Summary
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Targeting of newly synthesized proteins is an integral component
of protein synthesis.
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In prokaryotes, targeting is usually achieved by an N-terminal
signal
sequence of about 20 mostly hydrophobic amino acids.
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In eukaryotes, targeting is more complex due to the large
number of different cellular compartments:
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Nuclear targeting via the nuclear pore using
a nuclear localization signal.
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ER targeting (secretory pathway) via
N-terminal signal sequences using SRPs with subsequent attachment
to the ER,
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Followed by transport to the Golgi complex
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Protein degradation of damaged or obsolete proteins is carried
out
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by lysosomes, vesicles filled with degradating
enzymes
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in a ubiqutin-dependent process by specific proteases in
a large cytosolic complex called the proteasome.
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