The overall goal of our research is a better understanding of biological membrane structure and function, including lipid-protein and protein- protein interaction, and membrane protein folding. Development of powerful biophysical and biochemical methods, especially fluorescence techniques, is of special concern. Specifically, our goal is to understand the behavior of diphtheria toxin and related proteins. Three steps in the entry of toxin into cells are under study. First, how and why the toxin changes from a hydrophilic to hydrophobic state. Second, the conformation of membrane-inserted toxin. Third, how the poisonous A domain of the toxin is released from the membrane and enters the cytoplasm. To characterized these processes the toxin will be examined both in solution and when inserted in model membranes. A variety of methods will be used to analyze toxin structure including chemical labeling, fluorescence, proteolytic, immunological, and calorimetric approaches. Both wild type toxin and mutants containing single Trp and single sulfhydryl groups introduced by site-directed mutagenesis will be studied. This will allow site-specific labeling and determination of the location of defined sites. The behavior of whole toxin and its isolated A domain will be compared in order to define the role of individual domains in the translocation process. The project will also be extended to Pseudomonas exotoxin A, a membrane-penetrating protein that undergoes major conformational changes similar to those in diphtheria toxin. These studies should increase our general knowledge of the processes of membrane insertion and membrane translocation of proteins. They should help in understanding bacterial infection, and by revealing the similarities between toxin and viral entry into cells they should also help in understanding the viral infection process. Finally, they should help in design of therapeutically useful immunotoxins, antibody-toxin hybrids targeted to destroy specific cells (e.g. tumor cells).

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM031986-11
Application #
2176389
Study Section
Physical Biochemistry Study Section (PB)
Project Start
1983-04-01
Project End
1994-11-30
Budget Start
1993-12-01
Budget End
1994-11-30
Support Year
11
Fiscal Year
1994
Total Cost
Indirect Cost
Name
State University New York Stony Brook
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Wang, Jie; London, Erwin (2009) The membrane topography of the diphtheria toxin T domain linked to the a chain reveals a transient transmembrane hairpin and potential translocation mechanisms. Biochemistry 48:10446-56
Lai, Bing; Zhao, Gang; London, Erwin (2008) Behavior of the deeply inserted helices in diphtheria toxin T domain: helices 5, 8, and 9 interact strongly and promote pore formation, while helices 6/7 limit pore formation. Biochemistry 47:4565-74
Fujita, Kentaro; Krishnakumar, Shyam S; Franco, David et al. (2007) Membrane topography of the hydrophobic anchor sequence of poliovirus 3A and 3AB proteins and the functional effect of 3A/3AB membrane association upon RNA replication. Biochemistry 46:5185-99
Buchanan, Susan K; Lukacik, Petra; Grizot, Sylvestre et al. (2007) Structure of colicin I receptor bound to the R-domain of colicin Ia: implications for protein import. EMBO J 26:2594-604
White, Dawn; Musse, Abdiwahab A; Wang, Jie et al. (2006) Toward elucidating the membrane topology of helix two of the colicin E1 channel domain. J Biol Chem 281:32375-84
Wu, Zhengyan; Jakes, Karen S; Samelson-Jones, Ben S et al. (2006) Protein translocation by bacterial toxin channels: a comparison of diphtheria toxin and colicin Ia. Biophys J 91:3249-56
Wang, Jie; Rosconi, Michael P; London, Erwin (2006) Topography of the hydrophilic helices of membrane-inserted diphtheria toxin T domain: TH1-TH3 as a hydrophilic tether. Biochemistry 45:8124-34
Zhao, Gang; London, Erwin (2006) An amino acid ""transmembrane tendency"" scale that approaches the theoretical limit to accuracy for prediction of transmembrane helices: relationship to biological hydrophobicity. Protein Sci 15:1987-2001
Musse, Abdiwahab A; Wang, Jie; Deleon, Gladys P et al. (2006) Scanning the membrane-bound conformation of helix 1 in the colicin E1 channel domain by site-directed fluorescence labeling. J Biol Chem 281:885-95
Zhao, Gang; London, Erwin (2005) Behavior of diphtheria toxin T domain containing substitutions that block normal membrane insertion at Pro345 and Leu307: control of deep membrane insertion and coupling between deep insertion of hydrophobic subdomains. Biochemistry 44:4488-98

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