We are interested in the understanding protein-ligand interactions and the microevolutionary processes that permit and promote changes at the protein-ligand interface. To explore these issues, we are studying the Phd repressor/antitoxin and selected homologs. Phd is a small 73 amino acid protein with multiple macromolecular ligands. Phd dimerizes, binds to operator DNA, binds to the Doc toxin, and engages in an additional contact with Doc that mediates the cooperative interactions between adjacent Phd dimers and thus enhances repression. All four of these protein-ligand interactions contribute to the specificity and affinity of the repressive complex.
The specific aims of the current proposals are: 1. To identify the key amino acid determinants for all four protein-ligand interactions. 2. To analyze all four interactions in vitro using wild type and select Phd variants. 3. To determine the topology of the repressive complex. We will use biochemical and genetic methods to quantitatively analyze these four protein-ligand interactions. By testing mutant proteins for multiple activities, we will be able to determine whether the effects of the mutation are local (affecting a single activity of Phd) or global (affecting multiple activities of Phd) and we will be able to determine how one interaction affects another interaction. The long-term objective of this research is to understand protein-ligand interactions well enough to recognize ligand binding domains, match proteins to their preferred ligands, design proteins to bind specific ligands and design ligands to bind specific proteins. A superior understanding of protein-ligand interactions will assist in the rational design of drugs (ligands) that interact with specific protein targets (agents of disease). The proposed research will contribute to the understanding of protein-ligand interactions and a superior understanding of protein-ligand interactions will enable us to design ligands (drugs) that bind specific proteins (viral or microbial or human) that produce human disease. The proposed research will contribute also to the understanding of plasmid addiction elements. These self-selecting sib-killing plasmid addiction elements may have diverse applications in the attenuation of bacteria for vaccine production, in enhancing and prolonging the action of antibiotics and in the modification or elimination of plasmid-borne virulence determinants. ? ? ?
The proposed research will contribute to the understanding of Toxin-Antitoxin systems. Thesesystems modulate the clinical action of antibiotics and may have diverse applications in theattenuation of bacteria for vaccine production and in the modification or elimination ofplasmidborne virulence determinants.
| Garcia-Pino, Abel; Balasubramanian, Sreeram; Wyns, Lode et al. (2010) Allostery and intrinsic disorder mediate transcription regulation by conditional cooperativity. Cell 142:101-11 |
| Garcia-Pino, Abel; Christensen-Dalsgaard, Mikkel; Wyns, Lode et al. (2008) Doc of prophage P1 is inhibited by its antitoxin partner Phd through fold complementation. J Biol Chem 283:30821-7 |
| McKinley, James Estle; Magnuson, Roy David (2005) Characterization of the Phd repressor-antitoxin boundary. J Bacteriol 187:765-70 |
| Zhao, Xueyan; Magnuson, Roy David (2005) Percolation of the phd repressor-operator interface. J Bacteriol 187:1901-12 |
| Smith, Jeremy Allen; Magnuson, Roy David (2004) Modular organization of the Phd repressor/antitoxin protein. J Bacteriol 186:2692-8 |
