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
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
e13738Subventions
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.
Références
Elife. 2017 Jun 08;6:
pubmed: 28594326
Exp Mol Pathol. 2012 Feb;92(1):97-104
pubmed: 22101259
J Biotechnol. 2006 Dec 1;126(4):554-61
pubmed: 16797767
Science. 2006 Aug 25;313(5790):1137-40
pubmed: 16931765
Diabetes Obes Metab. 2009 Sep;11(9):823-35
pubmed: 19531057
J Clin Invest. 1997 Nov 15;100(10):2457-65
pubmed: 9366560
BMC Bioinformatics. 2021 Sep 10;22(1):433
pubmed: 34507520
Anticancer Res. 1999 May-Jun;19(3A):1971-6
pubmed: 10470142
Aging Cell. 2022 Dec;21(12):e13738
pubmed: 36373957
FEMS Yeast Res. 2018 Mar 1;18(2):
pubmed: 29452364
Nat Methods. 2009 Apr;6(4):275-7
pubmed: 19305406
Toxicol Lett. 2017 Apr 5;271:26-37
pubmed: 28245985
Cell. 2013 Jun 6;153(6):1194-217
pubmed: 23746838
Nature. 1999 Jan 21;397(6716):271-4
pubmed: 9930704
Proc Natl Acad Sci U S A. 2000 Feb 15;97(4):1796-801
pubmed: 10677536
J Pediatr. 2001 Jan;138(1 Suppl):S46-54; discussion S54-5
pubmed: 11148549
Chem Biol Interact. 2015 Dec 5;242:99-106
pubmed: 26428355