Part:BBa_K3813000
Mucin(MUC 1) with optimized TA promoter and Lux terminator
Part Info
This part can be used to initiate the production of the Mucin 1 biomarker(protein) in an E.Coli cell system. Mucin 1 is an essential biomarker that is beneficial towards the detection of breast cancer. We decided to synthesize Mucin 1 in E.Coli in order to model biomarkers in human breast tissue and apply this for our aptamer experiments.
Construct Design
This is a composite part made up of a combination of previously existing parts from the iGEM registry: optimized (TA) repeat constitutive promoter with 13 bp between -10 and -35 elements(BBa_K137085) and LuxICDABEG terminator(BBa_B0011), RBS along with the Mucin 1 gene sequence from NCBI.
Results
We selected the forward and reverse primers for our Mucin protein sequence.
MUC-1: Forward primer GTGCCCCCTAGCAGTACCG Reverse primer GACGTGCCCCTACAAGTTGG
We first used PCR to amplify our protein-coding sequence(found on NCBI) and selected our forward and reverse primers based on an extensive literature review we performed.
We then used Gibson Assembly to construct our part in the iGEM chloramphenicol backbone pSB1C3, before transforming it into E.Coli cells. We used a GFP reporter in our construct to monitor if the Mucin sequence was successfully expressed in our E.Coli cells. Following transformation, we first qualitatively analyzed the plates to see if they were glowing. Since our construct was tagged with GFP, if the biomarker was successfully produced, then our colonies would glow.
Our qualitative analysis observed that there were glowing colonies on all parts of the plate, with relatively large colonies.
Figure 1: Transformation Results for BBa K3813000. The glowing colonies seen in the picture represent that Mucin was successfully expressed in the system and that we could quantitatively analyze for the amount of protein produced through purification.
Protein Expression and Purification
To further verify our findings, we purified the Mucin that was produced through transformation by applying freezing/cracking before using the regular purification process. This was because the Mucin sequence was relatively large and without a tag, it was difficult to extract the protein out through regular purification. PAGE electrophoresis and readings from the 96-well plate reader indicated the presence of Mucin from this construct.
Analysis of Protein Concentration
To calculate the concentrations of the biomarkers within each well, we first ran the BSA model to create the standard curve, where the x-axis represents absorbance, and y-axis represents the concentration in mg/ml. The standard curve later allowed us to convert the measured absorbance into measurements of concentration. The equation and the image of the standard graph we derived from the BSA model is as follows.
Figure 2: Standard Curve for BSA
Using the standard curve and the measured absorbance, we interpolated values of concentration for each of the different constructs. We performed this conversion by substituting the absorbance values into the x-variable in our standard curve, to find the corresponding y-variable which represents concentration. The post-conversion concentrations of the biomarkers are listed below.
For construct BBa_K3813001, we had a reading of 0.26 mg/ml for the concentration of biomarker synthesized. Compared to other constructs, the yield of biomarker synthesized is relatively low, but the results indicate that Mucin was successfully synthesized and expressed in our E.Coli system.
References
[1] Wang, Y., Kirpich, I., Liu, Y., Ma, Z., Barve, S., McClain, C. J., & Feng, W. (2011). Lactobacillus rhamnosus GG treatment potentiates intestinal hypoxia-inducible factor, promotes intestinal integrity and ameliorates alcohol-induced liver injury. The American Journal of Pathology, 179(6), 2866–2875.
[2]Homo sapiens chromosome 1, GRCh38.p13 Primary Assembly - Nucleotide - NCBI. (n.d.). Retrieved August 2, 2021, from https://www.ncbi.nlm.nih.gov/nuccore/NC_000001.11?report=fasta&from=155185824&to=155192915&strand=true
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 26
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1913
Illegal NgoMIV site found at 1973
Illegal NgoMIV site found at 2032
Illegal NgoMIV site found at 2087
Illegal NgoMIV site found at 2122
Illegal NgoMIV site found at 2182
Illegal NgoMIV site found at 2362 - 1000COMPATIBLE WITH RFC[1000]
| None |