Stabilization of human Multidrug Resistance Protein 4 (MRP4/ABCC4) using novel solubilization agents.

Hardy, David, Bill, Roslyn M, Rothnie, Alice J and Jawhari, Anass (2019). Stabilization of human Multidrug Resistance Protein 4 (MRP4/ABCC4) using novel solubilization agents. SLAS Discovery ,

Abstract

Membrane proteins (MP) are important drug discovery targets for a wide range of diseases. However, elucidating the structure and function of native MP is notoriously challenging as their original structure has to be maintained once removed from the lipid bilayer. Conventionally detergents have been used to solubilize MP with varying degrees of success concerning MP stability. To try to address this, new more stabilizing agents have been developed such as calixarene-based detergents and styrene maleic acid co-polymer (SMA). Calixarene based detergents exhibit enhanced solubilizing and stabilizing properties compared to conventional detergents, whereas SMA is able to extract membrane proteins with their surrounding lipids forming a nanodisc structure. Here we report a comparative study using classical detergents, calixarene based detergents and SMA to assess the solubilization and stabilization of the human ABC transporter MRP4 (multidrug resistance protein 4/ABCC4). We show that both SMA and calixarene based detergents have a higher solubility efficiency (at least 80%) than conventional detergents and show striking overstabilization features of MRP4 (up to 70°C) with at least 30°C stability improvement in comparison to the best conventional detergents. These solubilizing agents were successfully used to purify aggregate free homogenous and stable MRP4, with 7-fold higher yield for C4C7 Calixarene detergent in comparison to SMA. This work paves the way to MRP4 structural and functional investigations and illustrates once more the high value of using Calixarene based detergent or SMA as versatile and efficient tools to study MP and eventually enable drug discovery of challenging and highly druggable targets.

Publication DOI: https://doi.org/10.1177/2472555219867074
Divisions: Life & Health Sciences > Biosciences
Life & Health Sciences > Cellular and Molecular Biomedicine
Life & Health Sciences
Additional Information: © Sage 2019. The final publication is available via Sage at http://dx.doi.org/10.1177/2472555219867074
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Related URLs: https://journal ... cr_pub%3dpubmed (Publisher URL)
Accepted Date: 2019-07-10
Published Online Date: 2019-08-05
Authors: Hardy, David
Bill, Roslyn M ( 0000-0003-1331-0852)
Rothnie, Alice J ( 0000-0002-4259-7015)
Jawhari, Anass

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