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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...

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Autores principales: Wolting, Cheryl D., Griffiths, Emily K., Sarao, Renu, Prevost, Brittany C., Wybenga-Groot, Leanne E., McGlade, C. Jane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
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.
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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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