The objective of the current proposal is to identify and characterize at a functional and structural level the proteins involved in heme transport in bacterial pathogens. Pathogenic bacteria require iron for their survival and growth and the ability to acquire this element is linked in part to their virulence. The major source of iron within the body is complexed in heme and heme-containing proteins. Pathogenic bacteria have developed sophisticated mechanisms by which they acquire iron from the hosts heme and hemeproteins. The current increase in the occurrence of antibiotic-resistant strains has created a need to develop alternative strategies to target such pathogens. Structural and functional characterization of proteins involved in heme transport and storage should make it possible to develop specific inhibitors. The expression and purification of the outer-membrane heme receptor (HutA) and periplasmic heme-binding protein (ShuT), will allow biochemical characterization of the heme transport proteins in gram-negative pathogens. The study will be directed towards two specific goals: first, the nature of heme binding to the receptor and transport proteins, and second, the mechanism of heme uptake. Site-directed mutagenesis together with physical techniques such as optical absorption, fluorescence, MCD and resonance Raman spectrophotometry will provide information on the structural features required for heme-binding and transport. The substrate-specificity of the outer-membrane receptor (HutA) and the periplasmic binding protein (ShuT) will be determined with substituted porphyrins, with the premise that such data may provide templates for the development of small molecule inhibitors. The expression of HutA in a heme deficient strain of E. coli allows us to directly monitor heme uptake as a function of cell viability and provides a direct method of determining heme transport in site-directed mutagenesis studies. In addition the coexpression of a bacterial heme oxygenase with the HutA receptor will be developed as a rapid colorimetric screen for future site-directed mutagenesis and inhibitor screening. The redox nature of heme transport will also be investigated with redox inactive non-iron metalloporphyrins such as Co and Zn-protoporphyrin IX. Once an understanding of the mechanism of heme transport in bacterial pathogens has been established the stage will be set for future design of selective inhibitors of heme transport.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI048551-03
Application #
6632426
Study Section
Metallobiochemistry Study Section (BMT)
Program Officer
Van de Verg, Lillian L
Project Start
2001-06-01
Project End
2006-04-30
Budget Start
2003-05-01
Budget End
2004-04-30
Support Year
3
Fiscal Year
2003
Total Cost
$222,750
Indirect Cost
Name
University of Maryland Baltimore
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
188435911
City
Baltimore
State
MD
Country
United States
Zip Code
21201
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Zeng, Yuhong; Caignan, Gregori A; Bunce, Richard A et al. (2005) Azide-inhibited bacterial heme oxygenases exhibit an S = 3/2 (dxz,dyz)3(dxy)1(dz2)1 spin state: mechanistic implications for heme oxidation. J Am Chem Soc 127:9794-807
Eakanunkul, Suntara; Lukat-Rodgers, Gudrun S; Sumithran, Suganya et al. (2005) Characterization of the periplasmic heme-binding protein shut from the heme uptake system of Shigella dysenteriae. Biochemistry 44:13179-91
Wyckoff, Elizabeth E; Schmitt, Michael; Wilks, Angela et al. (2004) HutZ is required for efficient heme utilization in Vibrio cholerae. J Bacteriol 186:4142-51

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