Grant: Discovery Grants Program - Individual
Université de Moncton
$32,000.00
Exploring the mitochondrial phosphoproteome during metabolic stress
EF 2017-18
Résumé
Mitochondria convert most of the energy contained in nutrients into ATP, which is required to perform all cellular biochemical processes needing energy. Therefore, the mitochondrial metabolism needs to be tightly regulated to maintain survival of cells during metabolic stress. For instance, the mitochondrial ATP production needs to be maintained during low nutrient availability whereas it must be increased during exercise to match the energetic needs of cells. Kinases emerged recently as important regulators of mitochondrial functions. These enzymes change the properties of proteins by adding a phosphate group. Although we know that several kinases can be localized in mitochondria where they can target different proteins, little is known about their importance in the regulation of the mitochondrial metabolism during challenging metabolic conditions. Interestingly, the activity of kinases can be activated by several sub-products of the metabolism which are affected in such conditions. Since mitochondria are key regulators of these metabolites, kinases localized within mitochondria could represent direct messengers to regulate the mitochondrial metabolism during metabolic stress. The proposed research program aims to determine the importance of mitochondrial phosphorylation events in the adjustment of mitochondrial functions in response to metabolic stress . The first objective of this proposal is to determine how mitochondrial levels of key metabolites (reactive oxygen species, calcium and ATP) modulate the mitochondrial phosphoproteome, whereas the second objective is to determine how the mitochondrial phosphoproteome is modulated during fasting and exercise. The mitochondrial proteins targeted by these events will be identified. Then, the generation of mutant proteins mimicking these phosphorylation events will enable to understand the functional impact of these processes on the mitochondrial metabolism. The third objective is to identify the kinases involved in the phosphorylation processes occurring in response to metabolic stress. Globally, this research program will identify new intra-mitochondrial biochemical cascades enabling the adjustment of metabolism in response to challenging metabolic conditions. Most wild animals face persistent metabolic stress. For instance, such animals can stay long periods without eating and/or have to migrate for long distances. Therefore, this research program will eventually identify new molecular mechanisms impacting the adaptation of a given species to its environmental niche. Since defects in mitochondrial functions can lead to different pathologies, including diabetes, cancer and neurodegenerative diseases, this proposed work will be of high interest for the development of new tools indicative of the ?health? status of cells, tissues and entire individuals.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
New Brunswick, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
RGPIN-2015-05880
Name nom
HebertChatelain, Etienne
Department département
Biologie - Biologie
Organization id
73
Institution établissement
Université de Moncton
Province en
New Brunswick
Province fr
Nouveau-Brunswick
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2017
Competition year année de concours
2015
Award amount
32000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5111
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Signal transduction
Research subject fr
Transduction de signal
Partie
3
Nb partie
5
Application title
Exploring the mitochondrial phosphoproteome during metabolic stress
Keyword
NSERC
Application summary
Mitochondria convert most of the energy contained in nutrients into ATP, which is required to perform all cellular biochemical processes needing energy. Therefore, the mitochondrial metabolism needs to be tightly regulated to maintain survival of cells during metabolic stress. For instance, the mitochondrial ATP production needs to be maintained during low nutrient availability whereas it must be increased during exercise to match the energetic needs of cells. Kinases emerged recently as important regulators of mitochondrial functions. These enzymes change the properties of proteins by adding a phosphate group. Although we know that several kinases can be localized in mitochondria where they can target different proteins, little is known about their importance in the regulation of the mitochondrial metabolism during challenging metabolic conditions. Interestingly, the activity of kinases can be activated by several sub-products of the metabolism which are affected in such conditions. Since mitochondria are key regulators of these metabolites, kinases localized within mitochondria could represent direct messengers to regulate the mitochondrial metabolism during metabolic stress. The proposed research program aims to determine the importance of mitochondrial phosphorylation events in the adjustment of mitochondrial functions in response to metabolic stress . The first objective of this proposal is to determine how mitochondrial levels of key metabolites (reactive oxygen species, calcium and ATP) modulate the mitochondrial phosphoproteome, whereas the second objective is to determine how the mitochondrial phosphoproteome is modulated during fasting and exercise. The mitochondrial proteins targeted by these events will be identified. Then, the generation of mutant proteins mimicking these phosphorylation events will enable to understand the functional impact of these processes on the mitochondrial metabolism. The third objective is to identify the kinases involved in the phosphorylation processes occurring in response to metabolic stress. Globally, this research program will identify new intra-mitochondrial biochemical cascades enabling the adjustment of metabolism in response to challenging metabolic conditions. Most wild animals face persistent metabolic stress. For instance, such animals can stay long periods without eating and/or have to migrate for long distances. Therefore, this research program will eventually identify new molecular mechanisms impacting the adaptation of a given species to its environmental niche. Since defects in mitochondrial functions can lead to different pathologies, including diabetes, cancer and neurodegenerative diseases, this proposed work will be of high interest for the development of new tools indicative of the ?health? status of cells, tissues and entire individuals.