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Publication : The phosphatidylinositol transfer protein RdgB? binds 14-3-3 via its unstructured C-terminus, whereas its lipid-binding domain interacts with the integral membrane protein ATRAP (angiotensin II type?I receptor-associated protein).

First Author  Garner K Year  2011
Journal  Biochem J Volume  439
Issue  1 Pages  97-111
PubMed ID  21728994 Mgi Jnum  J:389220
Mgi Id  MGI:8386182 Doi  10.1042/BJ20110649
Citation  Garner K, et al. (2011) The phosphatidylinositol transfer protein RdgBbeta binds 14-3-3 via its unstructured C-terminus, whereas its lipid-binding domain interacts with the integral membrane protein ATRAP (angiotensin II type I receptor-associated protein). Biochem J 439(1):97-111
abstractText  PITPs [PI (phosphatidylinositol) transfer proteins] bind and transfer PI between intracellular membranes and participate in many cellular processes including signalling, lipid metabolism and membrane traffic. The largely uncharacterized PITP RdgBbeta (PITPNC1; retinal degeneration type B beta), contains a long C-terminal disordered region following its defining N-terminal PITP domain. In the present study we report that the C-terminus contains two tandem phosphorylated binding sites (Ser(274) and Ser(299)) for 14-3-3. The C-terminus also contains PEST sequences which are shielded by 14-3-3 binding. Like many proteins containing PEST sequences, the levels of RdgBbeta are regulated by proteolysis. RdgBbeta is degraded with a half-life of 4 h following ubiquitination via the proteasome. A mutant RdgBbeta which is unable to bind 14-3-3 is degraded even faster with a half-life of 2 h. In vitro, RdgBbeta is 100-fold less active than PITPalpha for PI transfer, and RdgBbeta proteins (wild-type and a mutant that cannot bind 14-3-3) expressed in COS-7 cells or endogenous proteins from heart cytosol do not exhibit transfer activity. When cells are treated with PMA, the PITP domain of RdgBbeta interacts with the integral membrane protein ATRAP (angiotensin II type I receptor-associated protein; also known as AGTRAP) causing membrane recruitment. We suggest that RdgBbeta executes its function following recruitment to membranes via its PITP domain and the C-terminal end of the protein could regulate entry to the hydrophobic cavity.
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