Team:Yale/MaterialsMethods
From 2014.igem.org
Line 299: | Line 299: | ||
</p> <br> | </p> <br> | ||
- | <center><img src ="https://static.igem.org/mediawiki/2014/thumb/3/33/Purification2014.png/400px-Purification2014.png" height = "500" width = "auto"></img><br/><i><strong>Figure 3. </strong>A diagram illustrating the proposed purification method.</i></center> | + | <center><img src ="https://static.igem.org/mediawiki/2014/thumb/3/33/Purification2014.png/400px-Purification2014.png" height = "500" width = "auto"></img><br><br/><i><strong>Figure 3. </strong>A diagram illustrating the proposed purification method.</i></center> |
</div> | </div> |
Revision as of 02:20, 18 October 2014
Materials and Methods |
|||||||||||
T7 Riboregulation SystemStrains, Plasmids, and Reagents E. coli strains used in this study included BL21(E. coli B F- dcm ompT hsdS(rB- mB-) gal [malB+]K-12 (λS)), BL21(DE3)( F– ompT gal dcm lon hsdSB(rB- mB-) λ(DE3 [lacI lacUV5-T7 gene 1 ind1 sam7 nin5])), ECNR2(ΔmutS:cat.Δ(ybhB-bioAB): [λcI857.Δ(cro-ea59):tetR-bla]), and Mach1(ΔrecA1398 endA1 tonA Φ80ΔlacM15 ΔlacX74 hsdR(r K- mK+). Strains used for transformation were grown in LB Lennox(Cold Spring Harbor Protocols2006). Cells used for cloning and mini-prep were grown in selective medium of 2XYT (2xYt Medium (7281) 2010) with either kanamycin (American Bioanalytical) or spectinomycin (Sigma-Aldrich). Kanamycin and spectinomycin were used at 30 mg/mL and 95 mg/mL respectively. One percent agarose gels were made with 0.5% TBE obtained from American Bio and stained with either ethidium bromide (Sigma-Aldrich) (screening) or SYBR Safe (Invitrogen) (cloning) in the case of cloning. Gel extraction and purification was completed with QIAprep Gel Extraction Kit following the protocol provided. PCR purification was accomplished with the QIAquick PCR Purification Kit, following the protocol provided. Plasmid purification was accomplished using the QIAprep Spin Miniprep Kit and the protocol provided. For all DNA kits provided by QIAgen we used Denville Spin Columns for Nucleic Acid Purification. The concentration of DNA was measured using a Biotek Synergy HT Multi-Mode microplate Reader with accompanying Take3 Microvolume plates. All restriction enzymes, and Gibson Assembly Master Mix are from New England Biolabs. Hifi HotStart Readymix and 2GFAST Readymix with loading dye for PCR were obtained from KAPA Biosystems. Plasmids Plasmid pZE21_Y12_a12C_c contains a ColE1 origin of replication and a kanamycin resistance marker. At the multiple cloning site in the reverse direction is inserted a trans-activating RNA (taRNA) sequence expressed by PLtetO promoter and in the forward direction is a chloramphenicol resistance marker with a cis-repressing RNA (crRNA) on the 5’ UTR upstream of the ribosomal binding site(RBS). Plasmid pZE21::sfGFP also contains a ColE1 origin of replication and kanamycin resistance marker. Superfolder GFP (sfGFP) is inserted into the multiple cloning site and is expressed by PLtetO. pZA21_tRNA_TAGG has a p15a origin of replication and a spectinomycin resistance marker. In its multiple cloning site it contains a 3 Tyrosine ELP purification tag adjacent to GFP. The recombinant protein expression is driven by PLtetO. Gibson Assembly of plasmids from PCR products Fragments were assembled into plasmids using Gibson Assembly (Gibson, Young et al. 2009). Gel purified PCR products with 5’ complimentary overhangs were combined in equimolar ratios with ten microliters of Gibson Assembly Master Mix and additional nuclease free water to obtain a reaction volume of twenty microliters. The reaction was carried out in a thermocycler held constant at 50°C over the course of one hour. Transformation of Plasmids through Electroporation Transformation was carried out through electroporation. First, the plasmid to be transformed was desalted for an hour using a Millipore (type VSWP) drop dialysis film with 0.025 μm on ultra-pure Milli-Q water. One mL of liquid culture was centrifuged and washed twice with Milli-Q water. After washing, the cells were pelleted, the supernatant was removed, and the pellet was re-suspended in 50 μL of a dilute solution of DNA and nuclease free water (American Bioanalytical). The cells and DNA solutions were transferred to a Bio Rad 0.1 cm gap Gene Pulser cuvettes for electroporation and kept chilled. Electroporation was conducted with a Bio-Rad Gene Pulser Xcell Electroporator set to 1800 V, 25 μF, and 200 Ω. After electroporation, the cells were immediately transferred to 1 mL of LB Lennox and placed in a 37° incubator to recover for an hour. The cells were then plated on LB Lennox agar with an antibiotic selection factor for the transformed plasmid vector. Assembly of T7 RNA Polymerase in pZE21_Y12_a12C backbone The plasmid pZE21_Y12_a12C_T7RNAPol was Gibson Assembled from the T7 RNA Polymerase gene obtained from BL21(DE3) and the pZE_Y12_a12C backbone. The T7 RNA Polymerase gene was obtained from BL21(DE3) through colony PCR with primers pZE21_T7_F and pZE21_T7_R that anneal at either end of the T7 RNA Polymerase gene and include complimentary base pair overhangs on the 5’ end to pZE21_Y12_a12C at the site for assembly. PCR was completed on a Bio-Rad c1000 thermo cycler with KAPA Biosystems Hifi Hotstart Readymix following the KAPA Biosystems protocol. It was programmed for an annealing temperature at 58°C and an annealing time of 00:02:30. After PCR the reaction mixture was treated with Dpn1 restriction enzyme for 1 hour at 37°C to digest template DNA. The linear fragment was run on a 2% agarose gel stained with SYBR Safe, excised, and gel purified. pZE_Y12_a12C was obtained as a plasmid, transformed into Mach1 cells for cloning, and purified from liquid culture via mini-prep. The plasmid backbone was amplified with primers pZgib-F and a12gib-r. The reaction was carried out in Kapa Hifi Hotsart Readymix following the Kapa Biosystems protocol. The annealing temperature of the reaction was 58°C and the extension time was 00:02:30. The reaction mixture was treated with Dpn1 to digest template DNA and then run on a 1% agarose gel stained with SYBR Green. The linear fragment was excised and gel purified. Following this, 4000 ng of the linearized backbone was treated with a single digest with KpnI restriction enzyme, following the NEB protocol to remove the chloramphenicol resistance marker overhang from the reverse site. The reaction was carried out at 37°C for four hours in a Bio-rad c1000 thermocycler. The reaction mixture was PCR purified with the QIAquick PCR Purification Kit to yield a linear fragment of the desired backbone vector. Concentration of the DNA was obtained using the plate reader. The two fragments were assembled with New England Biolabs 2X Gibson Assembly Master Mix following the NEB Protocol. The resulting plasmid was drop dialyzed for one hour using Millipore drop dialysis filter paper and Milli-Q water. One μL of desalted DNA was diluted in 49 μL of nuclease free water and used for transformation into Mach1 Cells. Cells were plated on Lb Lennox agar with kanamycin and allowed to grow overnight in a 37°C incubator. A dozen colonies were selected for screening. The initial screening with colony PCR was completed with primers pz-integration-f and pz-integration-r and K2G FAST Readymix with loading dye following the protocol from Kapa Biosystems. The annealing temperature for the reaction was 58°C and the annealing time given was 0:03:30. The reaction mixture was treated with Dpn1 for one hour to eliminate template DNA and run on a 1% agarose gel stained with ethidium bromide for 30 minutes at 140V. The gel was imaged on a Bio-Rad Molecular Imager Gel Doc XR+. A second screening assay was carried out with restriction enzymes KpnI and HindIII in the single and double digest method following the protocols specified by New England Biolabs. Five clones were grown up in 2XYT media with kanamycin overnight in a 37°C incubator and mini-prepped the following day. Three hundred nanograms of DNA from each of the clones were used in a double and single digest with KpnI and HindIII. Fragments of the digest were run on a 1% agarose gel stained with ethidium bromide for 30 minutes at 140V. The gel was imaged using the Molecular Imager Gel Doc XR+. The sequence containing the taRNA, crRNA, multiple cloning site, and terminator was amplified from purified plasmids using pz-integration-f and pz-integration-r with Hifi Hotstart Readymix for sequencing. Sequencing was completed by Keck DNA Sequencing Facility. The alignment was analyzed using Geneious. Assembly of T7 Phage Promoter-super-folder GFP in pZA21 backbone The plasmid pZA21_T7_sfGFP was assembled from a linear fragment of sfGFP with a RBS and T7 promoter attached to the 5’ untranslated region (UTR) amplified from plasmid pZE21::sfGFP and the pZA21 backbone amplified from pZA21_tRNA_TAGG. The linear fragment of T7_RBS_sfGFP was PCR amplified from pZE21::sfGFP with primers pZE21_promT7_F and pZE21_promT7_R and Hifi Hotstart Readymix following the Kapa Biosystems protocol. The annealing temperature for the reaction was 57°C. The extension time for the reaction was 00:03:00. The reaction was treated with Dpn1 to remove remaining template DNA. Following this, the reaction mixture was run on a 1% agarose gel stained with SYBR Safe. The band was excised and gel purified following the QIAprep Gel Extraction Kit protocol. The fragment was circularized using the New England Biolabs 2X Gibson Assembly Master mix and the NEB protocol for Gibson Assembly. The resulting plasmid was dubbed pZE21::T7sfGFP. Screening for the replacement of the original PLtetO promoter was verified by sequencing. Sequencing primers for the pZE backbone pz-integration-f and pz-integration-r were used with Hifi Hotstart Readymix with the NEB protocol to amplify the multiple cloning site of the pZE21 plasmid. The amplified fragment was PCR purified using the QIAquick PCR purification kit and sent to Keck for sequencing. The sequence returned was analyzed using Geneious. The pZA21 backbone was amplified with primers T7sfGFP_pZA21_F and T7sfGFP_pZA21_R and Hifi Hotstart Readymix with the NEB protocol. The reaction was carried out with an annealing temperature of 56°C and an extension time of 00:03:00. The product was treated with Dpn1 to eliminate remaining template DNA. The reaction mixture was then run on a 1% agarose gel stained with SYBR Safe. The band was excised and gel purified following the QIAprep Gel Extraction Kit protocol. One thousand nanograms of purified DNA were then treated with a double digest using restriction enzymes AatII and BamHI-HF. The resulting fragment was PCR purified. A linear fragment of T7_sfGFP was amplified with overhangs to pZA21 containing the restriction sites AatII and BamHI-HF. T7_sfGFP was amplified from pZE21::T7sfGFP previously constructed using primers pZE21_T7sfGFP_AatII_F and pZA21_T7sfGFP_BamHI_R and Hifi Hotstart Readymix with the NEB protocol. The reaction was a two-step PCR amplification. The annealing temperature for step one was 57°C and the annealing temperature for step two was 67°C. The extension time for both steps is 00:01:10. The reaction mixture was treated with Dpn1 to eliminate remaining template DNA and run on a 1% agarose gel stained with SYBR safe. The band was excised and gel purified. One thousand nanograms of the purified NDA were treated with a double digest using the restriction enzymes AatII and BamHI-HF. The resulting fragment was PCR purified. A ligation reaction using T4 DNA ligase from NEB was conducted with the fragment of PZA21 backbone and T7sfGFP following the NEB protocol. Following the ligation, 5 μL of the reaction mixture was transformed into Mach1 cells. The colonies were picked the next day and grown up overnight. Liquid culture were started in 2XYT were started and grown up overnight. The plasmid was mini-prepped and purified. Five plasmid clones were PCR amplified using sequencing primers pZA_seq_F and pZA_seq_R in Hifi Hotstart Readymix following the NEB protocol. Primers anneal within the pZA21 backbone and amplify the multiple cloning site. The reaction was carried out with a 56°C annealing temperature and a 00:01:30 annealing time. The reaction mixture was treated with DpnI to eliminate template DNA and PCR purified. Five microliters of DNA was run on a gel to verify the presence of the fragment. The fragment was sent to Keck DNA Sequencing Facility and the sequence was analyzed with Geneious. | |||||||||||
Anti-Microbial Peptide ConstructConstruct Synthesis and Expression: Strains, Plasmids, and Reagents We hypothesize that we can develop an improved version of the current adhesives by developing a fusion protein of Mgfp-5 with Mefp-1 as the anchoring region for the anti-biofouling peptide. An integral part of developing this peptide is to co-translationally insert L-DOPA into our peptide, which has never been done before with mussel foot proteins (Figure 1). In this process of orthogonal translation, we first will get rid of the UAG stop codon and then transform the strain to synthesize tRNA and tRNA transferase that corresponds to the UAG codon and the L-DOPA non-standard amino acid to develop the genetically recoded organism (GRO). The advantage of this procedure is that we have the ability to skip the time-consuming and inefficient tyrosinase enzyme treatment step. ![]() Figure 1. Integration of L-DOPA into peptide through orthogonal translation. Protein Purification We plan to purify the protein by using the Twin Strep Tag in tandem with the Flag tag, which was included in our master construct of the anti-biofouling peptide (Figure 2). ![]() Figure 2. A diagram illustrating the components in our final construct. The Twin Strep and Flag tags are indicated. The Flag tag is perfectly cleavable by the enzyme enterokinase. The FLAG tag is made up of 8 amino acids and works well for low-abundance proteins. It is hydrophilic, so it will most likely not interfere with protein folding and function of the target protein. The Strep tag is also made up of 8 amino acids that will not disturb the protein’s functions. We chose the FLAG tag because it is perfectly cleavable. Info on LL-37 and N-terminus? The protein will be purified in a Strep-Tactin® Sepharose® column. In order to address the L-DOPA adhesive L-DOPA component, our final step is to elute with a base to reduce the amount of the anti-biofouling peptide that sticks to the column due to L-DOPA adhesion (Figure 3).
Flag Tag Sequence: Asp-Tyr-Lys-Asp-Asp-Asp-Asp-Lys ![]() Figure 3. A diagram illustrating the proposed purification method. |
|||||||||||
Methods for Assaying Coating Adhesion Properties |
|||||||||||
|