X-RAY CRYSTALLOGRAPHY OF ENZYMES INVOLVED IN DRUG METABOLISM, BACTERIAL INFECTIO

点击翻译按钮获取中文摘要

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. The Redinbo group uses the tools of structural, molecular and chemical biology to examine dynamic cellular and systemic processes. We focus on four central areas: 1) Nuclear Receptors in transcriptional control and therapeutic development, 2) enzymes in chemotherapy and chemoprotection, 3) DNA manipulation machinery structure, function and inhibition, and 4) Bacterial pathogenesis. These areas overlap, for example we study DNA relaxases and helicases that catalyze the transfer of bacterial antibiotic resistance genes between bacterial cells; thus impacting area 3 & 4. We study how the nuclear receptor PXR binds to xenobiotic chemicals that are foreign to the human body and promotes their inactivation, including anticancer drugs, thus impacting areas 1 & 2. Our main goals are twofold: to advance the use of structural biology to inform how new therapeutics can be directed against bacterial infection, and to help design strategies to increase the lifetime of useful therapeutic compounds in the human body. The structures we target in this proposal will significantly impact these goals.