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Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation

Palmitoylation regulates diverse aspects of neuronal protein trafficking and function. Here, a global characterization of the neuronal palmitoyl-proteome identifies most of the known neuronal palmitoyl-proteins (PPs), 68 in total, plus over 200 new PP candidates, with additional testing confirming p...

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Autores principales: Kang, Rujun, Wan, Junmei, Arstikaitis, Pamela, Takahashi, Hideto, Huang, Kun, Bailey, Aaron O., Thompson, James X., Roth, Amy F., Drisdel, Renaldo C., Mastro, Ryan, Green, William N., Yates, John R., Davis, Nicholas G., El-Husseini, Alaa
Formato: Texto
Lenguaje:English
Publicado: 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2610860/
https://www.ncbi.nlm.nih.gov/pubmed/19092927
http://dx.doi.org/10.1038/nature07605
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author Kang, Rujun
Wan, Junmei
Arstikaitis, Pamela
Takahashi, Hideto
Huang, Kun
Bailey, Aaron O.
Thompson, James X.
Roth, Amy F.
Drisdel, Renaldo C.
Mastro, Ryan
Green, William N.
Yates, John R.
Davis, Nicholas G.
El-Husseini, Alaa
author_facet Kang, Rujun
Wan, Junmei
Arstikaitis, Pamela
Takahashi, Hideto
Huang, Kun
Bailey, Aaron O.
Thompson, James X.
Roth, Amy F.
Drisdel, Renaldo C.
Mastro, Ryan
Green, William N.
Yates, John R.
Davis, Nicholas G.
El-Husseini, Alaa
author_sort Kang, Rujun
collection PubMed
description Palmitoylation regulates diverse aspects of neuronal protein trafficking and function. Here, a global characterization of the neuronal palmitoyl-proteome identifies most of the known neuronal palmitoyl-proteins (PPs), 68 in total, plus over 200 new PP candidates, with additional testing confirming palmitoylation for 21 of these candidates. New PPs include neurotransmitter receptors, transporters, adhesion molecules, scaffolding proteins, as well as SNAREs and other vesicular trafficking proteins. Of particular interest is a finding of palmitoylation for a brain-specific Cdc42 splice variant. The palmitoylated Cdc42 isoform (Cdc42-palm) differs from the canonical, prenylated form (Cdc42-prenyl) both with regard to localization and function: Cdc42-palm, concentrates in dendritic spines and plays a special role in inducing these post-synaptic structures. Finally, assessing palmitoylation dynamics in drug-induced activity paradigms finds rapidly induced changes both for Cdc42 as well as for other synaptic PPs, suggesting that palmitoylation may participate broadly in the activity-driven changes that shape synapse morphology and function.
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spelling pubmed-26108602009-06-18 Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation Kang, Rujun Wan, Junmei Arstikaitis, Pamela Takahashi, Hideto Huang, Kun Bailey, Aaron O. Thompson, James X. Roth, Amy F. Drisdel, Renaldo C. Mastro, Ryan Green, William N. Yates, John R. Davis, Nicholas G. El-Husseini, Alaa Nature Article Palmitoylation regulates diverse aspects of neuronal protein trafficking and function. Here, a global characterization of the neuronal palmitoyl-proteome identifies most of the known neuronal palmitoyl-proteins (PPs), 68 in total, plus over 200 new PP candidates, with additional testing confirming palmitoylation for 21 of these candidates. New PPs include neurotransmitter receptors, transporters, adhesion molecules, scaffolding proteins, as well as SNAREs and other vesicular trafficking proteins. Of particular interest is a finding of palmitoylation for a brain-specific Cdc42 splice variant. The palmitoylated Cdc42 isoform (Cdc42-palm) differs from the canonical, prenylated form (Cdc42-prenyl) both with regard to localization and function: Cdc42-palm, concentrates in dendritic spines and plays a special role in inducing these post-synaptic structures. Finally, assessing palmitoylation dynamics in drug-induced activity paradigms finds rapidly induced changes both for Cdc42 as well as for other synaptic PPs, suggesting that palmitoylation may participate broadly in the activity-driven changes that shape synapse morphology and function. 2008-12-18 /pmc/articles/PMC2610860/ /pubmed/19092927 http://dx.doi.org/10.1038/nature07605 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kang, Rujun
Wan, Junmei
Arstikaitis, Pamela
Takahashi, Hideto
Huang, Kun
Bailey, Aaron O.
Thompson, James X.
Roth, Amy F.
Drisdel, Renaldo C.
Mastro, Ryan
Green, William N.
Yates, John R.
Davis, Nicholas G.
El-Husseini, Alaa
Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation
title Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation
title_full Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation
title_fullStr Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation
title_full_unstemmed Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation
title_short Neural Palmitoyl-Proteomics Reveals Dynamic Synaptic Palmitoylation
title_sort neural palmitoyl-proteomics reveals dynamic synaptic palmitoylation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2610860/
https://www.ncbi.nlm.nih.gov/pubmed/19092927
http://dx.doi.org/10.1038/nature07605
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