Ion mobility mass spectrometry unveils conformational effects of drug lead EPI‐001 on the intrinsically disordered N‐terminal domain of the androgen receptor

• Published in: Protein science 2024-12, Vol.34 (1)
• Main Authors: Ahmed, Ikhlas M. M., Rofe, Adam, Henry, Martyn C., West, Eric, Jamieson, Craig, McEwan, Iain J., Beveridge, Rebecca
• Format: Article
• Language: English
• ISSN: 0961-8368; 1469-896X
• DOI: 10.1002/pro.5254

Intrinsically disordered proteins (IDPs) are important drug targets as they are key actors within cell signaling networks. However, the conformational plasticity of IDPs renders them challenging to characterize, which is a bottleneck in developing small molecule drugs that bind to IDPs and modulate their behavior. In relation to this, ion mobility mass spectrometry (IM‐MS) is a useful tool to investigate IDPs, as it can reveal their conformational preferences. It can also offer important insights in drug discovery, as it can measure binding stoichiometry and unveil conformational shifts of IDPs exerted by the binding of small drug‐like molecules. Herein, we have used IM‐MS to investigate the effect of drug lead EPI‐001 on the disordered N ‐terminal domain of the androgen receptor (AR‐NTD). Despite structural heterogeneity rendering the NTD a challenging region of the protein to drug, this domain harbors most, if not all, of the transcriptional activity. We quantify the stoichiometry of EPI‐001 binding to various constructs corresponding to functional domains of AR‐NTD and show that it binds to separate constructs containing transactivation unit (TAU)‐1 and TAU‐5, respectively, and that 1–2 molecules bind to a larger construct containing both sequences. We also identify a conformational shift upon EPI‐001 binding to the TAU‐5, and to a much lesser extent with TAU‐1 containing constructs. This work provides novel insight on the interactions of EPI‐001 with the AR‐NTD, and the structural alterations that it exerts, and positions IM‐MS as an informative tool that will enhance the tractability of IDPs, potentially leading to better therapies.