Under nitroxidative stress, a minor fraction of cytochrome c can be modified by tyrosine nitration. Here we analyze the specific effect of nitration of tyrosines 46 and 48 on the dual role of cytochrome c in cell survival and cell death. Our findings reveal that nitration of these two solvent-exposed residues has a negligible effect on the rate of electron transfer from cytochrome c to cytochrome c oxidase, but impairs the ability of the heme protein to activate caspase-9 by assembling a non-functional apoptosome. It seems that cytochrome c nitration under cellular stress counteracts apoptosis in light of the small amount of modified protein. We conclude that other changes such as increased peroxidase activity prevail and allow the executio...
AbstractApoptotic cell death can occur by two different pathways. Type 1 is initiated by the activat...
AbstractRecent progress in studies on apoptosis has revealed that cytochrome c is a pro-apoptotic fa...
Native cytochrome c (cyt c) has a compact tertiary structure with a hexacoordinated heme iron and fu...
AbstractUnder nitroxidative stress, a minor fraction of cytochrome c can be modified by tyrosine nit...
Here we analyze the specific effect of nitration of tyrosines 46 and 48 on the dual role of cytochro...
Tyrosine nitration is one of the most common post-transcriptional modifications of proteins, so affe...
AbstractTyrosine nitration is one of the most common post-transcriptional modifications of proteins,...
AbstractThe Reactive Nitrogen and Oxygen Species (the so-called RNOS), which are well-known radicals...
AbstractCytochrome c, released from mitochondria into the cytosol, triggers formation of the apoptos...
Cytochrome c delicately tilts the balance between cell life (respiration) and cell death (apoptosis)...
Respiratory cytochrome c has been found to be phosphorylated at tyrosine 97 in the postischemic brai...
A further function of cytochrome c (cyt c), beyond respiration, is realized outside mitochondria in ...
Since the first description of apoptosis four decades ago, great efforts have been made to elucidate...
Regulation of mitochondrial activity allows cells to adapt to changing conditions and to control oxi...
Cytochrome c released from mitochondria into the cytoplasm plays a critical role in many forms of ap...
AbstractApoptotic cell death can occur by two different pathways. Type 1 is initiated by the activat...
AbstractRecent progress in studies on apoptosis has revealed that cytochrome c is a pro-apoptotic fa...
Native cytochrome c (cyt c) has a compact tertiary structure with a hexacoordinated heme iron and fu...
AbstractUnder nitroxidative stress, a minor fraction of cytochrome c can be modified by tyrosine nit...
Here we analyze the specific effect of nitration of tyrosines 46 and 48 on the dual role of cytochro...
Tyrosine nitration is one of the most common post-transcriptional modifications of proteins, so affe...
AbstractTyrosine nitration is one of the most common post-transcriptional modifications of proteins,...
AbstractThe Reactive Nitrogen and Oxygen Species (the so-called RNOS), which are well-known radicals...
AbstractCytochrome c, released from mitochondria into the cytosol, triggers formation of the apoptos...
Cytochrome c delicately tilts the balance between cell life (respiration) and cell death (apoptosis)...
Respiratory cytochrome c has been found to be phosphorylated at tyrosine 97 in the postischemic brai...
A further function of cytochrome c (cyt c), beyond respiration, is realized outside mitochondria in ...
Since the first description of apoptosis four decades ago, great efforts have been made to elucidate...
Regulation of mitochondrial activity allows cells to adapt to changing conditions and to control oxi...
Cytochrome c released from mitochondria into the cytoplasm plays a critical role in many forms of ap...
AbstractApoptotic cell death can occur by two different pathways. Type 1 is initiated by the activat...
AbstractRecent progress in studies on apoptosis has revealed that cytochrome c is a pro-apoptotic fa...
Native cytochrome c (cyt c) has a compact tertiary structure with a hexacoordinated heme iron and fu...