Abstract
The heterotetrameric adaptor complex 1 (AP-1) and the monomeric Golgi-localized, gamma ear-containing, Arf-binding (GGA) proteins are components of clathrin coats associated with the trans-Golgi network and endosomes. The carboxyl-terminal ear domains (or gamma-adaptin ear (GAE) domains) of two gamma-adaptin subunit isoforms of AP-1 and of the GGAs are structurally similar and bind to a common set of accessory proteins. In this study, we have systematically defined a core tetrapeptide motif PsiG(P/D/E)(Psi/L/M) (where Psi is an aromatic residue), which is responsible for the interactions of accessory proteins with GAE domains. The definition of this motif has allowed us to identify novel GAE-binding partners named NECAP and aftiphilin, which also contain clathrin-binding motifs. These findings shed light on the mechanism of accessory protein recruitment to trans-Golgi network and endosomal clathrin coats.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adaptor Protein Complex 1
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Adaptor Protein Complex gamma Subunits / chemistry*
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Adaptor Protein Complex gamma Subunits / metabolism
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Adaptor Proteins, Vesicular Transport*
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Amino Acid Sequence
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Animals
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Binding Sites
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Biotinylation
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Carrier Proteins / chemistry
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Carrier Proteins / metabolism
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Clathrin / metabolism
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Consensus Sequence
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Glutathione Transferase / genetics
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Green Fluorescent Proteins
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Humans
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Luminescent Proteins / genetics
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Mice
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Microscopy, Fluorescence
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Molecular Sequence Data
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Mutagenesis
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Peptide Fragments / chemistry
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Peptide Fragments / metabolism
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Peptide Library
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Recombinant Fusion Proteins
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Saccharomyces cerevisiae
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Structure-Activity Relationship
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Two-Hybrid System Techniques
Substances
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Adaptor Protein Complex 1
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Adaptor Protein Complex gamma Subunits
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Adaptor Proteins, Vesicular Transport
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CLINT1 protein, human
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Carrier Proteins
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Clathrin
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Luminescent Proteins
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Peptide Fragments
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Peptide Library
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Recombinant Fusion Proteins
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SYNRG protein, human
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Green Fluorescent Proteins
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Glutathione Transferase