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Hsp72 Is an Intracellular Target of the α,β-Unsaturated Sesquiterpene Lactone, Parthenolide

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The electrophilic natural product parthenolide has generated significant interest as a model for potential chemotherapeutics. Similar to other α,β-unsaturated carbonyl electrophiles, parthenolide induces the heat shock response in leukemia cells, potentially through covalent adduction of heat shock proteins. Other thiol-reactive electrophiles have also been shown to induce the heat shock response as well as to covalently adduct members of the heat shock protein family, such as heat shock protein 72 (Hsp72). To identify sites of modification of Hsp72 by parthenolide, we used high-resolution tandem mass spectrometry to detect 10 lysine, histidine, and cysteine residues of recombinant Hsp72 as modified in vitro by 10 and 100 μM parthenolide. To further ascertain that modification of Hsp72 by parthenolide occurs inside cells and not simply as an in vitro artifact, an alkyne-labeled derivative of parthenolide was synthesized to enable enrichment and detection of protein targets of parthenolide using copper-catalyzed [3 + 2] azide–alkyne cycloaddition. The alkyne-labeled parthenolide derivative displays an half maximal inhibitory concentration (IC50) in undifferentiated acute monocytic leukemia cells (THP-1) of 13.1 ± 1.1 μM, whereas parthenolide has an IC50 of 4.7 ± 1.1 μM. Concentration dependence of protein modification by the alkyne–parthenolide derivative was demonstrated, as well as in vitro adduction of Hsp72. Following treatment of THP-1 cells in culture by the alkyne–parthenolide, adducted proteins were isolated with neutravidin resin and detected by immunoblotting in the enriched protein fraction. Hsp70 proteins were detected in the enriched proteins, indicating that Hsp70 proteins were adducted intracellularly by the alkyne–parthenolide derivative.

Shin, Myungsun, Andrew McGowan, Gabriel J. DiNatale, Thanprakorn Chiramanewong, Tianyi Cai, and Rebecca E. Connor. Hsp72 Is an Intracellular Target of the α,β-Unsaturated Sesquiterpene Lactone, Parthenolide. ACS Omega 2, no. 10 (2017): 7267-7274. http://pubs.acs.org/doi/full/10.1021/acsomega.7b00954

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This is an Open Access article published under an ACS AuthorChoice License, which permits
copying and redistribution of the article or any adaptations for non-commercial purposes.

Open access publication of this article was made possible with grant support from Waidner-Spahr Library distributed through the Dickinson College Research & Development Committee.

Rebecca Connor is a professor of Chemistry at Dickinson College.
Thanprakorn Chiramanewong and Tianyi Cai, Dickinson College class of 2013.
Myungsun Shin and Gabriel J. DiNatale, Dickinson College class of 2014.
Andrew McGowan, Dickinson College class of 2016.

This published version is made available on Dickinson Scholar with the permission of the publisher. For more information on the published version, visit ACS Publication's Website. https://pubs.acs.org/doi/10.1021/acsomega.7b00954


MLA citation style (9th ed.)

Shin, Myungsun , et al. Hsp72 Is an Intracellular Target of the Α,β-unsaturated Sesquiterpene Lactone, Parthenolide. . 2017. dickinson.hykucommons.org/concern/generic_works/264e3b07-af83-477f-9a8b-47cb154d04dd?q=2022.

APA citation style (7th ed.)

S. Myungsun, M. Andrew, D. G. J., C. Thanprakorn, C. Tianyi, & C. R. E. (2017). Hsp72 Is an Intracellular Target of the α,β-Unsaturated Sesquiterpene Lactone, Parthenolide. https://dickinson.hykucommons.org/concern/generic_works/264e3b07-af83-477f-9a8b-47cb154d04dd?q=2022

Chicago citation style (CMOS 17, author-date)

Shin, Myungsun , McGowan, Andrew , DiNatale, Gabriel J. , Chiramanewong, Thanprakorn , Cai, Tianyi , and Connor, Rebecca E. . Hsp72 Is an Intracellular Target of the Α,β-Unsaturated Sesquiterpene Lactone, Parthenolide. 2017. https://dickinson.hykucommons.org/concern/generic_works/264e3b07-af83-477f-9a8b-47cb154d04dd?q=2022.

Note: These citations are programmatically generated and may be incomplete.