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Biochemical and Computational Analysis Of LNX1 Interacting Proteins
PDZ (Post-synaptic density, 95 kDa, Discs large, Zona Occludens-1) domains are protein interaction domains that bind to the carboxy-terminal amino acids of binding partners, heterodimerize with other PDZ domains, and also bind phosphoinositides. PDZ domain containing proteins are frequently involved...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3210812/ https://www.ncbi.nlm.nih.gov/pubmed/22087225 http://dx.doi.org/10.1371/journal.pone.0026248 |
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author | Wolting, Cheryl D. Griffiths, Emily K. Sarao, Renu Prevost, Brittany C. Wybenga-Groot, Leanne E. McGlade, C. Jane |
author_facet | Wolting, Cheryl D. Griffiths, Emily K. Sarao, Renu Prevost, Brittany C. Wybenga-Groot, Leanne E. McGlade, C. Jane |
author_sort | Wolting, Cheryl D. |
collection | PubMed |
description | PDZ (Post-synaptic density, 95 kDa, Discs large, Zona Occludens-1) domains are protein interaction domains that bind to the carboxy-terminal amino acids of binding partners, heterodimerize with other PDZ domains, and also bind phosphoinositides. PDZ domain containing proteins are frequently involved in the assembly of multi-protein complexes and clustering of transmembrane proteins. LNX1 (Ligand of Numb, protein X 1) is a RING (Really Interesting New Gene) domain-containing E3 ubiquitin ligase that also includes four PDZ domains suggesting it functions as a scaffold for a multi-protein complex. Here we use a human protein array to identify direct LNX1 PDZ domain binding partners. Screening of 8,000 human proteins with isolated PDZ domains identified 53 potential LNX1 binding partners. We combined this set with LNX1 interacting proteins identified by other methods to assemble a list of 220 LNX1 interacting proteins. Bioinformatic analysis of this protein list was used to select interactions of interest for future studies. Using this approach we identify and confirm six novel LNX1 binding partners: KCNA4, PAK6, PLEKHG5, PKC-alpha1, TYK2 and PBK, and suggest that LNX1 functions as a signalling scaffold. |
format | Online Article Text |
id | pubmed-3210812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32108122011-11-15 Biochemical and Computational Analysis Of LNX1 Interacting Proteins Wolting, Cheryl D. Griffiths, Emily K. Sarao, Renu Prevost, Brittany C. Wybenga-Groot, Leanne E. McGlade, C. Jane PLoS One Research Article PDZ (Post-synaptic density, 95 kDa, Discs large, Zona Occludens-1) domains are protein interaction domains that bind to the carboxy-terminal amino acids of binding partners, heterodimerize with other PDZ domains, and also bind phosphoinositides. PDZ domain containing proteins are frequently involved in the assembly of multi-protein complexes and clustering of transmembrane proteins. LNX1 (Ligand of Numb, protein X 1) is a RING (Really Interesting New Gene) domain-containing E3 ubiquitin ligase that also includes four PDZ domains suggesting it functions as a scaffold for a multi-protein complex. Here we use a human protein array to identify direct LNX1 PDZ domain binding partners. Screening of 8,000 human proteins with isolated PDZ domains identified 53 potential LNX1 binding partners. We combined this set with LNX1 interacting proteins identified by other methods to assemble a list of 220 LNX1 interacting proteins. Bioinformatic analysis of this protein list was used to select interactions of interest for future studies. Using this approach we identify and confirm six novel LNX1 binding partners: KCNA4, PAK6, PLEKHG5, PKC-alpha1, TYK2 and PBK, and suggest that LNX1 functions as a signalling scaffold. Public Library of Science 2011-11-08 /pmc/articles/PMC3210812/ /pubmed/22087225 http://dx.doi.org/10.1371/journal.pone.0026248 Text en Wolting et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wolting, Cheryl D. Griffiths, Emily K. Sarao, Renu Prevost, Brittany C. Wybenga-Groot, Leanne E. McGlade, C. Jane Biochemical and Computational Analysis Of LNX1 Interacting Proteins |
title | Biochemical and Computational Analysis Of LNX1 Interacting Proteins |
title_full | Biochemical and Computational Analysis Of LNX1 Interacting Proteins |
title_fullStr | Biochemical and Computational Analysis Of LNX1 Interacting Proteins |
title_full_unstemmed | Biochemical and Computational Analysis Of LNX1 Interacting Proteins |
title_short | Biochemical and Computational Analysis Of LNX1 Interacting Proteins |
title_sort | biochemical and computational analysis of lnx1 interacting proteins |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3210812/ https://www.ncbi.nlm.nih.gov/pubmed/22087225 http://dx.doi.org/10.1371/journal.pone.0026248 |
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