Skip to main content

Research Repository

Advanced Search

The Small Molecule Antagonist KCI807 Disrupts Association of the Amino-Terminal Domain of the Androgen Receptor with ELK1 by Modulating the Adjacent DNA Binding Domain

Soave, Claire; Ducker, Charles; Islam, Naeyma; Kim, Seongho; Yurgelevic, Sally; Nicely, Nathan I.; Pardy, Luke; Huang, Yanfang; Shaw, Peter E.; Auner, Gregory; Dickson, Alex; Ratnam, Manohar

The Small Molecule Antagonist KCI807 Disrupts Association of the Amino-Terminal Domain of the Androgen Receptor with ELK1 by Modulating the Adjacent DNA Binding Domain Thumbnail


Authors

Claire Soave

Naeyma Islam

Seongho Kim

Sally Yurgelevic

Nathan I. Nicely

Luke Pardy

Yanfang Huang

Peter E. Shaw

Gregory Auner

Alex Dickson

Manohar Ratnam



Abstract

The androgen receptor (AR) is a crucial coactivator of ELK1 for prostate cancer (PCa) growth, associating with ELK1 through two peptide segments (358-457 and 514-557) within the amino-terminal domain (NTD) of AR. The small-molecule antagonist 5-hydroxy-2-(3-hydroxyphenyl)chromen-4-one (KCI807) binds to AR, blocking ELK1 binding and inhibiting PCa growth. We investigated the mode of interaction of KCI807 with AR using systematic mutagenesis coupled with ELK1 coactivation assays, testing polypeptide binding and Raman spectroscopy. In full-length AR, deletion of neither ELK1 binding segment affected sensitivity of residual ELK1 coactivation to KCI807. Although the NTD is sufficient for association of AR with ELK1, interaction of the isolated NTD with ELK1 was insensitive to KCI807. In contrast, coactivation of ELK1 by the AR-V7 splice variant, comprising the NTD and the DNA binding domain (DBD), was sensitive to KCI807. Deletions and point mutations within DBD segment 558-595, adjacent to the NTD, interfered with coactivation of ELK1, and residual ELK1 coactivation by the mutants was insensitive to KCI807. In a glutathione S-transferase pull-down assay, KCI807 inhibited ELK1 binding to an AR polypeptide that included the two ELK1 binding segments and the DBD but did not affect ELK1 binding to a similar AR segment that lacked the sequence downstream of residue 566. Raman spectroscopy detected KCI807-induced conformational change in the DBD. The data point to a putative KCI807 binding pocket within the crystal structure of the DBD and indicate that either mutations or binding of KCI807 at this site will induce conformational changes that disrupt ELK1 binding to the NTD.

Citation

Soave, C., Ducker, C., Islam, N., Kim, S., Yurgelevic, S., Nicely, N. I., …Ratnam, M. (2023). The Small Molecule Antagonist KCI807 Disrupts Association of the Amino-Terminal Domain of the Androgen Receptor with ELK1 by Modulating the Adjacent DNA Binding Domain. Molecular Pharmacology, 103(4), 211-220. https://doi.org/10.1124/molpharm.122.000589

Journal Article Type Article
Acceptance Date Dec 27, 2022
Online Publication Date Mar 16, 2023
Publication Date 2023-04
Deposit Date Jul 11, 2023
Publicly Available Date Jul 11, 2023
Journal Molecular Pharmacology
Print ISSN 0026-895X
Electronic ISSN 1521-0111
Publisher American Society for Pharmacology and Experimental Therapeutics
Peer Reviewed Peer Reviewed
Volume 103
Issue 4
Pages 211-220
DOI https://doi.org/10.1124/molpharm.122.000589
Keywords Pharmacology; Molecular Medicine
Public URL https://nottingham-repository.worktribe.com/output/22455164
Publisher URL https://molpharm.aspetjournals.org/content/103/4/211

Files





You might also like



Downloadable Citations