Production of recombinant human xCT (SLC7A11) and reconstitution in proteoliposomes for functional studies

The plasma membrane transporter xCT belongs to the SLC7 family and has the physiological role of mediating the exchange of glutamate and cystine across the cell plasma membrane, being crucial for redox control. The xCT protein forms a heterodimer with the ancillary protein CD98. Over the years, xCT...

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Published inFrontiers in physiology Vol. 13; p. 993626
Main Authors Galluccio, Michele, Scalise, Mariafrancesca, Pappacoda, Gilda, Scarpelli, Martina, Bonanomi, Marcella, Gaglio, Daniela, Indiveri, Cesare
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 06.09.2022
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Summary:The plasma membrane transporter xCT belongs to the SLC7 family and has the physiological role of mediating the exchange of glutamate and cystine across the cell plasma membrane, being crucial for redox control. The xCT protein forms a heterodimer with the ancillary protein CD98. Over the years, xCT became a hot pharmacological target due to the documented over-expression in virtually all human cancers, which rely on cystine availability for their progression. Notwithstanding, several unknown aspects of xCT biology still exist that require a suitable single protein experimental model, to be addressed. To this aim, the recombinant host Escherichia coli has been exploited to over-express the human isoform of xCT. In this widely used and low-cost system, the optimization for growth and protein production has been achieved by acting on the metabolic needs of the bacterial strains. Then, the His-tagged protein has been purified by Ni 2+ -chelating chromatography and reconstituted in proteoliposomes for transport activity assays. The expressed protein was in a folded/active state allowing functional and kinetic characterization. Interestingly, the features of the recombinant protein meet those of the native one extracted from intact cells, further confirming the suitability of E. coli as a host for the expression of human proteins. This study opens perspectives for elucidating other molecular aspects of xCT, as well as for studying the interaction with endogenous and exogenous compounds, relevant to human health.
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Sonja Sucic, Medical University of Vienna, Austria
Reviewed by: Lan Guan, Texas Tech University Health Sciences Center, United States
Edited by: Tiziano Verri, University of Salento, Italy
This article was submitted to Membrane Physiology and Membrane Biophysics, a section of the journal Frontiers in Physiology
ISSN:1664-042X
1664-042X
DOI:10.3389/fphys.2022.993626