:251-2
Muster, P; Tatum, F; Smith, A et al. (1991) Further characterization of structural determinants of rabbit hemopexin function. J Protein Chem 10:123-8
Smith, A; Farooqui, S M; Morgan, W T (1991) The murine haemopexin receptor. Evidence that the haemopexin-binding site resides on a 20 kDa subunit and that receptor recycling is regulated by protein kinase C. Biochem J 276 ( Pt 2):417-25
Tatum, F; Alam, J; Smith, A et al. (1990) Molecular cloning, nucleotide sequence heterozygosity and regulation of rabbit serum amyloid A cDNA. Nucleic Acids Res 18:7447

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