Cargando…

Comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope

The nuclear envelope (NE) is a subdomain of the ER with prominent roles in nuclear organization, largely mediated by its distinctive protein composition. We developed methods to reveal novel, low abundance transmembrane (TM) proteins concentrated at the NE relative to the peripheral ER. Using label-...

Descripción completa

Detalles Bibliográficos
Autores principales: Cheng, Li-Chun, Zhang, Xi, Baboo, Sabyasachi, Nguyen, Julie A, Martinez-Bartolomé, Salvador, Loose, Esther, Diedrich, Jolene, Yates, John R, Gerace, Larry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949040/
https://www.ncbi.nlm.nih.gov/pubmed/36824861
http://dx.doi.org/10.1101/2023.02.13.528342
_version_ 1784892898393718784
author Cheng, Li-Chun
Zhang, Xi
Baboo, Sabyasachi
Nguyen, Julie A
Martinez-Bartolomé, Salvador
Loose, Esther
Diedrich, Jolene
Yates, John R
Gerace, Larry
author_facet Cheng, Li-Chun
Zhang, Xi
Baboo, Sabyasachi
Nguyen, Julie A
Martinez-Bartolomé, Salvador
Loose, Esther
Diedrich, Jolene
Yates, John R
Gerace, Larry
author_sort Cheng, Li-Chun
collection PubMed
description The nuclear envelope (NE) is a subdomain of the ER with prominent roles in nuclear organization, largely mediated by its distinctive protein composition. We developed methods to reveal novel, low abundance transmembrane (TM) proteins concentrated at the NE relative to the peripheral ER. Using label-free proteomics that compared isolated NEs to cytoplasmic membranes, we first identified proteins with apparent NE enrichment. In subsequent authentication, ectopically expressed candidates were analyzed by immunofluorescence microscopy to quantify their targeting to the NE in cultured cells. Ten proteins from a validation set were found to associate preferentially with the NE, including oxidoreductases, enzymes for lipid biosynthesis and regulators of cell growth and survival. We determined that one of the validated candidates, the palmitoyltransferase Zdhhc6, modifies the NE oxidoreductase Tmx4 and thereby modulates its NE levels. This provides a functional rationale for the NE concentration of Zdhhc6. Overall, our methodology has revealed a group of previously unrecognized proteins concentrated at the NE and additional candidates. Future analysis of these can potentially unveil new mechanistic pathways associated with the NE.
format Online
Article
Text
id pubmed-9949040
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-99490402023-02-24 Comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope Cheng, Li-Chun Zhang, Xi Baboo, Sabyasachi Nguyen, Julie A Martinez-Bartolomé, Salvador Loose, Esther Diedrich, Jolene Yates, John R Gerace, Larry bioRxiv Article The nuclear envelope (NE) is a subdomain of the ER with prominent roles in nuclear organization, largely mediated by its distinctive protein composition. We developed methods to reveal novel, low abundance transmembrane (TM) proteins concentrated at the NE relative to the peripheral ER. Using label-free proteomics that compared isolated NEs to cytoplasmic membranes, we first identified proteins with apparent NE enrichment. In subsequent authentication, ectopically expressed candidates were analyzed by immunofluorescence microscopy to quantify their targeting to the NE in cultured cells. Ten proteins from a validation set were found to associate preferentially with the NE, including oxidoreductases, enzymes for lipid biosynthesis and regulators of cell growth and survival. We determined that one of the validated candidates, the palmitoyltransferase Zdhhc6, modifies the NE oxidoreductase Tmx4 and thereby modulates its NE levels. This provides a functional rationale for the NE concentration of Zdhhc6. Overall, our methodology has revealed a group of previously unrecognized proteins concentrated at the NE and additional candidates. Future analysis of these can potentially unveil new mechanistic pathways associated with the NE. Cold Spring Harbor Laboratory 2023-02-14 /pmc/articles/PMC9949040/ /pubmed/36824861 http://dx.doi.org/10.1101/2023.02.13.528342 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Cheng, Li-Chun
Zhang, Xi
Baboo, Sabyasachi
Nguyen, Julie A
Martinez-Bartolomé, Salvador
Loose, Esther
Diedrich, Jolene
Yates, John R
Gerace, Larry
Comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope
title Comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope
title_full Comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope
title_fullStr Comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope
title_full_unstemmed Comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope
title_short Comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope
title_sort comparative membrane proteomics reveals diverse cell regulators concentrated at the nuclear envelope
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949040/
https://www.ncbi.nlm.nih.gov/pubmed/36824861
http://dx.doi.org/10.1101/2023.02.13.528342
work_keys_str_mv AT chenglichun comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope
AT zhangxi comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope
AT baboosabyasachi comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope
AT nguyenjuliea comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope
AT martinezbartolomesalvador comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope
AT looseesther comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope
AT diedrichjolene comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope
AT yatesjohnr comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope
AT geracelarry comparativemembraneproteomicsrevealsdiversecellregulatorsconcentratedatthenuclearenvelope