Difference between revisions of "Part:BBa K320006:Experience"
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[[Image:EPFL Gel1 western.jpg|400px|thumb|center| '''Gel1 (Lysates):''' We can see distinctive molecular fragments in the immunotoxin lane: The upper fragments (marked with red and purple arrows) match the molecular size of the immunotoxin of about 39 kDa. For the shorter of the two fragments the export tag pelB may have been cut off. The smaller sized fragment (green arrow) of about 20 kDa is most likely part of the degraded immunotoxin. | [[Image:EPFL Gel1 western.jpg|400px|thumb|center| '''Gel1 (Lysates):''' We can see distinctive molecular fragments in the immunotoxin lane: The upper fragments (marked with red and purple arrows) match the molecular size of the immunotoxin of about 39 kDa. For the shorter of the two fragments the export tag pelB may have been cut off. The smaller sized fragment (green arrow) of about 20 kDa is most likely part of the degraded immunotoxin. | ||
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'''Gel2 (Supernatants):''' A fragment of the correct size is detected in the supernatant. The smaller fragments (green and yellow arrows) probably correspond to smaller parts of the degraded immunotoxin. ]] | '''Gel2 (Supernatants):''' A fragment of the correct size is detected in the supernatant. The smaller fragments (green and yellow arrows) probably correspond to smaller parts of the degraded immunotoxin. ]] | ||
Revision as of 12:03, 27 October 2010
The Immunotoxin is expressed and appears in the supernatant
We tested expression of the immunotoxin in E. coli (see [http://2010.igem.org/wiki/index.php?title=Team:EPF_Lausanne/Project/Materials_Methods Materials and Methods] for details). In a western blot analysis of whole cell lysates we were able to see bands corresponding to full length immunotoxin and possibly degraded fragments of the protein (see figure). The immunotoxin contains a PelB sequence that targets it for secretion into the periplasm. We concentrated the supernatant of both the immunotoxin and a control culture by running it through a filtering device with a 5 kDa cut-off. Running a western blot with these samples (see figure) we could show that the immunotoxin was found in the supernatant as expected.
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