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Trials and Tribulations of a First Year iGEM Team Morgan Taschuk Newcastle University
Outline ,[object Object]
Ambitious project
Potholes
The Jamboree
Happy Ending
Questions
The Team Advisors Instructors Students
The Team ,[object Object]
And me
Wanted to shoot big!
Circle of (Synthetic) Life Feedback Implementation Computational Modelling Bioinformatics Tools Sequence Synthesize Clone Analyze
Circle of (Synthetic) Life ,[object Object]
Not “sexy”
No computational aspect ,[object Object],Feedback Implementation Computational Modelling Bioinformatics Tools Sequence Synthesize Clone Analyze
Sensing Bacteria ,[object Object]
Cell-cell communication
Sensing Bacteria ,[object Object]
Sensing Bacteria ,[object Object]
Sensing Bacteria ? ? ,[object Object]
Need to discriminate between fingerprints
Sensing Bacteria ,[object Object]
Need to discriminate between fingerprints
Limited outputs
In Vitro  Neural Nets  ,[object Object]
Where do we start??
Good Advice ,[object Object]
Wet lab booked from 4 August
No DNA designed ,[object Object]
Designed a BioBrick by hand
Synthesized it ,[object Object]
Bad timing May Jun Jul Aug Sept Oct Nov Apr
Bad timing May Jun Jul Aug Sept Oct Nov Apr Team
Bad timing May Jun Jul Aug Sept Oct Nov Apr Team
Bad timing May Jun Jul Aug Sept Oct Nov Apr Team
Bad timing May Jun Jul Aug Sept Oct Nov Apr Team Tasks
Bad timing May Jun Jul Aug Sept Oct Nov Apr Team Tasks
Bad timing May Jun Jul Aug Sept Oct Nov Apr Team Tasks
Bad timing May Jun Jul Aug Sept Oct Nov Apr Team Tasks
Tally ,[object Object]
Number of remaining students: 1
Unfinished tasks ,[object Object]
T-Shirts
Presentation
DNA submission
Only just about everything we're judged on!
Wiki ,[object Object],[object Object]
Ripped several theses apart
Organised lab journals
T-Shirts David Appleyard and iGEM
Part Characterisation ,[object Object]
Not all parts need to have DNA, or even work!
Poster ,[object Object]
Presentation ,[object Object]

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Trials and Tribulations of a First Year iGEM Team

Notes de l'éditeur

  1. First year iGEM – wanted to shoot big! Wanted something awesome, on
  2. Methicillin-resistant Staphylococcus aureus MRSA difficult to distinguish from other S. aureus Mostly they just grow up the culture and see if they die in response to methicillin and other antibiotics Not sexy, as one of our advisors called it! It's not big and awesome enough for iGEM. Can be accomplished using traditional biology No computational aspect. Most of instructors were from computing science, with interest in synthetic biology. Therefore, wanted to incorporate in silico with biology
  3. Quorum sensing Fingerprints: unique to species or even the strain Cell-to-cell communication, determine friend or foe Multiple detection Pull quorum self-sensing systems out of multiple bacteria and place it into a single B. subtilis genome Fingerprints can be very similar. Related strains may release the same signal peptides, but at different relative levels Limited outputs Practical consideration: only 3-4 fluorescent proteins can be used with any chance of detecting by eye
  4. Quorum sensing Fingerprints: unique to species or even the strain Cell-to-cell communication, determine friend or foe Multiple detection Pull quorum self-sensing systems out of multiple bacteria and place it into a single B. subtilis genome Fingerprints can be very similar. Related strains may release the same signal peptides, but at different relative levels Limited outputs Practical consideration: only 3-4 fluorescent proteins can be used with any chance of detecting by eye
  5. Quorum sensing Fingerprints: unique to species or even the strain Cell-to-cell communication, determine friend or foe Multiple detection Pull quorum self-sensing systems out of multiple bacteria and place it into a single B. subtilis genome Fingerprints can be very similar. Related strains may release the same signal peptides, but at different relative levels Limited outputs Practical consideration: only 3-4 fluorescent proteins can be used with any chance of detecting by eye
  6. Quorum sensing Fingerprints: unique to species or even the strain Cell-to-cell communication, determine friend or foe Multiple detection Pull quorum self-sensing systems out of multiple bacteria and place it into a single B. subtilis genome Fingerprints can be very similar. Related strains may release the same signal peptides, but at different relative levels Limited outputs Practical consideration: only 3-4 fluorescent proteins can be used with any chance of detecting by eye
  7. Quorum sensing Fingerprints: unique to species or even the strain Cell-to-cell communication, determine friend or foe Multiple detection Pull quorum self-sensing systems out of multiple bacteria and place it into a single B. subtilis genome Fingerprints can be very similar. Related strains may release the same signal peptides, but at different relative levels Limited outputs Practical consideration: only 3-4 fluorescent proteins can be used with any chance of detecting by eye
  8. Learned: Be very clear about commitments Communication! Have a contigency plan
  9. No computational tools were ready: Masters projects ran until beginning of August. Wet lab booked at the beginning of August. While this timetable initially seemed reasonable, there is an additional step between BioBrick design and testing it in the bacteria: DNA production. Since we were using B. subtilis, and our brick wasn't in the repository, opted to have it synthesized Designed a Brick by hand
  10. Mostly sandwiches, crisps, fruit Bagels for breakfast – I thought it was great, but some people were less pleased
  11. Although we considered the lack of real questions at the end a vicopry, we suspected it had to do with two things: 1) Our project was mostly a software project, but we tried hard to make it fit into another track 2) We didn't make any grandiose claims about curing cancer in order to enhance our presentation – we just told it like it was.