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Team:Calgary/Sandbox/Notebook/Journal/Linker
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<p><b>Figure 5.</b> Confirmation digests of the K-coil, E-coil with His-tag and the E-coil parts within the pUC57 vector using the NotI enzyme. Bands are all expected to be approximately 100-bp and are indicated by the orange arrows due to their faintness. The –C lane is a negative control. +C indicates a positive control making use of the RFP coding device J04450 which has an expected size of about 1100-bp when digested. The gel was a 2% agarose gel and was run at 80 volts for 90 minutes.</p> | <p><b>Figure 5.</b> Confirmation digests of the K-coil, E-coil with His-tag and the E-coil parts within the pUC57 vector using the NotI enzyme. Bands are all expected to be approximately 100-bp and are indicated by the orange arrows due to their faintness. The –C lane is a negative control. +C indicates a positive control making use of the RFP coding device J04450 which has an expected size of about 1100-bp when digested. The gel was a 2% agarose gel and was run at 80 volts for 90 minutes.</p> | ||
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Revision as of 18:57, 16 September 2013
Linker Journal
Week 1: May 1 - May 3
This week we attended the appropriate safety courses required by our University to work in the lab. Besides that, the undergraduate supervisors presented about the principles of Genetics and Synthetic Biology to the new team members.
Week 2: May 6 - May 10
This week we participated in a general molecular biology workshop to refresh our memory of techniques used in molecular biology.
Week 3: May 13 - May 17
We continued the molecular biology workshop. This week we also divided up into our respective groups for the project and decided research priorities.
Week 4: May 20 - May 24
This week we started to perform literature searches for our element of the project. Our goal is to find a way to link the transcription activator-like effector (TALE) and ferritin elements of the project. We have decided that using a two part system is optimal as this would allow the ferritin subunits to self-assemble without having a TALE protein attached that could potentially interfere with this process. In order to accomplish this we have decided to use coiled-coils. The synthetic IAAL E3 and IAAL K3 coils (Litowski and Hodges, 2002) have been selected to accomplish this. These coils make use of hydrophobic regions composed of leucine and isoleucine to bind to each other (Figure 1). The specificity of these coils is conveyed by the presence of glutamic acid and lysine residue that limit the binding to the formation of coil heterodimers.
Figure 1. A helical wheel representation of the IAAL E3/K3 coiled-coil heterodimer viewed as a cross-section based off of a similar figure created by Litowski and Hodges (2002). The peptide chain propagates into the page from the N to the C terminus. Hydrophobic interactions between the coils are indicated by the clear wide arrows. The intermolecular electrostatic interactions between the coils are displayed by the thin curved arrow (eg. Between Glu15 and Lys20).
Based off of results from previous ferritin fusions (Kim et al., 2011) it was decided that a linker sequence was needed between the coils and their respective proteins to prevent any steric hindrance due to the size of the ferritin and TALE proteins. A flexible glycine rich linker lacking protease cut sites was selected from the registry (BBa_K157013)
Week 5: May 27 - May 31
We continued to perform literature searches this week for our project. This week our main focus was on determining ways we could characterize our coils and finding additional useful properties of coils. Many papers make use of circular dichroism in order to detect if the coils are able to bind to each other. This technique requires the use of a spectropolarimeter and a fair amount of knowledge to complete so it may not be the most ideal technique in our situation given the timelines we are working on. Another option consists of using FRET (Förster resonance energy transfer) to measure the binding of the coils. The idea is to have an individual fluorophore attached to each coil so that when the coils are bound the process of FRET can occur and light emission will be observed from the fluorescent protein that is having energy being transferred to it from the other fluorescent protein (Apostolovic and Klok, 2008). This technique can be difficult to perform however so it will likely be maintained as a backup characterization technique.
One interesting properties of coils is that they are sensitive to acidic pH levels (Apostolovic and Klok, 2008). This warrants examination once we have our coils complete and purified as a protein as this pH sensitivity could be problematic for our system or it may act as a benefit.
Week 6: June 3 - June 7
Based on the research we have done in the previous weeks we have decided to plot out some experiments that will help us characterize our coils. We plan make use of a Ni-NTA column and His-tags on our coils to characterize our coils. The idea is that we can have a His-tag located on one of the coils and this coil will bind to the column via the His-tag. The second coil will be fused to protein such as GFP (BBa_K648013). This second coil will not have a His-tag and when passed through the column it ideally should bind to the other coil already immobilized via a His-tag. By varying the conditions within the column we should be able to characterize the binding of the coils. If the coil fused to GFP falls off of the other coil it should be located in the collected fluid. The presence of the GFP can be detected by both fluorescence and SDS-PAGE.
Three proposed experiments that we have making use of this are detailed below:
- The first test will just test the binding of the coils to each other under standard coil binding conditions (pH = 7). A K-coil will be bound to a drip Ni-NTA column via a 6x His-tag C-terminus fusion. An E-coil with an N-terminus GFP fusion can then interact with the K-coil that is bound to the column. If the interaction is successful the GFP will not be found in high quantities in the wash steps. The GFP fusion should elute when imidazole is added to the column. The levels of GFP can be verified using both emission measurements and SDS-PAGE.
- The second test will make use of this column but will measure the effect of pH on the binding of the coils. Different columns will be set up with different pH washes (3, 5, 7 and 9). It has been previously reported that the coils begin to dissociate at a pH of 5 (Apostolovic and Klok, 2008).
- The third test will make use of a spin Ni-NTA column. This test will testthe ability of the heterodimer coiled-coils to resist shearing due to applied forces. The columns will undergo centrifugation at different steps after the proteins have been bound to determine if the forces present have any effect on the binding of the coils.
Week 7: June 10 - June 14
This week involved transforming the part BBa_K648013 received by request from the Registry of Standard Biological Parts. This part is a GFP reporter that contains the RFC 25 standard prefix and suffix. This prefix and suffix will allow us to create a fusion protein with GFP and the coils to be used in our testing purposes. After successful transformation of the part the plasmid was isolated via miniprep and its presence was confirmed through a restriction digest. The part was also sequence confirmed to indeed verify that there were no unexpected changes to the nucleotide sequence.
Week 8: June 17 - June 21
Research efforts were devoted to the Ferritin system during this week. Flooding in the city of Calgary interrupted the planned lab work for the beta-lactamase and coil group.
Week 9: June 24 - June 28
The first BioBrick construction was attempted this week. The goal was to put the RFC25 fusion standard GFP (BBa_K648013) behind the IPTG inducible LacI promoter (with a ribosome binding site) (BBa_J04500). This construction however did not yield any colonies after ligation and transformation were performed. It is recommended the next time this construction be performed that the amount of vector DNA added to the ligation reaction be increased from 5 µL to 7 µL to correct for the dilution of the vector DNA during the Antarctic phosphatase treatment performed. BBa_J04500 in pSB1C3 was transformed this week so that we could have this part available with a chloramphenicol resistant plasmid. The colony PCR for this part was successful (Figure 3) ergo overnight cultures were prepared on the weekend so that a miniprep of the plasmid could be performed the next week.
Figure 3. A colony PCR of potential colonies containing the part J04500. Standard BioBrick primers were used. Bands between 400 and 500-bp indicate the successful amplification of these parts. +C indicates a positive control making use of the RFP coding device J04450 which has an expected size of about 1300-bp when using BioBrick primers. Some non-specific amplification is seen within this control. The gel was 1% agarose and was run at 100 V for an hour.
Week 10: July 1 - July 5
The overnight cultures produced on the weekend were successfully miniprepped producing DNA stocks of the LacI promoter BBa_J04500 (in pSB1C3). Restriction digests of this part confirmed a successful transformation and miniprep. An initial attempt was made to make a construct composed of the LacI promoter BBa_J04500 followed by the RFC25 fusion standard GFP (BBa_K648013). This construction produced few viable colonies. One colony appeared to have the expected band size after colony PCR (Figure 4) however this result could not be replicated. This construction will be attempted again in the future.
Figure 4. A colony PCR of potential colonies containing the part J04500 + K648013. Standard BioBrick primers were used. The band about 1100-bp in size indicates the successful amplification of this part. +C indicates a positive control making use of the RFP coding device J04450 which has an expected size of about 1300-bp when using BioBrick primers. No contamination is observed in the NTC (no template control). The gel was 1% agarose and was run at 100 V for an hour.
Also received this week were the synthesized coil genes ordered from BioBasic. These genes are the K-coil, E-coil, K-coil with a His-tag, and E-coil with a His-tag. These genes were successfully transformed into our E. coli cells and were miniprepped successfully. These genes are in the pUC57 (pUC57 PDF Information Sheet) vector and will have to be plasmid switched into pSB1C3 for submission to the registry.
Week 11: July 8 - July 12
Confirmation digests were performed upon the coil parts miniprepped last week in order to confirm the presence of the coils (Figures 5). These coils can be seen as the faint bands at approximately 100-bp in size on the gel. Digestions like these could be performed as the synthesized genes contain the RFC 25 prefix and suffix. These digestions revealed that the coil genes are indeed present in the minipreps produced. Glycerol stocks were made of our transformed cells for organized long term storage.
Figure 5. Confirmation digests of the K-coil, E-coil with His-tag and the E-coil parts within the pUC57 vector using the NotI enzyme. Bands are all expected to be approximately 100-bp and are indicated by the orange arrows due to their faintness. The –C lane is a negative control. +C indicates a positive control making use of the RFP coding device J04450 which has an expected size of about 1100-bp when digested. The gel was a 2% agarose gel and was run at 80 volts for 90 minutes.
Several constructions were attempted this week. These constructions consist of placing the beta-lactmase gene with a His-tag behind the promoter BBa_J04500 and the RFC25 fusion standard GFP (BBa_K648013) behind the same promoter. Also attempted were plasmid switches of all of the coil genes ordered as well as the three beta-lactamase genes extracted via PCR. Colonies were seen for all of the transformed ligation mixtures for these constructions. Colony PCR of these transformed colonies only produced potentially viable results for the J04500 + K648013, and J04500 + Beta-lactamase (with His-tag) constructs. The K-coil, K-coil His-tag and E-coil His-tag plasmid switches also displayed bands around the expected size during colony PCR.
Week 12: July 15 - July 19
This week contained some disappointment as the BioBrick constructions continued to have limited efficacy. The confirmation digests of the constructs that showed some promise during last week’s colony PCR (J04500 + K648013, J04500 + Beta-lactamase with a His-tag) and the plasmid switches (K-coil, K-coil His-tag and E-coil His-tag) did not produce expected results. One rather notable issue is the ~200-bp size difference seen in the J04500 + K648013 from the expected size of 955-bp. The difference appears to suggest that the LacI promoter is not present. This hypothesis was confirmed with sequencing results. This would suggest that the wrong enzymes were used during construction or that there is potential contamination of the enzyme buffers used.
A replicate of these constructions this week also produced similar results. Due to this it is recommended that new buffers be used for further constructions. Some of the difficulty present with plasmid switching the coils is due to their small size however. Since the coils themselves are at minimum approximately 60-bp in size. This is not kinetically favorable for BioBrick construction. It may be wise to primer on the coils to appropriate constructs when the time comes for their addition. Also present in our constructions are re-ligations of the original vector. Due to this the time for phosphatase treatment will be increased from two to three hours to limit this issue. The second construction from this week however did produce a construction that appeared to be the J04500 + Beta-lactamase with a His-tag part. This construction was sent in for sequencing over the weekend.
Week 13: July 22 - July 26
Proceeding with the recommendations from last week regarding BioBrick constructions the J04500 + Beta-lactamase with a His-tag construction and plasmid switches of the beta-lactamase and coil genes into pSB1C3. Based off of the colony PCR there were some potential completed parts for the plasmid switches. Verification digests of the miniprepped plasmids from these colonies combined with sequencing revealed the successful plasmid switch of the beta-lactamase gene with a His-tag at the C-terminus, the beta-lactamase gene with a glycine linker at the N-terminus and the E-coil with a His-tag (Figure 8).
Figure 8. Confirmation digests of the K-coil, E-coil with His-tag, K-coil with His-tag and the E-coil parts within the pUC57 vector using the NotI enzyme are present in the respectively labelled lanes. These digests were used to confirm if older coil stocks were suitable for construction. Also present are the confirmation digests of the K-coil, E-coil with His-tag, and K-coil with His-tag after an attempted plasmid switch into pSB1C3. The expected bands were observed for the plasmid switch of the E-coil with the His-tag. Due to the faintness of the bands they are indicated with orange arrows (reference stock plasmid bands are also indicated). Positive and negative control lanes are present on another gel. The gel was a 2% agarose gel and was run at 80 volts for 90 minutes.
The J04500 + Beta-lactamase with a His-tag construction started this week was not pursued further as sequencing revealed that a construction from last week had indeed produced this part. Mutagenesis primers were designed for this gene as a BsaI cut site is present in the sequence which could interfere with any Golden Gate assembly attempted with this part. Successful mutation of this part was completed and confirmed via gel electrophoresis and sequencing. A preliminary test was also attempted with this part in order to see if the leaky properties of the LacI (BBa_J04500) promoter could successfully produce beta-lactamase at levels large enough to allow the transformed cells to survive on plates containing ampicillin even though this part exists in a chloramphenicol resistant plasmid (pSB1C3). This test successfully displayed that active beta-lactamase was being produced by our cells.
Week 14: July 29 - August 2
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Week 15: August 5 - August 9
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Week 16: August 12 - August 16
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Week 17: August 19 - August 23
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Week 18: August 26 - August 30
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Week 19: September 2 - September 6
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Week 20: September 9 - September 13
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Week 21: September 16 - September 20
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Week 22: September 23 - September 27
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Week 23: September 30 - October 4
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