4-phenylbutyric acid-Identity crisis; can it act as a translation inhibitor?

4PBA Proteostasis chemical chaperone protein synthesis translation inhibition unfolded protein response

Journal

Aging cell
ISSN: 1474-9726
Titre abrégé: Aging Cell
Pays: England
ID NLM: 101130839

Informations de publication

Date de publication:
Dec 2022
Historique:
revised: 30 09 2022
received: 14 06 2022
accepted: 21 10 2022
pubmed: 15 11 2022
medline: 15 12 2022
entrez: 14 11 2022
Statut: ppublish

Résumé

Loss of proteostasis can occur due to mutations, the formation of aggregates, or general deficiency in the correct translation and folding of proteins. These phenomena are commonly observed in pathologies, but most significantly, loss of proteostasis characterizes aging. This loss leads to the chronic activation of stress responses and has a generally deleterious impact on the organism. While finding molecules that can alleviate these symptoms is an important step toward solutions for these conditions, some molecules might be mischaracterized on the way. 4-phenylbutyric acid (4PBA) is known for its role as a chemical chaperone that helps alleviate endoplasmic reticulum (ER) stress, yet a scan of the literature reveals that no biochemical or molecular experiments have shown any protein refolding capacity. Here, we show that 4PBA is a conserved weak inhibitor of mRNA translation, both in vitro and in cellular systems, and furthermore-it does not promote protein folding nor prevents aggregation. 4PBA possibly alleviates proteostatic or ER stress by inhibiting protein synthesis, allowing the cells to cope with misfolded proteins by reducing the protein load. Better understanding of 4PBA biochemical mechanisms will improve its usage in basic science and as a drug in different pathologies, also opening new venues for the treatment of different diseases.

Identifiants

pubmed: 36373957
doi: 10.1111/acel.13738
pmc: PMC9741500
doi:

Substances chimiques

4-phenylbutyric acid 7WY7YBI87E
Phenylbutyrates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13738

Subventions

Organisme : David and Inez Myers Foundation
Organisme : Bio-tech and Negev fellowships of Kreitman School of Advanced Research of Ben Gurion University

Informations de copyright

© 2022 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd.

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Auteurs

Daniel Stein (D)

Department of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
The Zlotowski Center for Neuroscience, Ben-Gurion University of the Negev, Beer Sheva, Israel.

Zeev Slobodnik (Z)

Department of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
The Zlotowski Center for Neuroscience, Ben-Gurion University of the Negev, Beer Sheva, Israel.

Benjamin Tam (B)

Department of Chemistry, Ben-Gurion University of the Negev, Beer Sheva, Israel.

Monica Einav (M)

Department of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
The Zlotowski Center for Neuroscience, Ben-Gurion University of the Negev, Beer Sheva, Israel.

Barak Akabayov (B)

Department of Chemistry, Ben-Gurion University of the Negev, Beer Sheva, Israel.

Shimon Berstein (S)

Department of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.

Debra Toiber (D)

Department of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva, Israel.
The Zlotowski Center for Neuroscience, Ben-Gurion University of the Negev, Beer Sheva, Israel.

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Classifications MeSH