Cel Background: AAA+ proteases are ubiquitous molecular machines that execute regulated protein degradation in cells. Their activity is necessary for regulation of many cellular processes, as well as to clear the cell of misfolded, potentially harmful proteins. Failure to combat protein unfolding in unicellular organisms often leads to reduced viability, and in humans, accumulation of misfolded proteins may result in prion diseases, cancer and neurodegenerative disorders. Conserved in bacteria and eukaryotic organelles, the major enzyme responsible for degrading damaged proteins is a hexameric AAA+ protease known as Lon. Despite its central role in most living organisms, the mechanism of substrate degradation by this protease is poorly understood. Objectives & Work Plan: To reveal the detailed molecular mechanism of protein degradation by Lon and related AAA+ proteases by studying the Lon protease of Escherichia coli as a model system. The research will exploit the fact that Lon is the only AAA+ protease for which a natural protein inhibitor – PinA, a T4-bacteriophage protein – is known. Genetic screens will be conducted for the isolation of Lon mutants with improved mechanistic properties that result in faster substrate processing, and for active mutants that are resistant to PinA inhibition (aim 1). To obtain insight into the mechanistic properties of the mutants, biochemical characterization will be carried out using native and unfolded protein substrates, a wide variety of peptide substrates, and sensitive assays for the detection of binding and degradation (aim 2). To solve the 3D structure of Lon, primary crystallization screens will be set-up to optimize the crystallization conditions so as to obtain crystals that diffract at high resolution (aim 3). Relevance to Work Programme: The reintegration grant will aid me to establish an independent laboratory conducting top-level protein research and thereby to obtain a permanent position in university in the ERA. Dziedzina nauki natural sciencesbiological sciencesmicrobiologybacteriologymedical and health sciencesclinical medicineoncologynatural sciencesbiological sciencesbiochemistrybiomoleculesproteinsenzymes Program(-y) FP7-PEOPLE - Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) Temat(-y) FP7-PEOPLE-2009-RG - Marie Curie Action: "Reintegration Grants" Zaproszenie do składania wniosków FP7-PEOPLE-2009-RG Zobacz inne projekty w ramach tego zaproszenia System finansowania MC-IRG - International Re-integration Grants (IRG) Koordynator BEN-GURION UNIVERSITY OF THE NEGEV Wkład UE € 100 000,00 Adres . 84105 Beer Sheva Izrael Zobacz na mapie Rodzaj działalności Higher or Secondary Education Establishments Kontakt administracyjny Daphna Tripto (Ms.) Linki Kontakt z organizacją Opens in new window Strona internetowa Opens in new window Koszt całkowity Brak danych