Part:BBa_K1590001
Human Haemoglobin B
Human haemoglobin (hemoglobin) forms a tetramer consisting of two A-chains and two B-chains. This biobrick is a synthetic gene encoding the human haemoglobin B-chain that has been optimized for expression in E. coli.
Usage and Biology
Haemoglobin is the tetrameric protein molecule in red blood cells that carries oxygen. It is composed of four polypeptide chains, which in adults consist of two alpha (A) globin chains and two beta (B) globin chains. The protein also normally contains the iron-containing cofactor haem (or heme). Haemoglobin can still be found free in the blood plasma at a concentration of up to 0.1 g/l.
|
••••
iGEM Dundee 2015 |
This synthetic gene was found to produce stable product when expressed in E. coli cells. |
Results
Overexpression and Purification of Haemoglobin Beta
Initial experiments were carried out to optimise expression of haemoglobin beta (hHBB) within our E.coli chassis. The synthetic gene was subcloned into the pQE80-L overexpression vector that adds an N-terminal hexa-histidine tag onto the N-terminus of the protein. We found the following to be the optimum conditions:
We subcultured 50 µl of an overnight culture into fresh LB containing the appropriate antibiotics and grew the cells at 37C until an OD-600 of ~0.6 was reached. The production of protein was then induced by adding 1 mM (final concentration)of IPTG then the cells were grown for a further 3 hours at 37C. Next, 1 ml of this culture was then taken for analysis by western immunblot which showed that haemoglobin beta was successfully overexpressed (Figure 1).
- Figure 1: Western analysis of Human Haemoglobin B production in E. coli.
Purification of haemoglobin beta<b>
This was then scaled up and 4 litres of E.coli containing pQE80-L hHBB was grown for purification of haemoglobin beta by nickel affinity FPLC (fast liquid chromatography). The optimum conditions for this were as follows: 4 x 1L of fresh LB growth medium containing ampicillin and kanamycin was inoculated with 50ml of haemoglobin beta overnight culture and left to grow until an OD600 of between 0.6-1 at 37oC. The expression of protein was then induced by adding 1mM of IPTG then the cells were grown for a further 6 hours at 20oC. Using FPLC, the supernatant was loaded onto a nickel column and the protein was eluted using an increasing concentration of imidazole. The results from this can be seen in Figure 2.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
| None |