The Nav channel bench series: Plasmid preparation☆

Graphical abstract


Method details
Step 1: transformation Materials high quality starter Na v plasmid DNA Max Efficiency 1 Stbl2 competent cells (Life Technologies) LB plates (with antibiotic at half-standard concentration) SOC or comparable outgrowth medium [8] dedicated 30 8C incubator and shaker Note: This list includes only non-standard items. Generic components such as water baths and baffled flasks are assumed to be available.
Analyses of Na v channel function begin with the construction or purchase of an expression vector (e.g., pCMV-Scrip, pCI-neo) containing a Na v channel's coding sequence. Alternative splicing is common among Na v channels, creating different proteins from the same gene with distinct spatial and temporal expression patterns [9][10][11][12]. Careful planning is therefore necessary to determine exactly which isoform and coding sequence are needed to address the questions of interest. With approximately 6 kb in length, Na v channel coding sequences are long, making final insert-vector plasmid construct sizes in excess of 11 kb common. Regardless of its origin, be it a gift from a colleague or purchase from a commercial supplier, comprehensive sequence information ought to be part of the plasmid construct transaction. This will allow the end user to be fully informed when it comes to restriction analysis of the plasmid, which should always be the first step upon the DNA's arrival. Simple electrophoresis of small aliquot of plasmid DNA digested with a reliable enzyme that produces a known banding pattern will show whether the plasmid is correct or not. This may seem trivial, but cases where providers less experienced with Na v channel handling send corrupted DNA are not uncommon. If above mentioned restriction digest does not deliver the expected results (be selective here; minimal changes can be telltale signs of problems), digest with an alternative enzyme to confirm.
Once the restriction enzyme digestions delivered the appropriate restriction fingerprint, bacterial transformation can begin. We have had good success with chemical transformation as described below, but electroporation of suitable bacterial strains may be a viable alternative. Contrary to standard transformations, competent cell choice is critical when comes to Na v channels. Among the cell lines known to be susceptible to produce problems are JM101, DH5a, One Shot Top10 1 , to name but a few. Transforming these cells according to the manufacturer's instructions has a high chance of producing a negative outcome, although in select cases success appears to be possible (JM109, unpublished data). In our hands, by far the most reliable and successful is the Stbl2 bacterial strain, whose genotype favors cloning of problematic plasmid DNA. Although somewhat costly, it is possible to refreeze them at À80 8C in 25-ml ready-to-use aliquots using immediate immersion in ethanol/dry ice without losing too much efficiency, should a more economical solution be necessary.
Once the transformation is completed, the bacteria are propagated on LB plates with an appropriate antibiotic, at approximately half-standard concentration (e.g., 50 vs. 100 mg/ml ampicillin), at 27-30 8C. Because this temperature is lower than the 37 8C incubation used in standard procedures, using a lower concentration of antibiotic will allow faster bacterial growth without compromising the selection of resistant clones. It is very important at this point to emphasize the use of a dedicated and appropriately labeled 30 8C incubator. Any temperature elevation of Stbl2 cells above 30 8C will inevitably corrupt Na v channel DNA through host-mediated mutation (personal observation). At this temperature, the growth of bacteria harboring Na v channel DNA is very slow, and incubations of 3-5 days are often necessary. At no time during this period can the temperature exceed 30 8C. Appropriate signage ought to be attached to the incubators to ward off secondary users who may briefly change the incubator temperature to the standard 37 8C unbeknownst to the Na v channel researcher.
Procedure ice-chill 2 ml (20 ng) of plasmid DNA in the bottom of a Falcon tube thaw a 25-ml aliquot of Stbl2 cells on ice for 5 min, then pipette over the chilled DNA and mix with gentle pipette tip agitation incubate on ice for 25 min, then heat shock in a 42 8C water bath for 40 s and immediately return to ice for 2 min add 400 ml of room-temperature SOC and shake in a pre-warmed incubator at 30 8C for 90 min plate 50 and 250 ml of the cells on two separate, pre-warmed LB plates with antibiotic at halfstandard concentration following a 10-min right-side up absorption at room temperature, place the plates upside-down in the dedicated 30 8C incubator allow to incubate for several days until two distinct populations of colonies have emerged: large fast-growers and tiny slow-growers Step 2: bacterial growth Materials dedicated 30 8C incubator/shaker 1 l LB broth (selective antibiotic at half-standard concentration) Note: As in Step 1, this list includes only non-standard items. Also required are commercial plasmid prep kits (mini as well as maxi), gel electrophoresis instrumentation, and associated consumables.
As mentioned earlier, the success of the transformation will not be known for several days. Although colonies might be visible the morning after the first overnight incubation, these fast growing colonies very likely carry corrupted plasmid DNA and should be avoided. In the cases that we have examined, the extent of the associated genetic alterations in fast growing colonies varied greatly, ranging from point mutations to large-scale rearrangements. The best approach is to wait for 2-3 days before the plates are scanned for colony growth, in which time, a second, slow-growing population of exceedingly small colonies will become discernible. To make colony spiking easier, incubation at 30 8C or room temperature may continue for up to 5 days. Care should be taken when ampicillin is used as the selective antibiotic. Rapidly growing resistant colonies will secrete beta-lactamase that can allow growth of non-resistant cells, which will appear as small, slowly-growing satellites surrounding fastgrowing colonies. Bias toward slowly-growing, well-separated colonies helps avoid this issue. An alternative approach is to use an antibiotic such as for tetracycline for which resistance is only effective in the cells that express the resistant gene.
We recommend spiking 10-20 colonies to generate standard LB mini-cultures; the concentration of the selective antibiotic should be identical to that of the previously used plate. Shaking proceeds at standard speeds in standard round-bottom tubes. Maintenance of the 30 8C rule is crucial, which translates into 2-3 days of growth to reach the desired density, although shorter incubation times have been observed. We have experimented with richer media such as terrific broth, but the results were mixed. Terrific broth does accelerate bacterial growth, but it is also more prone to overgrow, which creates downstream problems in plasmid isolation if the growth is not stopped in time.
Once the cultures have reached the appropriate turbidity, they are processed with any standard mini plasmid prep kit since no one commercial kit is advantageous over another. However, it is important to use the maximal amount of cell material allowable per manufacturer's instructions; we commonly process 1.5 ml of culture. The eluted DNA is subjected to the same restriction analysis employed upon arrival of the original DNA. For this digest, simple mixing of the eluate with restriction buffer and enzyme (without addition of water) should yield the best results, as the DNA concentration is likely very low. Alternatively, a smaller elution volume may be used to achieve more concentrated DNA samples.
Provided the mini culture analysis generated the expected restriction pattern, a maxi culture can be started. We commonly increase the manufacturer's recommended culture volume by a factor of 2 or 3 for the culture setup. In other words, if a 200-ml culture is suggested, we usually grow three baffled flasks of 200 ml LB with the aforementioned half-standard antibiotic concentration. Inoculation is done at 1:1000 by adding 200 ml of the original mini-culture (kept at 4 8C) per flask. Best practice is to process the mini-preps and inoculate the maxi-cultures on the same day.
Contrary to all previous incubations, the maxi cultures, while also grown at 30 8C, usually grow quicker and reach sufficient turbidity after only an overnight shake. One can now process the cultures according to the manufacturer's recommendations. We do recommend individual processing of each maxi culture to avoid clogging of the filtration columns after alkaline lysis. However, the DNA from all three setups can be combined in the final step by serial passage of the eluate from one column to the next. Alternatively, one could simply combine the three eluates and reduce their volume in a speedvac, granted that water was used in the elution step.
Procedure following several days of growth, inspect the LB plates and identify suitable slow-growing, small colonies using autoclaved toothpicks, inoculate several 3-ml LB mini cultures (half-standard antibiotic concentration) shake at 30 8C for 2-3 days until the cultures turn turbid process 1.5 ml of mini cultures according to the instructions of the available mini prep kit using water in the final elution step; store the remainder of the mini culture at 4 8C using only restriction buffer, enzyme, and eluate, set up 20-ml digests and separate with standard gel electrophoresis identify a setup with the expected restriction fingerprint and 1:1000 inoculate two to three 200-ml maxi cultures (LB, half-standard antibiotic concentration) with 200 ml of mini culture shake at 30 8C over night process each 200-ml culture separately according to the maxi prep kit manufacturer instructions; only the final TE buffer elution step is customized: combine the DNA yield by sending the eluate from the first silica column through the second (and the third, if three maxi cultures were processed); intermittent volume adjustment of the eluate with additional TE buffer may be necessary Step 3: DNA sequencing Once the maxi prep DNA has been obtained, standard spectrophotometric analysis will help determine the DNA concentration, and restriction fingerprinting as described earlier will confirm the isolated DNA's identity. Despite all optimization efforts, the DNA yield may be low, which may interfere with DNA sequencing. Service facilities frequently request plasmid concentrations in excess of 1 mg/ml for double-stranded DNA larger than 10 kb. Therefore, the initial elution volume can be kept small to achieve higher concentration of working DNA, which can then be diluted to the desired level if needed. Moreover, it is our experience that close communications with the sequencing facility staff can also help address these issues. With additional care and informed personnel, we have not had any problems sequencing our Na v channel plasmids, even at concentrations as low as 100 ng/ml.
Full-length sequencing encompassing the entire Na v coding region is essential. With today's DNA sequencing technology, primer walking with 600-800 bp intervals ought to generate reliable results. We additionally process our chromatograph data using Nucleics' online PeakTrace application, which aids in clearing base-calling ambiguities. All sequencing data is routinely aligned to our reference sequence (preferably an NM RefSeq or LRG record -hyperlinks provided in Additional information section) where an experienced reviewer visually confirms all base calls. Questionable areas ought to be re-sequenced and, if necessary, primed in both directions. We provide a list of sequencing primers in the online material of this article. Once the Na v channel DNA has been certified in this fashion, it can be used for transfection and/or mutagenesis for downstream analysis of the channel function.

Additional information
Background Voltage-gated sodium (Na v ) channels control excitation in brain, heart, and muscle. Deviations from their tightly defined functional characteristics, for example through genetic alterations, lead to heritable pathology that reflects the spatial and temporal expression pattern of the affected Na v channel gene ( [1][2][3][4][5][6][7], reviewed in [13]). Pharmacological control of the clinical symptoms in these socalled Na v channelopathies (e.g., epilepsy, cardiac arrhythmia, muscle cramps, pain) is often hampered by treatment-emergent adverse effects due to structural and functional similarities among the Na v channels that make isoform-specific targeting difficult. Improved intervention may be possible with patient-tailored therapy, where the drug action counters the defect of the faulty Na v isoform without affecting other Na v channel function. Such drug development efforts are challenged by the unique requirements that come with recombinant DNA work involving Na v channel coding sequences, because Na v channels are notoriously difficult subjects when it comes to bacterial plasmid amplification, mutagenesis, and stable cell line development. The basis for this behavior is unknown, and no study researching the same has been published. One may speculate that the combination of exceptionally large coding sequences with internal homologous repeats is involved. There is evidence that Na v channel DNA in itself is toxic for the bacterial host, since random mutation events are not limited to full-length Na v channel coding sequences, but they also occur during bacterial propagation involving Na v channel DNA fragments (personal observation).