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LECT 21: REGULATED PROTEIN TURNOVER
Cellular proteins have different stabilities. It is the combination of synthesis and degradation rates that determines the level of a protein in a cell, and changes in either rate can serve as means to regulate a protein’s concentration in the cell. Protein degradation in response to extracellular signals is an important component of some intracellular signaling pathways. Protein degradation is further required to mis-folded or de-folded proteins, which would otherwise be capable of forming insoluble aggregates.
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Machinery for Protein Degradation Within Cells
Cytosolic proteins targeted for degradation are digested in the 26S proteasome, a large multienzymatic structure. Membrane proteins targeted for degradation travel through endosomes to the lysosome, whose lumen contains a collection of proteases. Both targeting processes employ the covalent tagging of proteins with ubiquitin, a small 76 amino acid polypeptide.
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Cbl Terminates Growth Factor Signaling Thru Receptor Ubiquination
EGF EGF EGFR (inactive) EGFR (dimerized, phospho-Y) active POSITIVE SIGNALING SIGNAL TERMINATION Cbl (E3) Several pathways activated for growth or differentiation Internalization, ubiquitination, trafficking to lysosome
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Proteasomal Degradation Can Activate Signaling Pathways:
Transcription Via NFkB Extracellular Signal Proteasome Degradation Ub Ub IkB IKK E3 NFkB Nuclear Transport DNA Binding Transcription Activation
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