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Clathrin-mediated endocytosis involves the assembly of a network of proteins that select cargo, modify membrane shape and drive invagination, vesicle scission and uncoating. This network is initially assembled around adaptor protein (AP) appendage domains, which are protein interaction hubs. Using crystallography, we show that FxDxF and WVxF peptide motifs from synaptojanin bind to distinct subdomains on alpha-appendages, called 'top' and 'side' sites. Appendages use both these sites to interact with their binding partners in vitro and in vivo. Occupation of both sites simultaneously results in high-affinity reversible interactions with lone appendages (e.g. eps15 and epsin1). Proteins with multiple copies of only one type of motif bind multiple appendages and so will aid adaptor clustering. These clustered alpha(appendage)-hubs have altered properties where they can sample many different binding partners, which in turn can interact with each other and indirectly with clathrin. In the final coated vesicle, most appendage binding partners are absent and thus the functional status of the appendage domain as an interaction hub is temporal and transitory giving directionality to vesicle assembly.

Original publication

DOI

10.1038/sj.emboj.7600445

Type

Journal article

Journal

EMBO J

Publication Date

10/11/2004

Volume

23

Pages

4371 - 4383

Keywords

Adaptor Protein Complex 2, Amino Acid Motifs, Animals, Binding Sites, COS Cells, Cercopithecus aethiops, Clathrin, Clathrin-Coated Vesicles, Crystallography, X-Ray, Endocytosis, Enzyme Inhibitors, Ligands, Mass Spectrometry, Models, Biological, Models, Molecular, Mutagenesis, Site-Directed, Nerve Tissue Proteins, Phosphoric Monoester Hydrolases, Protein Binding, Protein Structure, Tertiary, Proteomics, Rats, Water