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Resolution: standard / high Figure 2.
DBL2-X and DBL3-X expression in E. coli and purification. a. Electrophoresis in an SDS 12% polyacrylamide gel of aliquots from different steps
in expression, refolding and purification of DBL3-X. Lane 1, non-induced BL21 (DE3)
(containing pET24a-DBL3-X plasmid); lane 2, induced BL21 (DE3) containing the pET24a-DBL3-X
plasmid; lane 3, inclusion bodies suspension; lane 4, inclusion bodies after washing
and denaturation in Urea 8 M; lane 5, affinity column flow through; lane 6, portion
of DBL3-X lost during refolding onto the affinity column; lane 7, affinity column
elution pool; lane 8, molecular size exclusion column purified DBL3-X. b. Electrophoresis
of refolded DBL3-X in a SDS 12% polyacrylamide gel before (-) and after (+) reduction
with dithiothreitol (DTT). c. Electrophoresis of refolded DBL2-X in a SDS 12% polyacrylamide
gel before (-) and after (+) reduction with dithiothreitol (DTT). Higher mobility
before reduction indicates the presence of disulfide linkages.
Fernandez et al. Malaria Journal 2008 7:170 doi:10.1186/1475-2875-7-170 |