
pmid: 7569928
Tyrosine-based signals within the cytoplasmic domain of integral membrane proteins mediate clathrin-dependent protein sorting in the endocytic and secretory pathways. A yeast two-hybrid system was used to identify proteins that bind to tyrosine-based signals. The medium chains (μ 1 and μ 2 ) of two clathrin-associated protein complexes (AP-1 and AP-2, respectively) specifically interacted with tyrosine-based signals of several integral membrane proteins. The interaction was confirmed by in vitro binding assays. Thus, it is likely that the medium chains serve as signal-binding components of the clathrin-dependent sorting machinery.
Recombinant Fusion Proteins, Cell Membrane, Molecular Sequence Data, Golgi Apparatus, Membrane Proteins, Nerve Tissue Proteins, Saccharomyces cerevisiae, Protein Sorting Signals, Phosphoproteins, Clathrin, Adaptor Proteins, Vesicular Transport, Transformation, Genetic, Tyrosine, Amino Acid Sequence, Cloning, Molecular, Lysosomes, Glutathione Transferase
Recombinant Fusion Proteins, Cell Membrane, Molecular Sequence Data, Golgi Apparatus, Membrane Proteins, Nerve Tissue Proteins, Saccharomyces cerevisiae, Protein Sorting Signals, Phosphoproteins, Clathrin, Adaptor Proteins, Vesicular Transport, Transformation, Genetic, Tyrosine, Amino Acid Sequence, Cloning, Molecular, Lysosomes, Glutathione Transferase
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