Receptors that mediate E. coli chemotaxis are paradigms for a large family of bacterial chemoreceptors and a larger family of prokaryotic and eukaryotic receptors. This proposal focuses on functional mechanisms in these receptors, specifically the relation of oligomeric organization to functional activity, the multiple interactions that control adaptational modification, and functional interactions among heterologous receptors. This focus is consistent with the NIGMS mission of basic research that increases understanding of life processes and lays the foundation for medical advances. Our work involves biochemical, genetic, biophysical and structural approaches plus collaborations with prominent biophysicists, biochemists and modelers. An emerging theme in biological molecular mechanisms is the importance of higher order interactions among proteins and complexes. Such interactions are central for bacterial chemotaxis. We propose to investigate the relation between receptor interactions and function by controlling in vitro the number of potentially interacting homodimers, the smallest unit of functional receptor structure. This control will be accomplished by isolating single or a small number of homodimers in Nanodiscs, water-soluble plugs of lipid bilayer surrounded by a protein annulus, a procedure we developed in a recent study. We will define the functional properties of isolated homodimers, providing a foundation for understanding functional consequences of higher order interactions. We will characterize the minimal receptor unit that activates the chemotaxis kinase, a unit our initial studies implied is 2-3 dimers. The results will define the core unit of the ternary signaling complex and identify features that require higher interactions. Given the potential of Nanodisc technology for studying chemoreceptors and other membrane proteins that form higher oligomers, we will optimize and characterize receptor-Nanodisc preparations. Receptor covalent modifications that mediate sensory adaptation are crucial for effective chemotaxis. They are controlled by multiple receptor-enzyme interactions in complex feedback loops. We will study these interactions using steady-state and transient-state kinetics, biochemical probes and mathematical plus structural modeling. A crucial interaction involves a pentapeptide connected to the receptor body by a polypeptide linker. The linker is required for effective adaptational modification. We will investigate the functional roles and postulated flexible nature of this linker by mutagenic manipulation, molecular modeling combined with experimental tests and EPR spectroscopy. We will characterize interactions among heterologous receptors using in vitro systems for adaptational assistance and for controlling the extent of influences on signaling among heterologous receptors. This research will increase our understanding of how interactions of individual molecules create complex functions. Similar phenomena, present in many life processes, are relevant to heath and disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM029963-28
Application #
7791334
Study Section
Special Emphasis Panel (ZRG1-IDM-A (02))
Program Officer
Gindhart, Joseph G
Project Start
1982-04-01
Project End
2012-03-31
Budget Start
2010-04-01
Budget End
2012-03-31
Support Year
28
Fiscal Year
2010
Total Cost
$521,774
Indirect Cost
Name
University of Missouri-Columbia
Department
Biochemistry
Type
Schools of Medicine
DUNS #
153890272
City
Columbia
State
MO
Country
United States
Zip Code
65211
Bartelli, Nicholas L; Hazelbauer, Gerald L (2016) Bacterial Chemoreceptor Dynamics: Helical Stability in the Cytoplasmic Domain Varies with Functional Segment and Adaptational Modification. J Mol Biol 428:3789-804
Parkinson, John S; Hazelbauer, Gerald L; Falke, Joseph J (2015) Signaling and sensory adaptation in Escherichia coli chemoreceptors: 2015 update. Trends Microbiol 23:257-66
Bartelli, Nicholas L; Hazelbauer, Gerald L (2015) Differential backbone dynamics of companion helices in the extended helical coiled-coil domain of a bacterial chemoreceptor. Protein Sci 24:1764-76
Li, Mingshan; Hazelbauer, Gerald L (2014) Selective allosteric coupling in core chemotaxis signaling complexes. Proc Natl Acad Sci U S A 111:15940-5
Amin, Divya N; Hazelbauer, Gerald L (2012) Influence of membrane lipid composition on a transmembrane bacterial chemoreceptor. J Biol Chem 287:41697-705
Hazelbauer, Gerald L (2012) Bacterial chemotaxis: the early years of molecular studies. Annu Rev Microbiol 66:285-303
Li, Mingshan; Hazelbauer, Gerald L (2011) Core unit of chemotaxis signaling complexes. Proc Natl Acad Sci U S A 108:9390-5
Li, Mingshan; Khursigara, Cezar M; Subramaniam, Sriram et al. (2011) Chemotaxis kinase CheA is activated by three neighbouring chemoreceptor dimers as effectively as by receptor clusters. Mol Microbiol 79:677-85
Bartelli, Nicholas L; Hazelbauer, Gerald L (2011) Direct evidence that the carboxyl-terminal sequence of a bacterial chemoreceptor is an unstructured linker and enzyme tether. Protein Sci 20:1856-66
Hazelbauer, Gerald L; Lai, Wing-Cheung (2010) Bacterial chemoreceptors: providing enhanced features to two-component signaling. Curr Opin Microbiol 13:124-32

Showing the most recent 10 out of 64 publications