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Updated: Jul 14, 2026

Overexpression and Purification of Human Cis-prenyltransferase in Escherichia coli
Published on: August 3, 2017
Expression and purification in high yield of a functionally active recombinant human Type I inositol(1,4,5)P3
Alexandre Wohlkönig1, Magalie Sénéchal, Frédérique Dewitte
1UMR8161, Institut de Biologie de Lille, CNRS/Université de Lille1/Université de Lille2/Institut Pasteur de Lille, IFR 142, 1 rue du Professeur Calmette, Lille 59021, France. alexandre.wohlkonig@ibl.fr
Abstract:
Inositol polyphosphates are the most widespread second messenger molecules in eukaryotic cells. Human Type I inositol 1,4,5-triphosphate (Ins(1,4,5)P(3)) 5-phosphatase removes the D-5 position phosphate from soluble Ins(1,4,5)P(3,) a key event in cell signaling particularly in Ca(2+) homeostasis. In this study, the cDNA encoding human Type I Ins(1,4,5)P(3) 5-phosphatase was subcloned into a modified pMAL expression vector. This plasmid produces a recombinant protein in fusion with affinity tags located at its N-terminus, consisting in a maltose binding protein (MPB) and an octa-histidine stretch. The construction was transformed into Escherichia coli BL21 (DE3) expression strain. This dual tag strategy allows the purification of milligrams of highly purified protein. The recombinant human Type I Ins(1,4,5)P(3) 5-phosphatase is active and can thus be used for functional and structural studies.
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