APPL1 is a multifunctional endosomal signaling adaptor protein

被引:39
|
作者
Diggins, Nicole L. [1 ]
Webb, Donna J. [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Dept Biol Sci, 221 Kirkland Hall, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Vanderbilt Kennedy Ctr Res Human Dev, 221 Kirkland Hall, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Dept Canc Biol, 221 Kirkland Hall, Nashville, TN 37235 USA
基金
美国国家卫生研究院;
关键词
CELL-MIGRATION; PH DOMAIN; RECEPTOR; RAB5; AKT; TRAFFICKING; INTERACTS; FAMILY; ADHESION; PATHWAY;
D O I
10.1042/BST20160191
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
Endosomal adaptor proteins are important regulators of signaling pathways underlying many biological processes. These adaptors can integrate signals from multiple pathways via localization to specific endosomal compartments, as well as through multiple protein-protein interactions. One such adaptor protein that has been implicated in regulating signaling pathways is the adaptor protein containing a pleckstrin homology (PH) domain, phosphotyrosine-binding (PTB) domain, and leucine zipper motif 1 (APPL1). APPL1 localizes to a subset of Rab5-positive endosomes through its Bin-Amphiphysin-Rvs and PH domains, and it coordinates signaling pathways through its interaction with many signaling receptors and proteins through its PTB domain. This review discusses our current understanding of the role of APPL1 in signaling and trafficking, as well as highlights recent work into the function of APPL1 in cell migration and adhesion.
引用
收藏
页码:771 / 779
页数:9
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