Recombinant expression and purification of heparin binding proteins: Midkine and pleiotrophin from Escherichia Coli

Midkine (MDK) and Pleiotrophin (pm) belong to a class of heparin-binding growth factors and are highly expressed in a number of cancers. Bioactive and recombinant MDK and PTN are critical reagent for cancer drug discovery studies. MDK and PTN belong to a newly evolving family of secreted neurotrophic and developmentally regulated heparin-binding molecules. PIN is related to MDK with 45% sequence identity and both proteins have been shown to be involved in promoting neurite outgrowth. MDK is a cysteine-rich 13 kDa protein containing five disulfide bonds and PIN is 19 kDa protein containing ten disulphide bonds. In this study, we expressed recombinant human MDK (rhMDK), mouse MDK (rmMDK) and human pleiotrophin (rhPTN) in Escherichia coli BL21(DE3)pLysS strain. Soluble rhMDK, rmMDK and rhPTN were expressed at a high-level in this strain and the protein was purified (similar to 90%) by a one-step purification using heparin affinity chromatography. A total of 4 mg purified MDK and 7 mg of purified PTN were obtained with the overall yield from 1 L of bacterial culture. Activity of purified rhMDK and rhPTN was confirmed by a cell proliferation assay using NIH3T3 cells. (C) 2012 Elsevier Inc. All rights reserved.