ICS Young Scientist Prize|
Keynote
Deciphering the Cellular Copper Trafficking Mechanism in Order to Develop a New Generation of Antibiotics

Copper`s ability to accept and donate single electrons makes it an ideal redox cofactor, and thus one of the most essential metal ions to the survival of the cell. However, copper ions are also involved in the Fenton reaction and hence capable of driving the generation of deleterious hydroxyl radicals, which are deleterious to the cell. Hence, both prokaryotic systems as well as eukaryotic system have developed a considerable regulation mechanism to maintain negligible copper concentration, in the femtomolar concentration. E.coli cells, in common with the vast majority of bacterial cells, require copper for several important enzymes such as ubiquinole oxidases, Cu,Zn-superoxide dismutases, or cytochrome c oxidase. However, as was mentioned above, copper can be deleterious, making protective mechanisms necessary. Deciphering this regulation mechanism in bacteria, is tremendously important from two specific reasons: one over 70% of the putative cuproproteins identified in prokaryotes have homologs in eukaryotes, and thus resolving the copper cycle in prokaryotic systems will also shed light on the copper cycle in eukaryotic systems. Second, copper has been used throughout much of the human civilization as an antimicrobial agent. In this talk we will shed some light on two important copper regulation systems in E.coli: the copper periplasmic efflux system, CusCFBA, and the Cu(I) metal sensor, gene expression regulation system, CueR. Using Electron Paramagnetic Resonance (EPR) spectroscopy, together with biochemical experiments, cell experiments, and computational methods we will show the essentiality of methionine and lysine residues to the interaction between two proteins in the CusCFBA system and for Cu(I) coordination. We will also present a structural model for the CueR-Cu(I)-DNA complex, shedding light on the transcription mechanism of the CueR protein. Last, we will demonstrate how basic understanding of the function of these systems can assist us in designing new class of antibiotics.