Identification of alkylation-sensitive target chaperone proteins and their reactivity with natural products containing Michael acceptor - PubMed (original) (raw)
Comparative Study
. 2003 Dec;26(12):1047-54.
doi: 10.1007/BF02994757.
Affiliations
- PMID: 14723339
- DOI: 10.1007/BF02994757
Comparative Study
Identification of alkylation-sensitive target chaperone proteins and their reactivity with natural products containing Michael acceptor
Xi-Wen Liu et al. Arch Pharm Res. 2003 Dec.
Abstract
Molecular chaperones have a crucial role in the folding of nascent polypeptides in endoplasmic reticulum. Some of them are known to be sensitive to the modification by electrophilic metabolites of organic pro-toxicants. In order to identify chaperone proteins sensitive to alkyators, ER extract was subjected to alkylation by 4-acetamido-4'-maleimidyl-stilbene-2,2'-disulfonate (AMS), and subsequent SDS-PAGE analyses. Protein spots, with molecular mass of 160, 100, 57 and 36 kDa, were found to be sensitive to AMS alkylation, and one abundant chaperon protein was identified to be protein disulfide isomerase (PDI) in comparison with the purified PDI. To see the reactivity of PDI with cysteine alkylators, the reduced form (PDIred) of PDI was incubated with various alkylators containing Michael acceptor structure for 30 min at 38 degrees C at pH 6.3, and the remaining activity was determined by the insulin reduction assay. Iodoacetamide or N-ethylmaleimide at 0.1 mM remarkably inactivated PDIred with N-ethylmaleimide being more potent than iodoacetamide. A partial inactivation of PDIoxid was expressed by iodoacetamide, but not N-ethylmaleimide (NEM) at pH 6.3. Of Michael acceptor compounds tested, 1,4-benzoquinone (IC50, 15 microM) was the most potent, followed by 4-hydroxy-2-nonenal and 1,4-naphthoquinone. In contrast, 1,2-naphthoquinone, devoid of a remarkable inactivation action, was effective to cause the oxidative conversion of PDIred to PDIoxid. Thus, the action of Michael acceptor compounds differed greatly depending on their structure. Based on these, it is proposed that PDI, one of chaperone proteins in ER, could be susceptible to endogenous or xenobiotic Michael acceptor compounds in vivo system.
Similar articles
- Ribostamycin inhibits the chaperone activity of protein disulfide isomerase.
Horibe T, Nagai H, Sakakibara K, Hagiwara Y, Kikuchi M. Horibe T, et al. Biochem Biophys Res Commun. 2001 Dec 21;289(5):967-72. doi: 10.1006/bbrc.2001.6105. Biochem Biophys Res Commun. 2001. PMID: 11741285 - Protein disulfide isomerase modification and inhibition contribute to ER stress and apoptosis induced by oxidized low density lipoproteins.
Muller C, Bandemer J, Vindis C, Camaré C, Mucher E, Guéraud F, Larroque-Cardoso P, Bernis C, Auge N, Salvayre R, Negre-Salvayre A. Muller C, et al. Antioxid Redox Signal. 2013 Mar 1;18(7):731-42. doi: 10.1089/ars.2012.4577. Epub 2012 Dec 21. Antioxid Redox Signal. 2013. PMID: 23083489 - Protein disulfide isomerase: the multifunctional redox chaperone of the endoplasmic reticulum.
Noiva R. Noiva R. Semin Cell Dev Biol. 1999 Oct;10(5):481-93. doi: 10.1006/scdb.1999.0319. Semin Cell Dev Biol. 1999. PMID: 10597631 Review.
Cited by
- Scaffold Hopping of α-Rubromycin Enables Direct Access to FDA-Approved Cromoglicic Acid as a SARS-CoV-2 MPro Inhibitor.
Alhadrami HA, Sayed AM, Al-Khatabi H, Alhakamy NA, Rateb ME. Alhadrami HA, et al. Pharmaceuticals (Basel). 2021 Jun 5;14(6):541. doi: 10.3390/ph14060541. Pharmaceuticals (Basel). 2021. PMID: 34198933 Free PMC article. - Formation and Biological Targets of Quinones: Cytotoxic versus Cytoprotective Effects.
Bolton JL, Dunlap T. Bolton JL, et al. Chem Res Toxicol. 2017 Jan 17;30(1):13-37. doi: 10.1021/acs.chemrestox.6b00256. Epub 2016 Sep 29. Chem Res Toxicol. 2017. PMID: 27617882 Free PMC article. - Melatonin supplementation enhances browning suppression and improves transformation efficiency and regeneration of transgenic rough lemon plants (Citrus × jambhiri).
Mahmoud LM, Killiny N, Dutt M. Mahmoud LM, et al. PLoS One. 2024 Mar 6;19(3):e0294318. doi: 10.1371/journal.pone.0294318. eCollection 2024. PLoS One. 2024. PMID: 38446779 Free PMC article. - Formation and biological targets of botanical o-quinones.
Bolton JL, Dunlap TL, Dietz BM. Bolton JL, et al. Food Chem Toxicol. 2018 Oct;120:700-707. doi: 10.1016/j.fct.2018.07.050. Epub 2018 Jul 29. Food Chem Toxicol. 2018. PMID: 30063944 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources