Team:Freiburg/protocols

Effector

Effector Control

Targeting

uniBAss

Modeling

Standardization

Material and Methods

Molecular Cloning

Cell Culture

Assays

Standard Protocols

Molecular Cloning

Polymerase Chain Reaction (PCR)

In order to amplify different DNA-templates, preferably from plasmids, different PCR approaches were used - with the following component amounts for 50 µl of a total volume. 31.5 µl of water, 10 µl of 5x Q5 Reaction Buffer, 4 µl of 2.5 mM dNTP solution, 1 µl of DNA template (200 ng), 1 µl of 10 µM Forward and Reverse Primer, 1 µl of DMSO and 0.5 µl of Q5 High-Fidelity DNA Polymerase. Apart from Touch-down variants and annealing temperature gradient analyses, thermocycler programs consisted of the guideline annotated below.

Assembly PCR

in case of Gibson Assemblies subsequent to fragment amplification, a reduction of fragment quantities to less than five was soon considered appropriate for more efficient Cloning. Assembly PCRs were established for halving the amounts, by using a consecutive double PCR strategy. Expect for Forward and Reverse Primers, all components of a Standard PCR were joined as mentioned above. A first PCR was done with an annealing temperature derived from the sequences of overlapping template regions. Elongation temperature was estimated by considering the fragment length of the larger DNA template (1 kBP per 30 seconds). Five cycles were performed. 2.5 µl of 10 µM Forward and Reverse Primers, both binding to the new 5‘ of both strands were subsequently added to the first PCR mix. A second PCR was performed, with an elongation temperature calculated on the basis of the assembled fragment‘s size.

Preparative Enzymatic Digest

Buffers for two or more combinatoral enzymes were selected by NEB Double Digest Finder. In order to gain high fragment concentrations in subsequent Gel Extractions, a total volume of 50 µl was mostly chosen. Typical Preparative Digests constisted of 2-3 µg vector DNA, 5 µl 10x NEB Buffer, 0.5 µl of 100x BSA, 1 µl per enzyme and were filled up to 50µl with water. Digests were commonly performed at 37 °C for two hours.

Oligo Annealing

5 µl of 100 µM both Forward and Reverse primer solutions were diluted in 80 µl of water. 10 µl of NEB Buffer No. 2 were added. Samples were heated up to 95 °C for two minutes, whereupon the heating block was switched off. After a 2-hour step of gradual cooling down to RT, the annealed oligos were stored at -20 °C.

Ligation

In order to avoid low ligation efficiencies or undesired byproduct vectors, fragment molarities and lengths were considererd as parameters for calculational schemes. Smaller fragments were mostly added excessively within between 4-fold and 8-fold molar amounts, compared to larger backbone fragments. Volume constraint often arose low Gel Extraction yields of particular fragments, so that total DNA quantities were fixed to values at around 25 ng. 5‘ dephosphorylation of single fragments was scarcely performed for reactions with high proportions of backbone religation, using Antarctic Phosphatase. Typical ligation approaches contained 2 µl 10x T4 Buffer, 1-7 µl of each fragment, 1 µl of T4 Ligase and a water fill-up to 20 µl. A 30-minute incubation step was effected at 24 °C, preceding subsequent transformation.

Gibson Assembly

Fragments with around 40 bp overlaps were obtained through PCRs with previously designed primer overhangs. According to rigidly calculated molar amounts, fragments were joined and filled up to 5 µl with of water. These 5 µl were added to 15 µl of ice-chilled Gibson-Mastermix, containing strictly defined amounts 5x ISO Buffer, T5 Exonuclease, Taq Ligase and Phusion Polymerase (Gibson et al., 2009). Samples were subsequently heated to 50 °C for one hour. Thereafter, transformation of 5 µl mix to a 25 µl aliquot of chemically compentent E. coli cells was performed.

Transformation

3-4 µl of assembled plasmids, derived from either Gibson Assemblies or classical cloning steps, were added to a 25 µl aliquot of chemically competent Top10 E. coli cells on ice. After an incubation period of 30 minutes, a 42 °C heat shock was performed for exactly 45 seconds. Subsequently, a second incubational step on ice was conducted for 2 minutes. 500 µl of previously autoclaved LB medium were added to each aliquot of transformation mix. Samples were incubated at 37 °C and 300 rpm for one hour. Transformations were finalized with plating of 500 µl of transformed E. coli solution on an Ampicillin or Chloramphenicol containing agar plate. Subsequently, plates were stored at 37 °C over night.

Colony PCR

In order to screen for positive bacterial clones after transformation experiments, Colony PCRs with available primers were done as follows. One single plate colony was picked and dissolved in 17.8 µl of water in a PCR tube, subsequently 2.5 µl of 10x Standard Taq Reaction Buffer, 1 µl of 10 µM Forward and Reverse Primer, 1 µl 2.5 mM dNTP solution and 0.125 µl Taq Polymerase were added from a previously prepared Mastermix.

Plasmid Isolation

To purify plasmid DNA from agar plates, either Roti-Prep Plasmid Mini Kit from Carl Roth or High Pure Plasmid Isolation Kit from Roche were used for Minipreps. For high yields of supercoiled, endotoxin-less DNA, Genomed‘s Jetstar Plasmid Purification MIDI Kit or Genopure plasmid MIDI Kit from Roche were used with 150 mL of transformed E. coli o/n culture. No deviances from the manufacturers‘ guidelines were incorporated by performing the isolation steps.

Isopropanol Precipitation

For an increased concentration of DNA, precipitations with Isopropanol were performed at cooled temperatures. Therefore, 1/10 of volume of 5M NaCl solution was added to the respective tube, followed by an additional 1 volume of chilled Isopropanol. Tubes were stored at -20°C for 30 minutes. A subsequent 30-minute centrifugation step at 4°C was then performed. Next, the remanent pellet was washed with 70% ethanol and centrifuged for another 15 minutes. Ethanol was finally carefully removed and the DNA resuspended in an adequate volume of deionized water.

Analytical Enzymatic Digest

In comparison with Preparative Digests, analytical controls were reduced to a significantly lower volume. Usual Master Mix aliquots contained 6 µl of water, 1 µl 10x NEB Buffer, 0.5 µl of each enzyme, and 2 µl of test DNA (~300 ng) which were thereupon added to a PCR tube. Digests were commonly performed at 37 °C for two hours.

Agarose Gel Electrophoresis

Towards PCR and enzymatic digest analyses, agarose gels were prepaired with 0,5x TAE and Agarose concentrations between 0.7 % and 0.9 % (w/v). At 65 °C, 1 µl of 10,000x GelRed was added to the Gel before a one hours polymerisation step. As a marker, 1 µl of GeneRuler 1 kb DNA ladder was loaded. Gel runs were commonly performed with voltage ranges between 80 V and 130 V for 45 minutes.

Gel Extraction

When extracting PCR bands or digested fragments from an agarose gel, the QIAquick Gel extraction Kit from Qiagen was used. Steps were performed in accord with provided user‘s manuals, including three deviances: centrifugation steps were always performed with or with less than 17,900 g, columns were rotated by 180° after washing and last, DNA-binding columns were heated to 50 °C for two minutes before the final elution step.

Cell Culture

Cell Splitting

DMEM, DPBS and Trypsin solutions were prewarmed to 37 °C. Old medium was aspirated and cells were washed with 5 ml of DPBS, which was subsequently aspirated as well. After an addition of 1 ml Trypsin, an incubation step at 37 °C was performed - until all cells showed signs of detachment. 5 ml of fresh DMEM were then added to recollect trypsinated cells from the dish. Cells were transferred to a Falcon tube and centrifuged at 900 g for 2 minutes. The DMEM-Trypsin supernatant was removed and the pellet finally resuspended in 6 ml DMEM. Seeding into a new 10 cm, 6-well or 24-well dish was performed and cells stored at 37 °C. Confluency was usually checked the day after.

Cell Seeding

For a 24-well plate, 0.5 ml cell suspension was commonly utilized per well. Accordingly, 2 ml were added to 6-wells and 10 ml per 10 cm petridish. The amount of cells depended on the respective experiment, but usually ranged from 65,000 in 24 wells to 300,000 in 6-wells and 1,800,000 per 10 cm dishes.

PEI Transfection

10 cm dish
24 µl of PEI-solution were mixed with ~ 600 µl of Opti-MEM. 8 µg of the DNA of interest was added to the solution, then the tube was immediately vortex thoroughly and had to incubate at room temperature for exactly 15 min. Finally, the solution was gently resuspended and drop-wisely spread to the cells in the dish. This was in turn swung in an 8-form.

6-well plates
7.5 µl of PEI-solution, 200 µl of Opti-MEM and 3 µg of interest DNA were used.

24-well plates
1.5 µl of PEI-solution, 50 µl of Opti-MEM and 0.5 µg of interest DNA were used.

Cell Lysis with RIPA Buffer

Cells of 24-well plates were washed with 500 µl of cooled DPBS. Then, cells were lysed in 100 µl of chilled RIPA Buffer, followed by a 10-minute incubation on ice. Next, cells were dissolved with a cell scrapper or inverted pipet tip and the developing lysate transferred to a 1.5 ml tube. Samples were vortexed thoroughly, preceding a second 10-minute incubation on ice. A 5 minute centrifugation step was done at 10,000 g. 60 µl of the supernatant were mixed with 20 µl of 4x Laemmli protein dye. Samples were heated to 95 °C for 5 minutes and afterwards either frozen at -20 °C or directly used for subsequent Western Blotting.

Assays

uniBAss

ELISA plates (Corning, Inc., cat. no. 3590, NY, New York) were coated with 100 µl streptavidin solution (20 µl/10 ml in dH20 to obtain a final concentration of 4 µg/ml) and incubated overnight at 4°C. Afterwards, plates were washed 3x with TBST (1x TBS, 0,02% Tween20) and 300 µl blocking buffer (1x TBST, 1 % BSA) were added for 1 h. After 3x washing with TBST, the biotinylated oligonucleotides (10pmol/well) were applied and incubated at RT for 1 h. Afterwards the plates were washed 3x with TBST. To obtain the cell lysate with the Cas9 protein, the transfected HEK 293T cells (250.000 cells/ml) were resuspended in 250 µl dilution buffer (10 mM Tris, 1 % BSA, 10 mM MgCl2, 10 mM NaCl) containing EDTA free Protease inhibitor per 125.000 cells/ml and sonified for 10 min. To remove the cell fractions the lysate was centrifuged for 5 min at 500g. Afterwards 80 µl or 100 µl of the diluted cell lysate were transferred to the ELISA plates. After 1 h incubation at RT the plates were washed 3x with TBST and 100 µl anti-HA antibody solution (1000x diluted in blocking buffer) was applied to each well and incubated for 1 h. After 3x washing with TBST, 100 µl anti-mouse HRP antibody (4000x diluted in blocking buffer) were added. After 1 h incubation, plates were washed 3x with TBST, probed with 100 µl ELISA ABTS substrate and the absorbance was measured at 405 nm. For the positive controls, wells were coated with 100 µl FM protein (1.0 µg/ml) and directly with the sonificated cell lysate in the dilution buffer.

SDS-PAGE & Western Blot

For efficient detection of proteins in our studies, especially dCas9 and it‘s targets, cells were transfected and after 48 h cell lysis followed. SDS-Gels (10 % SDS) were performed in Invitrogen-cassettes or Biorad-systems. Therefore, resolving- and stacking-gels were poured as listed in the according table.
The bags were loaded with 20 µl sample or 10 µl marker (cell lysates were boiled at 95 °C in 1x Loading Buffer for 5 minutes before). Runs were performed at 80 volt until the samples had reached the resoltution gel. Then, the voltage was increased to 120 volt. Gels run until the blue frontline had passed the gel completely.
Afterwards, blotting in a wet tank followed. Therefore, PVDF-membranes were activated for 5 minutes in methanole. Then, they were passed to transfer-buffer just as the Whatman-Paper. The blotting sandwiches were prepared as follows, started from the bottom:

Microscopy

Seeding
For microscopy experiments, 50,000 cells were seeded in 0.5 ml DMEM on sterile cover slips in 24-well plates.

Fixation
Cells were treated with 200 μl of 4 % PFA solution and stored at 4°C for 30 minutes. In order to avoid any bleaching, cells were covered with aluminum foil.

DAPI-staining and mounting
DAPI was used for visualizing the nucleus. Therefore, cells were dipped into a DAPI solution (1:10,000) for 5 seconds - right before mounting on microscope slides. Next, the cells were washed for 5 seconds in distilled water, had to be dabbed of with a tissue and were then placed upside down on a drop (8.5 μl) of mowiol. The cover slips stayed for an overnight drying at room temperature.

SEAP Assay

80 µl of cell supernatant was transferred from a 24-well plate into one 96-well plate (flat bottom), followed by a heat incubation at 65 °C for 30 min. Centrifugation was done for 1 min at 1250 g. 100 µl of 2x SEAP buffer (20 mM homoarginine, 1 mM MgCl₂, 21 %(v/v) diethanolamine, pH 9.8) were added to each well. Addition of 20 µl pNPP (120 mM para-nitrophenyl phosphate in H₂O) and bubbles carefully removed. Immediately after this, the 96-well plate was placed into a plate reader. Spectroscopic measurement was taken every minute for 120 times (2h) at a wavelenght 405 nm.

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