Mg2+ chemistry is unique among biological cations, and cells possess novel mechanisms for regulating Mg2+ and facilitating its passage through membranes. This application focuses on the CorA Mg2+ transporter, the primary Mg2+ uptake system for most Eubacteria and Archaea. The crystal structure of CorA from Thermotoga maritima has been determined to 3.9 A resolution. It is a funnel-shaped homopentamer with 2 transmembrane (TM) helices. The extracellular region is composed of only a short conserved loop that connects the 2 TM helices. The channel is composed of 5 helices, 1 from each monomer and appears gated by the side chains of bulky hydrophobic residues within the pore. These helices extend well beyond the membrane through the cytoplasmic domain, forming the funnel inner surface. Outside the funnel, the cytoplasmic neck of the pore is surrounded by a ring of highly conserved positively charged residues. 2 negatively charged helices in the cytoplasmic domain extend back towards the membrane outside the funnel and abut the ring of positive charge. These exterior helices may serve to counteract the positively charged ring, suggesting a gating mechanism. An apparent Mg2+ ion was bound in the cytoplasmic domain between monomers, linking the extended helix from 1 monomer to a set of helices in another. The Mg2+ binding site, conserved in CorA orthologs, may link pore opening to the intracellular concentration of Mg2+.
Aim 1 will continue study of CorA and its mechanism of Mg2+ transport using site directed mutagenesis and transport assays to probe the hypothesized mechanism of transport and gating.
Aim 2 will continue structural work on the T. maritima CorA including determination of an open pore form of CorA and to determine the structure of the soluble domain of S. Typhimurium CorA.
Aim 3 will focus on other members of the large CorA family. Bacterial ZntB has modest sequence identity to CorA but mediates efflux of Zn2+ rather than influx of Mg2+. Eukaryotic Mrs2 proteins mediate Mg2+ influx into mitochondria but have sequence similarity with CorA only in the membrane domain. We propose to test the hypothesis that the structures of ZntB and Mrs2 are identical to that of the CorA Mg2+ transporter by determining the crystal structures of the soluble domains of both transporters. Health relevance. Study of CorA is important because it is a virulence factor in prokaryotes and thus an antibiotic target. In addition, it mediates Mg2+ flux into mitochondria and thus is important in control of Mg2+ homeostasis in eukaryotic cells and possibly in the mitochondrion's role in apoptosis.
| Wan, Qun; Ahmad, Md Faiz; Fairman, James et al. (2011) X-ray crystallography and isothermal titration calorimetry studies of the Salmonella zinc transporter ZntB. Structure 19:700-10 |
| Moomaw, Andrea S; Maguire, Michael E (2010) Cation selectivity by the CorA Mg2+ channel requires a fully hydrated cation. Biochemistry 49:5998-6008 |
| Moomaw, Andrea S; Maguire, Michael E (2008) The unique nature of mg2+ channels. Physiology (Bethesda) 23:275-85 |
| Papp-Wallace, Krisztina M; Nartea, Margaret; Kehres, David G et al. (2008) The CorA Mg2+ channel is required for the virulence of Salmonella enterica serovar typhimurium. J Bacteriol 190:6517-23 |
| Papp-Wallace, Krisztina M; Maguire, Michael E (2008) Regulation of CorA Mg2+ channel function affects the virulence of Salmonella enterica serovar typhimurium. J Bacteriol 190:6509-16 |
| Gunzel, Dorothee; Kucharski, Lisa M; Kehres, David G et al. (2006) The MgtC virulence factor of Salmonella enterica serovar Typhimurium activates Na(+),K(+)-ATPase. J Bacteriol 188:5586-94 |
| Maguire, Michael E (2006) Magnesium transporters: properties, regulation and structure. Front Biosci 11:3149-63 |
| Maguire, Michael E (2006) The structure of CorA: a Mg(2+)-selective channel. Curr Opin Struct Biol 16:432-8 |
| Papp, Krisztina M; Maguire, Michael E (2004) The CorA Mg2+ transporter does not transport Fe2+. J Bacteriol 186:7653-8 |
| Warren, Mary Ann; Kucharski, Lisa M; Veenstra, Alexander et al. (2004) The CorA Mg2+ transporter is a homotetramer. J Bacteriol 186:4605-12 |
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