Zinc-chelating postsynaptic density-95 N-terminus impairs its palmitoyl modification.


Journal

Protein science : a publication of the Protein Society
ISSN: 1469-896X
Titre abrégé: Protein Sci
Pays: United States
ID NLM: 9211750

Informations de publication

Date de publication:
11 2021
Historique:
revised: 10 09 2021
received: 07 07 2021
accepted: 17 09 2021
pubmed: 20 9 2021
medline: 25 12 2021
entrez: 19 9 2021
Statut: ppublish

Résumé

Chemical synaptic transmission represents the most sophisticated dynamic process and is highly regulated with optimized neurotransmitter balance. Imbalanced transmitters can lead to transmission impairments, for example, intracellular zinc accumulation is a hallmark of degenerating neurons. However, the underlying mechanisms remain elusive. Postsynaptic density protein-95 (PSD-95) is a primary postsynaptic membrane-associated protein and the major scaffolding component in the excitatory postsynaptic densities, which performs substantial functions in synaptic development and maturation. Its membrane association induced by palmitoylation contributes largely to its regulatory functions at postsynaptic sites. Unlike other structural domains in PSD-95, the N-terminal region (PSD-95NT) is flexible and interacts with various targets, which modulates its palmitoylation of two cysteines (C3/C5) and glutamate receptor distributions in postsynaptic densities. PSD-95NT contains a putative zinc-binding motif (C2H2) with undiscovered functions. This study is the first effort to investigate the interaction between Zn

Identifiants

pubmed: 34538002
doi: 10.1002/pro.4187
pmc: PMC8521293
doi:

Substances chimiques

Chelating Agents 0
DLG4 protein, human 0
Disks Large Homolog 4 Protein 0
Zinc J41CSQ7QDS

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2246-2257

Informations de copyright

© 2021 The Protein Society.

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Auteurs

Yonghong Zhang (Y)

Department of Chemistry, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Xiaoqian Fang (X)

Department of Molecular Science, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Luis Ascota (L)

Department of Chemistry, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.
Department of Molecular Science, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Libo Li (L)

Department of Chemistry, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.
Key Laboratory of Green Chemical Engineering and Technology of College of Heilongjiang Province, College of Chemical and Environmental Engineering, Harbin University of Science and Technology, Harbin, China.

Lili Guerra (L)

Department of Molecular Science, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Audrey Vega (A)

Department of Chemistry, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Amanda Salinas (A)

Department of Chemistry, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Andrea Gonzalez (A)

Department of Chemistry, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Claudia Garza (C)

Department of Chemistry, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Andrew Tsin (A)

Department of Molecular Science, The University of Texas Rio Grande Valley, Edinburg, Texas, USA.

Johannes W Hell (JW)

Department of Pharmacology, University of California, Davis, California, USA.

James B Ames (JB)

Department of Chemistry, University of California, Davis, California, USA.

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Classifications MeSH