Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
42
pubmed:dateCreated
2001-10-15
pubmed:abstractText
Rab11a is a small GTP-binding protein enriched in the pericentriolar plasma membrane recycling systems. We hypothesized that Rab11a-binding proteins exist as downstream effectors of its action. Here we define a family of four Rab11-interacting proteins: Rab11-Family Interacting Protein 1 (Rab11-FIP1), Rab11-Family Interacting Protein 2 (Rab11-FIP2), Rab11-Family Interacting Protein 3 (Rab11-FIP3), and pp75/Rip11. All four interacting proteins associated with wild type Rab11a and dominant active Rab11a (Rab11aS20V) as well as Rab11b and Rab25. Rab11-FIP2 also interacted with dominant negative Rab11a (Rab11aS25N) and the tail of myosin Vb. The binding of Rab11-FIP1, Rab11-FIP2, and Rab11-FIP3 to Rab11a was dependent upon a conserved carboxyl-terminal amphipathic alpha-helix. Rab11-FIP1, Rab11-FIP2, and pp75/Rip11 colocalized with Rab11a in plasma membrane recycling systems in both non-polarized HeLa cells and polarized Madin-Darby canine kidney cells. GFP-Rab11-FIP3 also colocalized with Rab11a in HeLa cells. Rab11-FIP1, Rab11-FIP2, and pp75/Rip11 also coenriched with Rab11a and H(+)K(+)-ATPase on parietal cell tubulovesicles, and Rab11-FIP1 and Rab11-FIP2 translocated with Rab11a and the H(+)K(+)-ATPase upon stimulating parietal cells with histamine. The results suggest that the function of Rab11a in plasma membrane recycling systems is dependent upon a compendium of protein effectors.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
19
pubmed:volume
276
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
39067-75
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:11495908-Amino Acid Sequence, pubmed-meshheading:11495908-Animals, pubmed-meshheading:11495908-Antineoplastic Agents, pubmed-meshheading:11495908-Antineoplastic Agents, Phytogenic, pubmed-meshheading:11495908-Base Sequence, pubmed-meshheading:11495908-Blotting, Western, pubmed-meshheading:11495908-Cell Line, pubmed-meshheading:11495908-Cell Membrane, pubmed-meshheading:11495908-Cloning, Molecular, pubmed-meshheading:11495908-Conserved Sequence, pubmed-meshheading:11495908-DNA, Complementary, pubmed-meshheading:11495908-Dogs, pubmed-meshheading:11495908-Expressed Sequence Tags, pubmed-meshheading:11495908-Gastric Mucosa, pubmed-meshheading:11495908-Gene Deletion, pubmed-meshheading:11495908-Gene Library, pubmed-meshheading:11495908-Genes, Dominant, pubmed-meshheading:11495908-HeLa Cells, pubmed-meshheading:11495908-Histamine, pubmed-meshheading:11495908-Humans, pubmed-meshheading:11495908-Microscopy, Fluorescence, pubmed-meshheading:11495908-Molecular Sequence Data, pubmed-meshheading:11495908-Nocodazole, pubmed-meshheading:11495908-Paclitaxel, pubmed-meshheading:11495908-Protein Binding, pubmed-meshheading:11495908-Rabbits, pubmed-meshheading:11495908-Recombinant Proteins, pubmed-meshheading:11495908-Sequence Homology, Amino Acid, pubmed-meshheading:11495908-Two-Hybrid System Techniques, pubmed-meshheading:11495908-rab GTP-Binding Proteins
pubmed:year
2001
pubmed:articleTitle
Identification and characterization of a family of Rab11-interacting proteins.
pubmed:affiliation
Department of Medicine, Institute of Molecular Medicine and Genetics, Medical College of Georgia and the Augusta Veterans Affairs Medical Center, Augusta, Georgia 30912, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.