Week 1: June 6 - June 11

In the first week we began constructing basic reporter DNA constructs that have various combinations of promoters and genes. The mix-and-matching of promoters and genes was done using the LR reaction following the Gateway protocol. Our promoters included TRE, minCMV, Hef1a, Hefl1a-LacO, and our genes included eYFP, mKate, and eBFP2. Transformed and inoculated colonies from the LR reactions and performed restriction digests. Approximately half of the LR reactions were successful and became DNA parts that we could use later on.

June 7, 2011

LR Reactions
Utilizing protocol here: LR Protocol

Transformation

Miniprep

Restriction Digests

Gels

June 10, 2011

Restriction Gels

Comments:

pEXPR_2-3_Tre:LexAVP16 and pEXPR_3-4_minCMV-7xMnt1:eYFP are being entirely redone.

pEXPR_2-3_Tre:LexAVP16 (post-miniprep) was lost. pEXPR_3-4_minCMV-7xMnt1:eYFP LR was unsuccessful (no bacteria grew).

LR and transformation will be done on Saturday. Miniprep and restriction mapping will be done on Sunday

June 11, 2011

Set of LRs from 6/9 (GR, JC, and SR) cell counts taken; inoculated by GR/JC. 3 cells taken per plate.

Week 2: June 12 - June 18

In the second week we attempted midipreps instead of minipreps of our available cell stocks. Midipreps were unsuccessful, likely due to centrifuge limitations. LR reactions to generate more usable promoter-gene pair parts continued, expanding to include the CI434-VP16, LexA-VP16, and Mnt-VP16 genes, whose expressed proteins activate the appropriate corresponding minCMV promoters. Most of the LRs done were not successful, reason unknown at this time.

Week 3: June 20 - June 24

In the third week we continued expanding our library of usable DNA parts by creating more combinations of genes and promoters using the LR reaction.

Week 4: June 27 - July 1

In the fourth week we implemented a color-coded box system in our -20 freezer to accommodate for the growing need of organization of the growing number of DNA parts. We began learning and using the Gibson reaction to create the gene part AVPR2-TEVs-GV16, which is expressed to produce a vasopressin receptor bound to Gal4-VP16 by a TEV sequence that can be recognized by the TEV Protease. Gibson reaction results were not great, and it appeared that our AVPR2 DNA was not of sufficient quality, so we re-PCRed the AVPR2 DNA segment.

Week 5: July 4 - July 10

We began looking into using the Goldengate assembly method, but two gene elements contained a cut site that needed to be mutated out. We performed Site-Directed Mutagenesis using the Lightning Kit in the hopes of mutating out the cut site, but results were not successful due to mishandling during the protocol, so the procedure was set to be repeated. Gibson assembly of AVPR2-TEVs-GV16 continues as we re-PCRed the AVPR2 DNA segment and re-run the entire Gibson protocol, picking 20 colonies in a determined attempt to obtain a successful result.

Week 6: July 11 - July 17

In the sixth week we continued re-attemping previous failures using modified protocols or higher quality DNA in hopes of obtaining successful reactions. We also began looking at Cadherins and the possibility of using them as a clumping mechanism for mammalian cells. In order to visualize Cadherins, we needed some sort of fluorescent color, so construction of NCadherin-EGFP (NCadherin is one of many types of cadherin) began. DNA for NCad-EGFP was ordered, but needed to be in a format such that we could LR react it with the different promoters we have. This is done by attaching attB sites to flank the NCad-EGFP gene and then performing the BP reaction, which generates LR reaction-compatible parts. PCR of the attB sites was successful. By this week we have also begun work with mammalian cell cultures. To explore the limitless possibilities of synthetic biology, a few of us took it upon themselves to look into other interesting gene components, such as the Caspase gene and the FF4 tag.

Week 7: July 18 - July 24

Part of the team worked on creating protocols for a robot liquid handler to run the usual lab reactions that we run. We are hoping that the robot can replace us and do our liquid-related lab work for us. Various dry test runs were done. We transfected various DNA parts that we have into Hek293 cells, and results show that most of our DNA works. We investigated the TRE-rtTA3 system as well as the UAS-Gal4 system. Both seemed to be functional.

Week 8: July 25 - July 31

This week we underwent a momentous drive to create more LRs. A large list of promoter-gene pairs was conceived of and we began to run through LR reactions in somewhat of a factory manner. This occupied much of our time. We also received and prepared DNA parts from Elowitz's group in Caltech. We also got trained on using the FACS machine and began to get quantitative data on our transfections.

Week 9: August 1 - August 7

In the ninth week we did a lot of internal re-organization to increase our overall efficiency in work. This involved re-organizing an internal wiki that we use for management of our available DNA as well as a log of transfections needed to be done. Lots of samples were FACS-ed, generating lots of results that we can make graphs out of. Many of our parts were successfully characterized.

Week 10: August 8 - August 14

Computer simulations of the Notch-Delta interactions were presented in our group this week, and we became convinced of the possibility of creating self-patterning mammalian cells. On the DNA side of things, we are trying to create more and more DNA using miniprep, because midipreps have for some reason not been successful for us or the 2010 iGEM team. On the transfection side, a lot of new DNA parts were transfected, observed under the microscope, and FACS-ed to quantify their effect/behavior. h3. August 14 Charles - Miniprepped propagations of various things, good CP LRs, as well as re-inoculations of poor CP LRs. Nanodrops were all over hte place. Some of the re-inoculated CP LRs reached 500 ng/uL, which was weird. &nbsp; Divya - Ran FACS on 50 samples for Tyler and Ken. Also, I now have Koch access\! Woohoo\!\!\! Kenneth - Prepped FACS samples. Moved frozen cells to ln2 Grant - Today and yesterday did sequencing of Tango and other plasmids as well as propagations of a handful of failed plasmids / spinning down of cells for Charles' miniprep. h3. August 13 Kenneth - Added delta to cells. Co-cultured AVPR and pDisplay Vasopressin cells. Froze down and passed the Elowitz CHO cell lines and put in \-80. Also passed wells and flasks. h3. August 12 Kenneth - Transfected cells for AVPR2 experiment as well as another free delta induction experiment, this time with const. color gating. Charles - Attended Ken's orientation session and did 1 transfection just to try things out. Also obtained my new culture of cells. Cell stocked CP LR 4,5,6,7,8,11,12, of which 4,5, and 7 are tentative (repeat submitted). Re-inoculated failed CP LR's 1,2,3,9,10 with a different colony. Also propagated a whole bunch of plasmids, including the successful and tentatively successful CP LR's. Hopefully the color palette will be complete by Tuesday. &nbsp; Jon - Tissue culture orientation & inoculated SDM transformations from yesterday. Colony counts around 20 for TEV and 3 for GV16. h3. August 11 Jon - Redid GV16 and TEV SDM with new primers; transformed, hopefully they work this time. Clara: Miniprepped and nanodropped 12 LRs from Aug 9. Hef1a: Delta-mCherry has esp. low concentration. To see conc. of other samples, refer to 8/11 [iGEM2011:Clara's Notebook] Tyler: Prepared cells for transfection tomorrow. Plan on doing the following experiments: NCAD phenotype, TRE:LacI and TRE:LacI-Krab with proper gating, Hef1A:GV16 with proper gating, DRD2 repeat, and possible CCL5 experiment. Did FACS on&nbsp;[iGEM2011:Confluency Experiment]&nbsp;which shows best starting value around 1.5*10^5 cells/mL starting concentration. FACS machine showed around 40% efficiency. Matlab shows around 30%. In either case, we should start transfections with cells less confluent than we have been. TRE:LacI-Krab experiment seems to have worked, but there is only about 2x repression (see bottom of&nbsp;[Tri-Color Experiment v2|iGEM2011:Tri-Color Experiment v2]). Also put up FACS from AmCyan which is more green than blue. Michelle: Prepped Clara's 12 minipreps for sequencing. Worked on Circuit Diagrams and write ups for the public wiki. Charles: 42 FACS in less than 1 hour. Very fast because Ken's samples were concentrated. h3. August 10 Tyler: I updated the wiki (first (per usual(winning))). Prepared for FACS. Transfected Confluency Experiment ([iGEM2011:Confluency Experiment]). Will FACS tomorrow. Still need FACS data from Divya for Tre:LacI-Krab experiment and some AmCyan colors. Today Jenny FACSed some DRD2 (apparently a failure from pictures) and some Delta-Notch stuff (also a failure). Need to look at the FACS, which apparently disappeared today? so hopefully we can find that tomorrow as well. Will try DRD2 (+100 uM dopamine) again later in the week with possibly more dopamine.&nbsp; Charles: Completed Tyler's Hef1a_GV16 page with pretty FACS images. Watched Jenny do FACS at Koch. Some problems with either no cells in sample or visibly clumped cells. Introducing a new page...&nbsp;[iGEM2011:Color Palette] Michelle: Inoculated Clara's LRs. Ready to miniprep and send for sequencing tomorrow. Grant: Miniprepped, restriction mapped, and sequenced the minCMV promoters and a few other genes/promoters. Started LR reactions for a few more Tango parts and the Ephrin parts. Shockingly did nothing else. h3. August 9 Kenneth: Worked on MATLAB stuff more. Treated TRE:mKate and TRE:eBFP2 experiments with dox. Transfected for pDisplay immunofluoresence experiment again. Thawed out Elowitz cell lines. Froze down large numbers of HEK and CHO cells. Passed cells into 60 mm plates for N-cad knockdown experiment. FACS data analysis. Prepared dopamine aliquots and supplies for future experiments. Grant: Removed propagations of various gene/promoter entry vectors and inoculated a single colony from each. Did alignments of sequencing data for samples sent out yesterday. One LR reaction failed unexpectedly, but the other failures involving minCMV promoters appear to have occurred due to contamination from a Hef1a variant promoter based on a BLAST of the sequencing results. (READ: The "minCMV" promoter DNA is not actually minCMV promoter DNA\- at least this is the case for the tubes without stickers.) All parts currently being used for experiments are verified. On track for \~15-20 new LR reactions for Wednesday afternoon. Clara: 12 LR reactions, left at room temperature @ 12:30pm~. Refer to [iGEM2011:Clara's Notebook]&nbsp;for details. Charles: Transformed Clara's LR reactions. Had to leave during the middle of the day to go to the Student Services Office. Watched Mariola's presentation. Working on a new page. Jenny: TriColor FACS are now up on their appropriate pages. Rest are temporarily on my notebook. Tyler - Updated the wiki. Need to redo all of the FACS data tomorrow that Jenny did today because the red and blue colors are switched. Mariola's program works so I will use that. Tomorrow I will do transfections of a consistuitive color into wells with different confluencies that I set up today. I added Dox and Dopamine to wells today that we will FACS tomorrow.&nbsp; Michelle/Divya: Miniprepped and nanodropped 12 samples. Prepped other samples for sequencing. h3. August 8 Kenneth: planned out and did transfections for TRE eBFP2, TRE:mKate and AVPR2 validation experiments. Also threw in a co-culture of Notch/Delta cells, only with UAS:eYFP instead of UAS:citrine from Elowitz. Not expecting anything from that, but just covering all bases. Treated pDisplay-vasopressin-myc cells with anti-myc FITC Ab and prepared slide. Results suggestive. Cells were too confluent at time of fixation, many were washed off and the remaining look bad. Probably from my bootleg formaldehyde solution as well. However, remaining cells were green on the surface as well as red from delta-mcherry, while controls are not green. Seems to suggest it is being displayed... Grant: Miniprepped the EPHB2, EFNB1, and CXCR1-TEVs-GV16 pENTR vectors assembled previously. Set up fourteen sequencing reactions of multiple Tango plasmids and a few reporter expression vectors designed to test the minCMV promoters, as well as the three ENTR vectors miniprepped. Pending affirmative sequencing results, LR reactions will begin. Because we need a number of promoters propagated and it would be nice to do LRs with the Rheoswitch system (and possibly the new Notch constructs) concurrently, I will probably wait to begin these. Cleaned the lab before the start of the work day, like a boss, or perhaps a janitor. Started propagations of a few promoters and genes that we had < 1 uL of DNA left of (and no cell stock), because if you want something done... Tyler: Transfections Charles: Propagated DNA we are low on. Looks like Grant also did this. So we should be stocked. And miscellanea. Mariola: Aliquoted and Transfected UAS:EGFP and TRE:eyfp-4xFF4 experiments. Dox ladder of each. Writing 8pg REU paper and presentation. DMC: Prepped and submitted several samples for sequencing. See Divya's Personal Notebook. Brought presents from Weiss Lab (SalI-HF, 10uL tips, 1000uL tips).&nbsp; {cloak}

Week 11: August 15 - August 21

In our experimental attempt to characterize the Notch-Delta interaction, we used co-culture of CHO and Hek293 cells as well as stable cell lines of Notch-containing and Delta-containing cells from Elowitz to observe the trans-activation of Notch by Delta. Other experiments using CHO cells, which are more difficult to transfect than Hek293 using Lipofectamine, were carried out to observe the behavior of CHO transfected cells.

Week 12: August 22 - Later

Stay tuned!

Week 12

September 1

Grant: Inoculations of the aforementioned LR constructs.

August 29

Charles - CHLRs see CH notebook. H, HL, T, U and delta-ff4, H and T for ncad-2a-eyfp. inoculated propagations for HLNcad2Aeyfp, UASNcad2aeyfp, and Tre:delta.

August 28

Grant: Restarted LR reactions of 9 of the constructs listed on the Workflow (only the pEXPR_12_Hef1a-LacO_Notch-CI434-VP16 construct succeeded, possibly due to incubation time for LR reactions). Started PCRs for Tango constructs using new padding for TEV cut site.

August 25

Divya: Won. (See Personal Notebook for details).

August 23

Charles - FACS Kens 50 50 and 80 20 Hek TRE-delta senders and CHO receivers. FACS was clean. Cells were all healthy. Lowered voltage of DAPI channel from 300 to 240 to move blank cells basal fluorescence to the bottom left corner. Laser was on, everything went according to plan. Preliminary results look promising, with increasing dox for each coculture, there was increasing FITC channel signal. Preliminary results suggest that our delta works.

August 22

Charles - FACS of Kens coculture stuff. Ambiguous results.