Literature DB >> 9714795

Clathrin and adaptors.

J Hirst1, M S Robinson.   

Abstract

Clathrin and adaptors are components of clathrin-coated pits and vesicles. The AP-1 adaptor complex is associated with clathrin-coated vesicles budding from the TGN, while the AP-2 adaptor complex is associated with clathrin-coated vesicles budding from the plasma membrane. The clathrin forms a polyhedral lattice and is believed to be the driving force behind membrane invagination leading to vesicle budding. The adaptors attach the clathrin to the membrane and also interact with the cytoplasmic domains of selected transmembrane proteins, causing these proteins to become concentrated in clathrin-coated vesicles. Clathrin-coated vesicles budding from the TGN have been implicated in the sorting of newly synthesised lysosomal enzymes, while clathrin-coated vesicles budding from the plasma membrane facilitate the receptor-mediated endocytosis of ligands, such as low density lipoproteins and transferrin. A novel adaptor-related complex, AP-3, has recently been identified, which is recruited onto membranes of the TGN and a more peripheral compartment but does not appear to be associated with clathrin. Genetic studies indicate that AP-3 plays a role in the sorting of proteins to lysosomes and lysosome-related organelles.

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Year:  1998        PMID: 9714795     DOI: 10.1016/s0167-4889(98)00056-1

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  117 in total

1.  The assembly of AP-3 adaptor complex-containing clathrin-coated vesicles on synthetic liposomes.

Authors:  M T Drake; Y Zhu; S Kornfeld
Journal:  Mol Biol Cell       Date:  2000-11       Impact factor: 4.138

2.  The cytosolic C-terminus of the glucose transporter GLUT4 contains an acidic cluster endosomal targeting motif distal to the dileucine signal.

Authors:  A M Shewan; B J Marsh; D R Melvin; S Martin; G W Gould; D E James
Journal:  Biochem J       Date:  2000-08-15       Impact factor: 3.857

3.  COP I domains required for coatomer integrity, and novel interactions with ARF and ARF-GAP.

Authors:  A Eugster; G Frigerio; M Dale; R Duden
Journal:  EMBO J       Date:  2000-08-01       Impact factor: 11.598

4.  Hrs recruits clathrin to early endosomes.

Authors:  C Raiborg; K G Bache; A Mehlum; E Stang; H Stenmark
Journal:  EMBO J       Date:  2001-09-03       Impact factor: 11.598

5.  GGA proteins associate with Golgi membranes through interaction between their GGAH domains and ADP-ribosylation factors.

Authors:  Hiroyuki Takatsu; Kaori Yoshino; Kyoko Toda; Kazuhisa Nakayama
Journal:  Biochem J       Date:  2002-07-15       Impact factor: 3.857

6.  Role of adaptor complex AP-3 in targeting wild-type and mutated CD63 to lysosomes.

Authors:  Brian A Rous; Barbara J Reaves; Gudrun Ihrke; John A G Briggs; Sally R Gray; David J Stephens; George Banting; J Paul Luzio
Journal:  Mol Biol Cell       Date:  2002-03       Impact factor: 4.138

7.  Cytoplasmic domain of herpes simplex virus gE causes accumulation in the trans-Golgi network, a site of virus envelopment and sorting of virions to cell junctions.

Authors:  T N McMillan; D C Johnson
Journal:  J Virol       Date:  2001-02       Impact factor: 5.103

8.  The delta subunit of AP-3 is required for efficient transport of VSV-G from the trans-Golgi network to the cell surface.

Authors:  Noriyuki Nishimura; Helen Plutner; Klaus Hahn; William E Balch
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-07       Impact factor: 11.205

9.  The polarized epithelia-specific mu 1B-adaptin complements mu 1A-deficiency in fibroblasts.

Authors:  Eeva-Liisa Eskelinen; Christoph Meyer; Hiroshi Ohno; Kurt von Figura; Peter Schu
Journal:  EMBO Rep       Date:  2002-04-18       Impact factor: 8.807

10.  Distinct and redundant functions of mu1 medium chains of the AP-1 clathrin-associated protein complex in the nematode Caenorhabditis elegans.

Authors:  J Shim; P W Sternberg; J Lee
Journal:  Mol Biol Cell       Date:  2000-08       Impact factor: 4.138

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