Johannes Reynisson j.reynisson@keele.ac.uk
Identification of Isoform-Selective Ligands for the Middle Domain of Heat Shock Protein 90 (Hsp90)
Reynisson
Authors
Abstract
The molecular chaperone heat shock protein 90 (Hsp90) is a current inhibition target for the treatment of diseases, including cancer. In humans, there are two major cytosolic isoforms of Hsp90 (Hsp90a and Hsp90ß). Hsp90a is inducible and Hsp90ß is constitutively expressed. Most Hsp90 inhibitors are pan-inhibitors that target both cytosolic isoforms of Hsp90. The development of isoform-selective inhibitors of Hsp90 may enable better clinical outcomes. Herein, by using virtual screening and binding studies, we report our work in the identification and characterisation of novel isoform-selective ligands for the middle domain of Hsp90ß. Our results pave the way for further development of isoform-selective Hsp90 inhibitors.
Citation
Reynisson. (2019). Identification of Isoform-Selective Ligands for the Middle Domain of Heat Shock Protein 90 (Hsp90). International Journal of Molecular Sciences, https://doi.org/10.3390/ijms20215333
Acceptance Date | Oct 23, 2019 |
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Publication Date | Oct 26, 2019 |
Journal | International Journal of Molecular Sciences |
Print ISSN | 1661-6596 |
Publisher | MDPI |
DOI | https://doi.org/10.3390/ijms20215333 |
Keywords | Hsp90, intrinsic tryptophan fluorescence, isoform-selective, ligand binding, virtual screening |
Publisher URL | http://doi.org/10.3390/ijms20215333 |
Files
ijms-20-05333.pdf
(1.4 Mb)
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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