(r3) Barrick Lab :: ProtocolsFluorescentProteinEvolutionaryStability

---+ Evolutionary Stability of Fluorescent Protein Expression

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This procedure is to monitor the decay of a genetic device that outputs GFP fluorescence as a microbe replicates, it accumulates mutations that lead to a loss in fluorescent signal, and these mutant cells outcompete cells with fully functioning copies of the device.

---++ Procedure: Growth

   1 Plate the ancestral strain to isolate single colonies
      * %ICON{warning}% It is very important to start from *brightly fluorescent* single colonies so that any existing genetic variation in a stock culture is purged (which is very common for devices that lose function rapidly). Only in this case are the observed decay curves and breakage mutations evolutionarily independent!
   1 Pick *entire* single colonies from these plates and resuspend each one in a 10 mL culture in a 50 mL flask. These are your replicate cultures.
      * It is important to get the entire colony, because then one can figure out exactly how many cell divisions have taken place from the single cell that initiated the colony.
   1 Each growth cycle (usually 24 h) transfer 100 µL of the overnight culture and into 10 mL of fresh media and either store the culture or immediately take a measurement (methods for this explained below).
      * This 1000-fold dilution equals 10 generations of binary cell division.

---++ Procedure: Measurement

---+++ Measurement by Plating<br>
There are essentially two ways to do this by plating, either by <b>spreading</b> an inoculum across the whole plate or by <b>spotting</b> inocula as serial dilutions. Both involve counting colonies and the readout is the ratio of fluorescent colonies divided by the number of total colonies. Though spreading consumes a significantly higher number of plates, it also allows detection of smaller changes in fluorescence, as typically 30-300 colonies can be counted on such plates while only about 6-60 colonies can be counted during spotting. <p>

<b>Spreading</b><br>
1) Estimate the cfu/ml of the overnight culture via OD600 measurement. There is a web calculator available [[http://www.genomics.agilent.com/biocalculators/calcODBacterial.jsp][here]]. Note that to measure OD600 accurately you may have to dilute your culture as this is most accurate in the range of OD600 in the range of 0.1 to 1.0. <br>
2) After estimation, dilute the culture in saline by taking 100 &#956;L, adding it to 10 mL of saline, vortexing, and repeating the dilution process as needed. The ultimate goal is to dilute the cfu/ml to a point where spreading 50-100 &#956;L would yield about 30-300 colonies.<br>
3) Add sterile glass beads to LB agar plates with antibiotic, then place the appropriate amount of the diluted culture on the beads.<br>
4) Shake the plates back and forth to ensure that the inoculum is spread uniformly across the surface of the agar.<br>
5) Incubate at 37°C for 24 h.<br>
6) Count the total number of colonies overall. If desired, you may use a colony-counting software such as [[http://opencfu.sourceforge.net/][OpenCFU]], but it may be easier to simply do it by hand. If you do decide to use such software, please double-check the automated counts to eliminate any false positives and false negatives.<br>
7) Count the total number of nonfluorescent colonies using blue light. Remember to place the orange filter on top and, if desired, wear the orange safety glasses.<br>
8) Now, to calculate the ratio, subtract the number of nonfluorescent colonies from the number of total colonies. This will yield the number of fluorescent colonies. Then divide by the total number of colonies.<br>
9) Plot the ratio as a function of time over several days. The expected result is a significant drop in this ratio over the course of a few days representing the decay of the genetic device.<br><p>

<b>Spotting</b><br>
Note: This protocol was adapted from [[http://www.sciencedirect.com/science/article/pii/S2215017X15000454][Thomas, Sekhar, Upreti, Mujawar, & Pasha (2015)]]. <br>A convenient flowchart of the protocol (though altered) can be found [[http://www.sciencedirect.com/science?_ob=MiamiCaptionURL&_method=retrieve&_eid=1-s2.0-S2215017X15000454&_image=1-s2.0-S2215017X15000454-gr1.jpg&_cid=306229&_explode=defaultEXP_LIST&_idxType=defaultREF_WORK_INDEX_TYPE&_alpha=defaultALPHA&_ba=&_rdoc=1&_fmt=FULL&_issn=2215017X&_pii=S2215017X15000454&md5=6431285061dfe74eaa41baaae2b73ba5][here]]. <br>
1) It is no longer necessary to estimate the cfu/ml of the overnight culture, as each plate is capable of enumerating colonies over a range of 6 orders of magnitude as opposed to the above method. Instead of diluting the overnight culture in 10 ml of saline, set up a serial dilution series of sterile microfuge tubes each containing 900 &#956;l of saline. Each tube represents a tenfold dilution (and thus should be labeled -1, -2, -3, etc.) and I recommend diluting out to 10^-7. Contrary to what the paper advises, I do not recommend diluting the overnight culture to an OD600 of 0.1; it is unnecessary. <br>
2) Place 100 &#956;l of the overnight culture into the microfuge tube representing 10^-1 and vortex. Please note that taking 100 &#956;l from this would actually be a 10^-2 dilution (the overnight culture is first diluted tenfold after being added to the saline, then you only take 1/10th of the dilution to plate). This will be accounted for in the final formula to back calculate cfu/ml (if desired). <br>
3) Label your LB agar plates with antibiotic by dividing most of the plate into 6 sections. Each section of the plate will be used to spot a different dilution of the same culture. Thus, the six sections may be labeled -2, -3, -4, -5, -6, and -7, for example.<br>
4) Spot 10 &#956;l of each dilution in triplicate onto the corresponding section of the plate. The paper recommends 20 ul but that seems to cause the spots to run into one another and it also takes longer to dry, increasing the chance for contamination.<br>
5) Dry out the plate in the 30°C or 37°C incubator with the lid slightly off to allow moisture to evaporate. This part can take 15-20 mins depending on temperature and how moist the agar itself is.<br>
6) Place the lid back on fully and incubate at 37°C for 24 h. The resulting plate should look like the [[http://www.sciencedirect.com/science?_ob=MiamiCaptionURL&_method=retrieve&_eid=1-s2.0-S2215017X15000454&_image=1-s2.0-S2215017X15000454-gr5.jpg&_cid=306229&_explode=defaultEXP_LIST&_idxType=defaultREF_WORK_INDEX_TYPE&_alpha=defaultALPHA&_ba=&_rdoc=1&_fmt=FULL&_issn=2215017X&_pii=S2215017X15000454&md5=9f3ddd1a809fe90f9894f4636a0a1440][example plate on the left here]].<br>
7) Calculate the ratio of fluorescent to nonfluorescent colonies. <br>
8) Plot the ratio as a function of time over several days. <br><p>

Troubleshooting: <br>
a) The incubation period is around 24 h because colonies that are too small may not appear fluorescent (even if the genetic device is intact) and thus act as false negatives. However, growth rates can vary and you should check on colony growth before 24 h if colonies have grown too large and start to overlap.<br>
b) Fluorescent colonies can stay fluorescent for a couple of weeks in the fridge, so feel free to store them at 4°C and count them later if desired.<br>
c) If there is large variation between technical replicates, ensure you are vortexing for a few seconds after every dilution step.<br>
d) While drying the inocula during the spotting method, even though the plate is somewhat open and exposed for a period of time, it is unlikely that you will get any contamination. If this turns out to be a problem, you may also dry your plates in a biosafety cabinet which will take longer due to lower temperature but reduce the risk of contamination.<br>

---+++ Measurement by Microplate Reader

1) Plan out which wells will contain what sample. You can print out one of the 96 well plate templates available [[http://www.cellsignet.com/media/plates/96.jpg][online]]. Generally, each condition should be done in quadruplicate (or triplicate depending on space concerns). <br>
2) After vortexing your sample, aliquot 100&#956;L at a time into each well. You should use the appropriate type of plate for your application: black walled, clear bottom for fluorescence (white walled, clear bottom is generally for luminescence and completely clear is generally for other applications, like measuring OD600). <br>
3) Ensure that you have adequate controls. At the very least, have a nonfluorescent negative control of E. coli in the same media grown under the same conditions, either empty vector or isolated from a colony that had lost its fluorescence. <br>
4) Turn on the plate reader - there is a power button in the back next to the power cord - and then turn on the Magellan software on the computer next to it. Not doing it in this order may cause the software to fail to recognize the machine. <br>
5) Select the option that says "raw data" and eventually you will find yourself at a configuration screen. <br>
6) First, select the brand and type of your plate next to the "Plate definition" dropdown menu. <br>
7) Second, using ctrl click, select the wells you want to measure. <br>
8) Third, you must add a measurement step. Double click "Fluorescence Intensity." Set your Excitation and Emission values to integers appropriate for your fluorophore and change Gain to "Optimal". You can also manually set gain by testing different values: generally, a higher gain detects smaller amounts of fluorescence; if you get overflow reads in several wells, you should set the gain lower. <br>
9) Fourth, perform the measurements and save your data. Unfortunately, there is no Excel installed on that computer, so "Copy to Excel" is not a possibility at this point. Data is saved by default as ".wsp" files. (Still looking for a workaround - there is also a "Copy as ASCII" option that I haven't tested yet). <br>
10) Finally, after performing this over a number of days, calculate how RFU changes as a function of time. <p>

Troubleshooting: <br>
a) If you are not sure what the excitation/emission values for your fluorophore are, here is a handy reference courtesy of Simon: [[https://slack-files.com/files-pri-safe/T04QHM990-F0Q59MJMD/filter_combinations_fps_spectra.pdf?c=1457108292-b10ad8f9e80d418c5d5e0ca0a9b5d994bb51795d][Spectra of Common Fluorophores]]. <br>
b) You can BLAST the gene sequence of your fluorophore to check which it matches (most likely a variant of EGFP). If you are still not sure or getting bizarre results, you may want to do a "Fluorescence Intensity Scan" where you set the plate reader to test numerous wavelengths of excitation in a certain range and then look at the spectra to see where the peaks (highest RFUs) are, in terms of wavelength. <br>

---+++ Measurement by Flow Cytometry

*Note*
   * _E. coli_ fluorescence seems to be relatively stable for up to ~7 days at 4°C in these measurements.

   1 Aliquot 100uL of cells into 1.5 mL tubes, add 1 µL of [[https://www.thermofisher.com/order/catalog/product/T13320][FM 4-64 membrane dye]]
   1 Incubate cells + dye for 10 min, shaking at 37°C.
   1 Spin cells down for 5 minutes at 3000 rpm.
   1 Remove media and resuspend with an equal volume of saline or PBS.
   1 Proceed to using Flow Cytometry to count.
   1 After fluorescent has been assayed, plot the %FP over the number of days 

---+++ Measurement by Next-Gen Sequencing

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---++ Expected Results

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Barrick Lab > ProtocolList > ProtocolsFluorescentProteinEvolutionaryStability
Contributors to this topic
JeffreyBarrick, LucyLeblanc, DennisMishler, DaciaLeon
Topic revision: r3 - 2016-03-21 - 17:22:26 - Main.LucyLeblanc