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Qu'est-ce (qui) est proteasome - définition
![[[Bortezomib]] bound to the core particle in a [[yeast]] proteasome. The bortezomib molecule is in the center colored by atom type ([[carbon]] = pink, [[nitrogen]] = blue, [[oxygen]] = red, [[boron]] = yellow), surrounded by the local protein surface. The blue patch is the catalytic [[threonine]] residue whose activity is blocked by the presence of bortezomib.](https://commons.wikimedia.org/wiki/Special:FilePath/2f16 bortezomib pink.png?width=200 "[[Bortezomib]] bound to the core particle in a [[yeast]] proteasome. The bortezomib molecule is in the center colored by atom type ([[carbon]] = pink, [[nitrogen]] = blue, [[oxygen]] = red, [[boron]] = yellow), surrounded by the local protein surface. The blue patch is the catalytic [[threonine]] residue whose activity is blocked by the presence of bortezomib.")
![Chemical structure of [[bortezomib]] (Boronated form of MG132), a proteasome inhibitor used in [[chemotherapy]] that is particularly effective against [[multiple myeloma]]](https://commons.wikimedia.org/wiki/Special:FilePath/Bortezomib.svg?width=200 "Chemical structure of [[bortezomib]] (Boronated form of MG132), a proteasome inhibitor used in [[chemotherapy]] that is particularly effective against [[multiple myeloma]]")
![E. coli]]''. This complex of [[heat shock protein]]s is thought to resemble the ancestor of the modern proteasome.](https://commons.wikimedia.org/wiki/Special:FilePath/Hslvu ecoli.png?width=200 "E. coli]]''. This complex of [[heat shock protein]]s is thought to resemble the ancestor of the modern proteasome.")
![A cutaway view of the proteasome 20S core particle illustrating the locations of the [[active site]]s. The α subunits are represented as green spheres and the β subunits as protein backbones colored by individual [[polypeptide chain]]. The small pink spheres represent the location of the active-site [[threonine]] residue in each subunit. Light blue chemical structures are the inhibitor [[bortezomib]] bound to the active sites.](https://commons.wikimedia.org/wiki/Special:FilePath/Proteasome cutaway 2.png?width=200 "A cutaway view of the proteasome 20S core particle illustrating the locations of the [[active site]]s. The α subunits are represented as green spheres and the β subunits as protein backbones colored by individual [[polypeptide chain]]. The small pink spheres represent the location of the active-site [[threonine]] residue in each subunit. Light blue chemical structures are the inhibitor [[bortezomib]] bound to the active sites.")
![[[Ribbon diagram]] of [[ubiquitin]], the highly conserved [[protein]] that serves as a molecular tag targeting proteins for degradation by the proteasome](https://commons.wikimedia.org/wiki/Special:FilePath/Ubiquitin cartoon.png?width=200 "[[Ribbon diagram]] of [[ubiquitin]], the highly conserved [[protein]] that serves as a molecular tag targeting proteins for degradation by the proteasome")
![The [[ubiquitin]]ation pathway](https://commons.wikimedia.org/wiki/Special:FilePath/Ubiquitylation.png?width=200 "The [[ubiquitin]]ation pathway")
Wikipédia
Proteasomes are protein complexes which degrade unneeded or damaged proteins by proteolysis, a chemical reaction that breaks peptide bonds. Enzymes that help such reactions are called proteases.
Proteasomes are part of a major mechanism by which cells regulate the concentration of particular proteins and degrade misfolded proteins. Proteins are tagged for degradation with a small protein called ubiquitin. The tagging reaction is catalyzed by enzymes called ubiquitin ligases. Once a protein is tagged with a single ubiquitin molecule, this is a signal to other ligases to attach additional ubiquitin molecules. The result is a polyubiquitin chain that is bound by the proteasome, allowing it to degrade the tagged protein. The degradation process yields peptides of about seven to eight amino acids long, which can then be further degraded into shorter amino acid sequences and used in synthesizing new proteins.
Proteasomes are found inside all eukaryotes and archaea, and in some bacteria. In eukaryotes, proteasomes are located both in the nucleus and in the cytoplasm.
In structure, the proteasome is a cylindrical complex containing a "core" of four stacked rings forming a central pore. Each ring is composed of seven individual proteins. The inner two rings are made of seven β subunits that contain three to seven protease active sites. These sites are located on the interior surface of the rings, so that the target protein must enter the central pore before it is degraded. The outer two rings each contain seven α subunits whose function is to maintain a "gate" through which proteins enter the barrel. These α subunits are controlled by binding to "cap" structures or regulatory particles that recognize polyubiquitin tags attached to protein substrates and initiate the degradation process. The overall system of ubiquitination and proteasomal degradation is known as the ubiquitin–proteasome system.
The proteasomal degradation pathway is essential for many cellular processes, including the cell cycle, the regulation of gene expression, and responses to oxidative stress. The importance of proteolytic degradation inside cells and the role of ubiquitin in proteolytic pathways was acknowledged in the award of the 2004 Nobel Prize in Chemistry to Aaron Ciechanover, Avram Hershko and Irwin Rose.
