Functional Expression of Multidrug Resistance Protein 4 MRP4/ABCC4. (December 2019)

• Record Type: Journal Article
• Authors: Hardy, David; Bill, Roslyn M.; Jawhari, Anass; Rothnie, Alice J.
• Is Part Of: SLAS discovery. Volume 24:Number 10(2019)
• Page Start: 1000
• Page End: 1008
• Publication Date: 2019-12
• Subjects: ABC transporter -- membrane protein expression -- fluorescence -- vesicular transport assay; Drugs -- Analysis -- Periodicals; Drugs -- Testing -- Periodicals; Biomolecules -- Analysis -- Periodicals; Biomolecules -- Analysis; Drugs -- Analysis; Drugs -- Testing; Drug Evaluation, Preclinical; Molecular Biology -- methods; Periodicals; Periodicals; 615.1
• DOI: 10.1177/2472555219867070
• Languages: English
• ISSNs: 2472-5552

Abstract

To study the function and structure of membrane proteins, high quantities of pure and stable protein are needed. One of the first hurdles in accomplishing this is expression of the membrane protein at high levels and in a functional state. Membrane proteins are naturally expressed at low levels, so finding a suitable host for overexpression is imperative. Multidrug resistance protein 4 (MRP4) or ATP-binding cassette subfamily C member 4 (ABCC4) is a multi-transmembrane protein that is able to transport a range of organic anionic compounds (both endogenous and xenobiotic) out of the cell. This versatile transporter has been linked with extracellular signaling pathways and cellular protection, along with conferring drug resistance in cancers. Here we report the use of MRP4 as a case study to be expressed in three different expression systems: mammalian, insect, and yeast cells, to gain the highest yield possible. Interestingly, using the baculovirus expression system with Sf 9 insect cells produced the highest protein yields. Vesicular transport assays were used to confirm that MRP4 expressed in Sf 9 was functional using a fluorescent cAMP analogue (fluo-cAMP) instead of the traditional radiolabeled substrates. MRP4 transported fluo-cAMP in an ATP-dependent manner. The specificity of functional expression of MRP4 was validated by the use of nonhydrolyzable ATP analogues and MRP4 inhibitor MK571. Functionally expressed MRP4 in Sf 9 cells can now be used in downstream processes such as solubilization and purification in order to better understand its function and structure.