Definition of the consensus motif recognized by γ-adaptin ear domains

被引:54
作者
Mattera, R
Ritter, B
Sidhu, SS
McPherson, PS
Bonifacino, JS
机构
[1] NICHD, Cell Biol & Metab Branch, NIH, Bethesda, MD 20892 USA
[2] McGill Univ, Montreal Neurol Inst, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[3] Genentech Inc, Dept Prot Engn, San Francisco, CA 94080 USA
关键词
D O I
10.1074/jbc.M311873200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The heterotetrameric adaptor complex 1 (AP-1) and the monomeric Golgi-localized, gamma ear-containing, Arf-binding (GGA) proteins are components of clathrin coats associated with the trans-Golgi network and endosomes. The carboxyl-terminal ear domains (or gamma-adaptin ear (GAE) domains) of two gamma-adaptin subunit isoforms of AP-1 and of the GGAs are structurally similar and bind to a common set of accessory proteins. In this study, we have systematically defined a core tetrapeptide motif PsiG(P/D/E)(Psi/L/M) (where Psi is an aromatic residue), which is responsible for the interactions of accessory proteins with GAE domains. The definition of this motif has allowed us to identify novel GAE-binding partners named NECAP and aftiphilin, which also contain clathrin-binding motifs. These findings shed light on the mechanism of accessory protein recruitment to trans-Golgi network and endosomal clathrin coats.
引用
收藏
页码:8018 / 8028
页数:11
相关论文
共 36 条
[1]   Signal-binding specificity of the μ4 subunit of the adaptor protein complex AP-4 [J].
Aguilar, RC ;
Boehm, M ;
Gorshkova, I ;
Crouch, RJ ;
Tomita, K ;
Saito, T ;
Ohno, H ;
Bonifacino, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (16) :13145-13152
[2]   The ear of alpha-adaptin interacts with the COOH-terminal domain of the Eps15 protein [J].
Benmerah, A ;
Begue, B ;
DautryVarsat, A ;
CerfBensussan, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (20) :12111-12116
[3]   Accessory protein recruitment motifs in clathrin-mediated endocytosis [J].
Brett, TJ ;
Traub, LM ;
Fremont, DH .
STRUCTURE, 2002, 10 (06) :797-809
[4]   Biological basket weaving: Formation and function of clathrin-coated vesicles [J].
Brodsky, FM ;
Chen, CY ;
Knuehl, C ;
Towler, MC ;
Wakeham, DE .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2001, 17 :517-568
[5]   Structural basis for binding of accessory proteins by the appendage domain of GGAs [J].
Collins, BM ;
Praefcke, GJK ;
Robinson, MS ;
Owen, DJ .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (08) :607-613
[6]   Association of the AP-3 adaptor complex with clathrin [J].
Dell'Angelica, EC ;
Klumperman, J ;
Stoorvogel, W ;
Bonifacino, JS .
SCIENCE, 1998, 280 (5362) :431-434
[7]   Rapid identification of small binding motifs with high-throughput phage display: Discovery of peptidic antagonists of IGF-1 function [J].
Deshayes, K ;
Schaffer, ML ;
Skelton, NJ ;
Nakamura, GR ;
Kadkhodayan, S ;
Sidhu, SS .
CHEMISTRY & BIOLOGY, 2002, 9 (04) :495-505
[8]   ENTH/ANTH domains expand to the Golgi [J].
Duncan, MC ;
Payne, GS .
TRENDS IN CELL BIOLOGY, 2003, 13 (05) :211-215
[9]   Yeast epsin-related proteins required for Golgi-endosome traffic define a γ-adaptin ear-binding motif [J].
Duncan, MC ;
Costaguta, G ;
Payne, GS .
NATURE CELL BIOLOGY, 2003, 5 (01) :77-81
[10]   A family of proteins with γ-adaptin and VHS domains that facilitate trafficking between the trans-Golgi network and the vacuole/lysosome [J].
Hirst, J ;
Lui, WWY ;
Bright, NA ;
Totty, N ;
Seaman, MNJ ;
Robinson, MS .
JOURNAL OF CELL BIOLOGY, 2000, 149 (01) :67-79