Two-component signalling is a widespread biological phenomenon found primarily in procaryotes but also in eucaryotes. Its abundant representation makes it clear that virtually all phenomena studied in bacteria are either directly or indirectly regulated by at least one two- component system. Furthermore, since it appears that all members within each component family share structural and function homology, there is a unifying theme which has allowed previously unrelated biological phenomena to share findings. This type of informational networking is rare and has accelerated the progress in many two-component systems. For example, results from seemingly diverse areas as osmoregulation (OmpR), sporulation (SpoOA/F) or chemotaxis (CheY) have been compared and used to gain insight into each particular system. Also, new members in the 100+ family of CheY homologs can immediately benefit from the cumulative database. Clearly, there are differences and variations but the basic motif appears to be retained. This proposal is focused primarily on the structure and function of CheY. CheY is in the fortunate position of being the only response regulator for which there is high resolution structural information to combine with extensive genetic and biochemical data. We have both solid-state crystallographic and solution NMR structures of CheY. In collaboration with Dr. F.W. Dahlquist, we propose to continue our efforts in solving the solution NMR structure of the phosphorylated form of CheY and defining the molecular mechanism of activation. In addition, we will further elucidate the sites of protein-protein interaction and the conversion of kinase binding domain to the activated flagellar motor binding domain of CheY. We will also study the enhancement of the phosphatase activity of CheZ when it is bound to CheAS. These ambitious experiments represent a fortuitous combination of events; the development of a biologically important signal transduction system, an overproduced and well characterized response regulator protein, and the newly emerging technical advances in crystallography and NMR spectroscopy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI018985-18
Application #
2886413
Study Section
Special Emphasis Panel (ZRG5-MBC-1 (04))
Program Officer
Heyse, Stephen P
Project Start
1982-04-01
Project End
2000-06-30
Budget Start
1999-04-01
Budget End
2000-06-30
Support Year
18
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
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Shukla, D; Zhu, X Y; Matsumura, P (1998) Flagellar motor-switch binding face of CheY and the biochemical basis of suppression by CheY mutants that compensate for motor-switch defects in Escherichia coli. J Biol Chem 273:23993-9
Pruss, B M (1998) Acetyl phosphate and the phosphorylation of OmpR are involved in the regulation of the cell division rate in Escherichia coli. Arch Microbiol 170:141-6
Halkides, C J; Zhu, X; Phillion, D P et al. (1998) Synthesis and biochemical characterization of an analogue of CheY-phosphate, a signal transduction protein in bacterial chemotaxis. Biochemistry 37:13674-80
Dowd, J P; Matsumura, P (1997) The use of flash photolysis for a high-resolution temporal and spatial analysis of bacterial chemotactic behaviour: CheZ is not always necessary for chemotaxis. Mol Microbiol 25:295-302
Pruss, B M; Matsumura, P (1997) Cell cycle regulation of flagellar genes. J Bacteriol 179:5602-4
Zhu, X; Rebello, J; Matsumura, P et al. (1997) Crystal structures of CheY mutants Y106W and T87I/Y106W. CheY activation correlates with movement of residue 106. J Biol Chem 272:5000-6
Wang, H; Matsumura, P (1997) Phosphorylating and dephosphorylating protein complexes in bacterial chemotaxis. J Bacteriol 179:287-9
Zhu, X; Volz, K; Matsumura, P (1997) The CheZ-binding surface of CheY overlaps the CheA- and FliM-binding surfaces. J Biol Chem 272:23758-64
Wang, H; Matsumura, P (1996) Characterization of the CheAS/CheZ complex: a specific interaction resulting in enhanced dephosphorylating activity on CheY-phosphate. Mol Microbiol 19:695-703

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