pwPICZalpha-DT390-bi-pIL-2-Gly

Protein Expression Eukaryotic cells - P. pastoris Porcine IL-2 fusion toxins

Experiment
Protein Expression Eukaryotic cells - P. pastoris Porcine IL-2 fusion toxins
Product
pwPICZalpha-DT390-bi-pIL-2-Gly from Zhirui Wang, Transplantation Biology Research Center, Massachuse
Manufacturer
Zhirui Wang, Transplantation Biology Research Center, Massachuse

Protocol tips

Protocol tips
Protein expression and purification in Pichia pastoris were performed as previously described with the following modifications (Wang et al., 2011; Peraino et al., 2012).
Downstream tips
A Ni-Sepharose fast flow resin (GE healthcare) was used for the purification. Porcine IL-2 fusion toxins were eluted using 40 mM imidazole. Western blot analysis, FACS analysis, FACS competition/blocking analysis and KD determination were all performed as previously described (Peraino et al., 2012) using LCL13271 cells (Cho et al., 2007).

Publication protocol

Protein expression and purification in Pichia pastoris were performed as previously described with the following modifications (Wang et al., 2011; Peraino et al., 2012). A Ni-Sepharose fast flow resin (GE healthcare) was used for the purification. Porcine IL-2 fusion toxins were eluted using 40 mM imidazole. Western blot analysis, FACS analysis, FACS competition/blocking analysis and KD determination were all performed as previously described (Peraino et al., 2012) using LCL13271 cells (Cho et al., 2007). The OntakĀ®-like monovalent human IL-2 fusion toxin (DT390-hIL-2) used as a control for our in vitro assay was constructed, expressed and purified exactly same as the monovalent porcine IL-2 fusion toxin. The DT390 alone and the non-N-glycosylated porcine IL-2 alone (pIL-2-Non-N-Gly) were used as controls for our in vitro assay. These products were also expressed and purified in the yeast Pichia Pastoris system.

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Manufacturer protocol

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