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Chembiochem. 2010 Mar 1;11(4):456-67. doi: 10.1002/cbic.200900616.

Structural diversity of PDZ-lipid interactions.

Author information

1
Department of Human Genetics, K.U.Leuven, Herestraat, 49 Box 602, 3000 Leuven, Belgium.

Abstract

PDZ domains are globular protein modules that are over-and-above appreciated for their interaction with short peptide motifs found in the cytosolic tail of membrane receptors, channels, and adhesion molecules. These domains predominate in scaffold molecules that control the assembly and the location of large signaling complexes. Studies have now emerged showing that PDZ domains can also interact with membrane lipids, and in particular with phosphoinositides. Phosphoinositides control various aspects of cell signaling, vesicular trafficking, and cytoskeleton remodeling. When investigated, lipid binding appears to be extremely relevant for PDZ protein functionality. Studies point to more than one mechanism for PDZ domains to associate with lipids. Few studies have been focused on the structural basis of PDZ-phosphoinositide interactions, and the biological consequences of such interactions. Using the current knowledge on syntenin-1, syntenin-2, PTP-Bas, PAR-3 and PICK1, we recapitulate our understanding of the structural and biochemical aspects of PDZ-lipid interactions and the consequences for peptide interactions.

PMID:
20091728
DOI:
10.1002/cbic.200900616
[Indexed for MEDLINE]

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