Cargando…
A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex
Endocytosis of transmembrane proteins is orchestrated by the AP2 clathrin adaptor complex. AP2 dwells in a closed, inactive state in the cytosol, but adopts an open, active conformation on the plasma membrane. Membrane-activated complexes are also phosphorylated, but the significance of this mark is...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739873/ https://www.ncbi.nlm.nih.gov/pubmed/31464684 http://dx.doi.org/10.7554/eLife.50003 |
_version_ | 1783451006336499712 |
---|---|
author | Partlow, Edward A Baker, Richard W Beacham, Gwendolyn M Chappie, Joshua S Leschziner, Andres E Hollopeter, Gunther |
author_facet | Partlow, Edward A Baker, Richard W Beacham, Gwendolyn M Chappie, Joshua S Leschziner, Andres E Hollopeter, Gunther |
author_sort | Partlow, Edward A |
collection | PubMed |
description | Endocytosis of transmembrane proteins is orchestrated by the AP2 clathrin adaptor complex. AP2 dwells in a closed, inactive state in the cytosol, but adopts an open, active conformation on the plasma membrane. Membrane-activated complexes are also phosphorylated, but the significance of this mark is debated. We recently proposed that NECAP negatively regulates AP2 by binding open and phosphorylated complexes (Beacham et al., 2018). Here, we report high-resolution cryo-EM structures of NECAP bound to phosphorylated AP2. The site of AP2 phosphorylation is directly coordinated by residues of the NECAP PHear domain that are predicted from genetic screens in C. elegans. Using membrane mimetics to generate conformationally open AP2, we find that a second domain of NECAP binds these complexes and cryo-EM reveals both domains of NECAP engaging closed, inactive AP2. Assays in vitro and in vivo confirm these domains cooperate to inactivate AP2. We propose that phosphorylation marks adaptors for inactivation. |
format | Online Article Text |
id | pubmed-6739873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-67398732019-09-13 A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex Partlow, Edward A Baker, Richard W Beacham, Gwendolyn M Chappie, Joshua S Leschziner, Andres E Hollopeter, Gunther eLife Cell Biology Endocytosis of transmembrane proteins is orchestrated by the AP2 clathrin adaptor complex. AP2 dwells in a closed, inactive state in the cytosol, but adopts an open, active conformation on the plasma membrane. Membrane-activated complexes are also phosphorylated, but the significance of this mark is debated. We recently proposed that NECAP negatively regulates AP2 by binding open and phosphorylated complexes (Beacham et al., 2018). Here, we report high-resolution cryo-EM structures of NECAP bound to phosphorylated AP2. The site of AP2 phosphorylation is directly coordinated by residues of the NECAP PHear domain that are predicted from genetic screens in C. elegans. Using membrane mimetics to generate conformationally open AP2, we find that a second domain of NECAP binds these complexes and cryo-EM reveals both domains of NECAP engaging closed, inactive AP2. Assays in vitro and in vivo confirm these domains cooperate to inactivate AP2. We propose that phosphorylation marks adaptors for inactivation. eLife Sciences Publications, Ltd 2019-08-29 /pmc/articles/PMC6739873/ /pubmed/31464684 http://dx.doi.org/10.7554/eLife.50003 Text en © 2019, Partlow et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Partlow, Edward A Baker, Richard W Beacham, Gwendolyn M Chappie, Joshua S Leschziner, Andres E Hollopeter, Gunther A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex |
title | A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex |
title_full | A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex |
title_fullStr | A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex |
title_full_unstemmed | A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex |
title_short | A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex |
title_sort | structural mechanism for phosphorylation-dependent inactivation of the ap2 complex |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739873/ https://www.ncbi.nlm.nih.gov/pubmed/31464684 http://dx.doi.org/10.7554/eLife.50003 |
work_keys_str_mv | AT partlowedwarda astructuralmechanismforphosphorylationdependentinactivationoftheap2complex AT bakerrichardw astructuralmechanismforphosphorylationdependentinactivationoftheap2complex AT beachamgwendolynm astructuralmechanismforphosphorylationdependentinactivationoftheap2complex AT chappiejoshuas astructuralmechanismforphosphorylationdependentinactivationoftheap2complex AT leschzinerandrese astructuralmechanismforphosphorylationdependentinactivationoftheap2complex AT hollopetergunther astructuralmechanismforphosphorylationdependentinactivationoftheap2complex AT partlowedwarda structuralmechanismforphosphorylationdependentinactivationoftheap2complex AT bakerrichardw structuralmechanismforphosphorylationdependentinactivationoftheap2complex AT beachamgwendolynm structuralmechanismforphosphorylationdependentinactivationoftheap2complex AT chappiejoshuas structuralmechanismforphosphorylationdependentinactivationoftheap2complex AT leschzinerandrese structuralmechanismforphosphorylationdependentinactivationoftheap2complex AT hollopetergunther structuralmechanismforphosphorylationdependentinactivationoftheap2complex |