Apoptosome: Difference between revisions
CSV import |
CSV import |
||
| Line 5: | Line 5: | ||
File:177-Apoptosomes_apoptosomes.png|Apoptosomes | File:177-Apoptosomes_apoptosomes.png|Apoptosomes | ||
</gallery> | </gallery> | ||
== Apoptosome == | |||
The '''apoptosome''' is a large quaternary protein structure formed in the process of [[apoptosis]], or programmed cell death. It plays a crucial role in the intrinsic pathway of apoptosis by activating [[caspase]] enzymes, which are responsible for the execution phase of cell death. | |||
=== Structure === | |||
The apoptosome is typically composed of several molecules of [[Apoptotic protease activating factor 1|Apaf-1]], [[cytochrome c]], and [[adenosine triphosphate|ATP]] or [[deoxyadenosine triphosphate|dATP]]. In humans, the apoptosome is a heptameric complex, meaning it consists of seven Apaf-1 molecules. Each Apaf-1 molecule contains several domains, including a caspase recruitment domain (CARD), a nucleotide-binding oligomerization domain (NOD), and a series of WD40 repeats. | |||
=== Formation === | |||
The formation of the apoptosome is initiated by the release of cytochrome c from the [[mitochondrion|mitochondria]] into the [[cytosol]]. This release is often triggered by cellular stress or damage signals. Once in the cytosol, cytochrome c binds to Apaf-1, causing a conformational change that allows Apaf-1 to bind ATP or dATP. This binding promotes the oligomerization of Apaf-1 into the heptameric apoptosome structure. | |||
=== Function === | |||
The primary function of the apoptosome is to activate [[caspase-9]], an initiator caspase. The CARD domain of Apaf-1 interacts with the CARD domain of procaspase-9, facilitating its recruitment to the apoptosome. Once bound, procaspase-9 undergoes autocatalytic cleavage to become active caspase-9. Active caspase-9 then cleaves and activates downstream effector caspases, such as caspase-3 and caspase-7, which execute the cell death program by cleaving various cellular substrates. | |||
=== Regulation === | |||
The activity of the apoptosome is tightly regulated by several factors. [[Inhibitor of apoptosis proteins|IAPs]] can bind to and inhibit active caspases, thus preventing apoptosis. Additionally, the [[Bcl-2 family]] of proteins regulates the release of cytochrome c from the mitochondria, thereby controlling apoptosome formation. Pro-apoptotic members of the Bcl-2 family, such as [[Bax]] and [[Bak]], promote cytochrome c release, while anti-apoptotic members, such as [[Bcl-2]] and [[Bcl-xL]], inhibit it. | |||
== Related pages == | |||
* [[Apoptosis]] | |||
* [[Caspase]] | |||
* [[Cytochrome c]] | |||
* [[Mitochondrion]] | |||
* [[Bcl-2 family]] | |||
{{Apoptosis}} | |||
[[Category:Apoptosis]] | |||
[[Category:Protein complexes]] | |||
Latest revision as of 00:42, 19 February 2025
-
Human apoptosome CARD complex
-
Apoptosome atomic model
-
Apoptosome surface rendering
-
Apoptosomes
Apoptosome[edit]
The apoptosome is a large quaternary protein structure formed in the process of apoptosis, or programmed cell death. It plays a crucial role in the intrinsic pathway of apoptosis by activating caspase enzymes, which are responsible for the execution phase of cell death.
Structure[edit]
The apoptosome is typically composed of several molecules of Apaf-1, cytochrome c, and ATP or dATP. In humans, the apoptosome is a heptameric complex, meaning it consists of seven Apaf-1 molecules. Each Apaf-1 molecule contains several domains, including a caspase recruitment domain (CARD), a nucleotide-binding oligomerization domain (NOD), and a series of WD40 repeats.
Formation[edit]
The formation of the apoptosome is initiated by the release of cytochrome c from the mitochondria into the cytosol. This release is often triggered by cellular stress or damage signals. Once in the cytosol, cytochrome c binds to Apaf-1, causing a conformational change that allows Apaf-1 to bind ATP or dATP. This binding promotes the oligomerization of Apaf-1 into the heptameric apoptosome structure.
Function[edit]
The primary function of the apoptosome is to activate caspase-9, an initiator caspase. The CARD domain of Apaf-1 interacts with the CARD domain of procaspase-9, facilitating its recruitment to the apoptosome. Once bound, procaspase-9 undergoes autocatalytic cleavage to become active caspase-9. Active caspase-9 then cleaves and activates downstream effector caspases, such as caspase-3 and caspase-7, which execute the cell death program by cleaving various cellular substrates.
Regulation[edit]
The activity of the apoptosome is tightly regulated by several factors. IAPs can bind to and inhibit active caspases, thus preventing apoptosis. Additionally, the Bcl-2 family of proteins regulates the release of cytochrome c from the mitochondria, thereby controlling apoptosome formation. Pro-apoptotic members of the Bcl-2 family, such as Bax and Bak, promote cytochrome c release, while anti-apoptotic members, such as Bcl-2 and Bcl-xL, inhibit it.
Related pages[edit]
| Apoptosis | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|
This apoptosis-related article is a stub.
|