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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). |
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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