Presentation Outline

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'''Western Presentation'''
 
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* ''Define our goals''
 
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** Solve a mathematical problem using bacteria
 
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** Integrate math and biology students holistically
 
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** Work in tandem with two campuses to test parallel processing of PUIs for iGEM
 
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** Design a device that would be more than just a widget
 
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** Have a lot of fun learning
 
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* ''Introduction''
 
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** Synthetic biology
 
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*** tests our understanding of biological units and
 
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*** allows us to design new devices using DNA.
 
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** Define burnt pancake problem
 
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** Schematic design of 1, 2, 3, and 4 pancake stacks
 
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** Mathematics behind solution and possible number of flips per n pancakes
 
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** Describe Biological equivalent problem
 
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'''Bubble Topics - split as time demands'''
 
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* ''Methods''
 
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** Hin (+/- LVA)and Hix and RE and Fis (list of basic parts)
 
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** How to assemble small DNA segments too big for oligos (Lance’s web site)
 
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** How to generate backwards biobrick parts with PCR (switch-a-roo)
 
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** Modeling the behavior of pancake flipping – deducing kinetics and size biases
 
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** Using modeling to choose which families of pancake stacks to build
 
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** Distinguishing 1,2 from -2,1 → add in promoterless RFP
 
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'''Davidson Presentation'''
 
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* Data
 
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** Promoterless RBS+TF = tet resistant
 
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** Backwarks Tet + backwards RBS  = tet resistant
 
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** Therefore, pSB1A2 and 3 have readthrough transcription in both directions
 
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** Design and build pSB1A4 (describe construction and demonstrate function)
 
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** Combine Hix with 1 pancake stacks (promoter-flavored and coding-flavored)
 
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** Uncontrolled flipping
 
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** Western blot of Hin….
 
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** Building 2 pancakes….
 
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* Consequences of Devices:
 
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** Data storage
 
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** Improved transgenic organisms (two states)
 
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** Proof-of-concept for bacterial computers
 
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** Next steps
 
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* Conclusions
 
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** Can solve problem but need control over kinetics
 
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** Math and Biology meshed really well – even uncovered a new proof
 
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** Multiple campuses can increase capacity through communication and cooperation. Size of school is not a limiting factor.
 
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** First in vivo controlled flipping of DNA??
 
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** We had a blast and learned heaps.
 
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Things to keep in mind...
Things to keep in mind...
# We should have each team work as separate units to facilitate team spirit and ability to practice. However, we will share slides for continuity of presentations.  
# We should have each team work as separate units to facilitate team spirit and ability to practice. However, we will share slides for continuity of presentations.  

Latest revision as of 12:23, 9 October 2006

Things to keep in mind...

  1. We should have each team work as separate units to facilitate team spirit and ability to practice. However, we will share slides for continuity of presentations.
  2. We will probably have to let go of who did what in order to have two smooth presentations. We can have a color-coded schematic slide early on that shows where different parts were built but this does not affect who presents what. In fact, this chart will help people see how well the two schools worked in parallel.
  3. We need to have talks ready and two posters.

This outline is the one Karmella started and was edited by the Western team.

  • INTRODUCTION (MO Western)
    • Our goals
      • Solve a mathematical problem using bacteria
      • Integrate math and biology students holistically
      • Work in tandem with two campuses to test parallel processing of PUIs for iGEM
      • Design a device that would be more than just a widget
      • Have a lot of fun learning
    • Define the math problem: burnt pancake problem
    • The Hin recombinase system in Salmonella – flagellar antigen variation
    • Turning the Hin recombinase system into a BioBricks system - Hix, Hin, RE
    • Schematic design of 1 & 2 pancake stacks
    • Computing with E. coli - detecting orientation of DNA pancakes using the antibiotic resistance screen (two-pancake system, animation by Karmella)
    • Design of 4 pancake constructs
    • Mathematics behind solution and possible number of flips per n pancakes
    • Biological equivalence problem - will be solved using backwards RFP (described later)
  • METHODS (Western)
    • Building new parts - Hix, Hin, antibiotic genes, backwards parts
    • how we assembled small DNA segments too big for oligos (Lance’s web site)
    • how we generated backwards biobrick parts with PCR (switch-a-roo)
    • List of Basic Parts – Hin (+/- LVA), Hix, RE, etc.; end with this; highlight who did what
    • Transition to Data

--Kahaynes 15:49, 6 October 2006 (EDT) (below)

METHODS & DATA (Davidson)
Lance List of Basic Parts
Lance Modeling the behavior of pancake flipping – deducing kinetics and size biases
Lance Using modeling to choose which families of unsolved pancake stacks to start with
Erin Single pancakes - illustration, animation (Karmella) of pLac-Hin control by LacI/ IPTG, DNA flipping, and pBad control by AraC/ arabinose
Erin The problems of read-through - uncontrolled Tet expression, uncotrolled flipping (MO Western and Davidson data, Hin Western blot?)
Erin New pSB1A4 vector insulates, but A4 has cloning problems
Samantha Redesign - pancakes without TT's
Samantha Two pancake constructs
Samantha Biological equivalence - distinguishing 1,2 from -2,-1 using RFP-RBS, updated panckaes
CONCLUSIONS (Davidson)
Sabriya Consequences of devices - data storage, possible application for rearranging transgenes in vivo, proof-of-concept for bacterial computers, first in vivo controlled flipping of DNA??
Sabriya Next steps - can solve problem but need control over kinetics
Sabriya Lessons learned - troubleshooting, communication, teamwork, publicity; Math and Biology meshed really well and even uncovered a new proof; Multiple campuses can increase capacity through communication and cooperation; Size of school is not a limiting factor; We had a blast and learned heaps
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