Evidence for CALM in directing VAMP2 trafficking.

Abstract

Clathrin assembly lymphoid myeloid leukemia protein (CALM) is a clathrin assembly protein with a domain structure similar to the neuron-specific assembly protein AP180. We have previously found that CALM is expressed in neurons and present in synapses. We now report that CALM has a neuron-related function: it facilitates the endocytosis of the synaptic vesicle protein VAMP2 from the plasma membrane. Overexpression of CALM leads to the reduction of cell surface VAMP2, whereas knockdown of CALM by RNA interference results in the accumulation of surface VAMP2. The AP180 N-terminal homology (ANTH) domain of CALM is required for its effect on VAMP2 trafficking, and the ANTH domain itself acts as a dominant-negative mutant. Thus, our results reveal a role for CALM in directing VAMP2 trafficking during endocytosis.

• Authors: Asaff Harel, Fangbai Wu, Mark P Mattson, Christa M Morris, Pamela J Yao
• Journal: Traffic (Copenhagen, Denmark) (Traffic) Vol. 9 Issue 3 Pg. 417-29 (Mar 2008) ISSN: 1398-9219 [Print] England
• PMID: 18182011 (Publication Type: Journal Article, Research Support, N.I.H., Intramural)

Chemical References

• Monomeric Clathrin Assembly Proteins
• PICALM protein, human
• RNA, Small Interfering
• Recombinant Proteins
• Transferrin
• VAMP2 protein, human
• Vesicle-Associated Membrane Protein 2

Topics

• Animals
• Cell Line
• Cell Membrane (metabolism)
• Endocytosis
• Humans
• Monomeric Clathrin Assembly Proteins (antagonists & inhibitors, chemistry, genetics, metabolism)
• Mutagenesis, Site-Directed
• PC12 Cells
• Protein Structure, Tertiary
• Protein Transport
• RNA Interference
• RNA, Small Interfering (genetics)
• Rats
• Recombinant Proteins (genetics, metabolism)
• Transfection
• Transferrin (metabolism)
• Vesicle-Associated Membrane Protein 2 (genetics, metabolism)