Team:NYU Abu Dhabi/Documentation/DOCS 20ee279bfcdc46b09c4fb108851b2757/Biology 93d1eff7b0cd4d6ca8529879e773d615/Meeting Notes 493bb338068540f8940ad3d462242538/August 5th 4e44f2cceb4e457d9695d7ca9bcf0404

August 5th

August 5th

@Yujeong Oh @Adrian Villanueva @Antonina Bar

Presentation:

Notes:

  1. Gene of choice
  • ITS region; need approval from Hussain to test in the lab because this contains the coding part
  • email him a short paragraph explaining what ITS region is and overall plan for our project. Ask for approval whether we can test this in the lab

2. Reporting mechanism

  • Fluorescence: Combine prof Song's fluorescence concentrator in our device
  • Ibrahim suggested one person from the engineering to work on this

3. Fall semester Lab work plan & suggestion

*Suggestions

  • Gene fragment (gBlock, our target gene)
    • instead of ligated into pJET vector (blunt-end ligation)
    • research on one-step insertion of the gene fragment (gBlock) into the E. Coli
  • Request meeting with Prof Youssef or his postdoc/ researcher
    • they are working on detection of COVID using fluidigm on RT-PCR
    • more sensitive than governmental/ official testing
    • ask him to share how they are doing
    • ask for whether we can work with them/ their method on our few samples
    • if allowed, order the reagents needed in their method
  • Request meeting with Prof AJ
    • ask him about nucleic acid detection
    • we previously tried to contact him, but didn't receive an reply

*Lab plans & advices

  • Specificity test: PCR/RPA/LAMP on miniprepped sample
    • test on gel to check specificity of the primers
  • Sensitivity test: PCR/RPA/LAMP on serial diluted miniprepped sample
    • test it on gel and with SYBR green
    • one might be more sensitive than others
  • LAMP has high negative control contamination
  • what are we detecting? DNA region vs. RNA region
    • ITS region is DNA region.
    • Do we need to work on RNA region?
    • For working with RNA, high number of samples are needed. Sometimes, the researchers work with the plasmid that express the RNA
      • work with BL21 E.coli strain (not DH-alpha) that express and transcribe DNA to RNA
  • Due to time restriction and budget cut, Ibrahim suggested us to focus on working with DNA detection this year
  • On wiki, we can list down the reseaches that we've done on detection of DNA and RNA.
    • add in the wiki that this might be a 2 year project and the following RNA detection part will be done in wet lab the following year.
  • Indeed, we can still experiment CRISPR-Cas13 using T7 transcription
    • post amplifcation → T7 transcription → CRISPR-Cas13
    • more research is required in this method
    • Things to consider: CRISPR-Cas13 is more sensitive than Cas12. Is it important? Do the detection require that sensitivity? How about time taken including T7 transcription step?
    • This should be discussed with faculties. Ibrahim strongly suggested us to have a meeting with faculties soon; if the general meeting cannot be scheduled, at least have a meeting from biology team.

4. Order

  • $10,000 allocated for bio and engineering orders
  • this is 1/6 of the previous year's order budget. This makes us harder to order all reagents that we want to order
  • We went over the order sheet together and marked the uncertain orders as yellow
  • If no payment is required for iGEM from now - september, place the order soon (within two days)

5. Future Plan

  • Parts (medal requirement)
    • our primers & gBlocks will be enough for new part characterization
    • Add documentation to existing part: do literature review on 2-3 existing parts and find & add new information
    • as a backup, Ibrahim suggested the engineering team to work on this criteria (i.e. design something for our project using 3D printer and take a video on how to make it).
  • Cost anlaysis
  • Computational analysis
  • Real sample testing is worth it to test in lab
    • To show our proof of concept (one of gold medal criteria)
    • It will be also nice to integrate biology parts with the engineering device to show the proof of concept
    • one person from biology team should work on the sample procurement

Next Steps:

*These are the next steps that I could think of after the meeting, please let me know if there are somethings else :)

  1. Email & Get approval from Hussain
  1. Research a method to insert the gBlock into E. coli DH-alpha plasmid without using pJET ligation
  1. Request meeting with Prof Youssef
  1. Request meeting with Prof AJ
  1. Research more on T7 transcription and SHERLOCK on DNA detection
  1. Schedule a faculty meeting to decide whether we will test SHERLOCK method
  1. Sample procurement from the German researcher
  1. Cost analysis
  1. Computational analysis
  1. Documentation on existing parts : literature reviews
  1. Follow up with Jeff & Place the order