Michigan Synthetic Biology Team 2013 Introduction Mike Ferguson - - PowerPoint PPT Presentation

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Michigan Synthetic Biology Team 2013 Introduction Mike Ferguson - - PowerPoint PPT Presentation

Michigan Synthetic Biology Team 2013 Introduction Mike Ferguson What is a Transcriptor? What is its utility? Regulates flow of RNA polymerase across strand of DNA Used in logic gates Tightly controlled switch or as a storage device


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SLIDE 1

Michigan Synthetic Biology Team

2013

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SLIDE 2

Introduction

Mike Ferguson

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What is a Transcriptor? What is its utility?

Sources: Jerome Bonnet et al. Amplifying Genetic Logic Gates. Science 3 May 2013, Vol. 340 no. 6132 pp. 599-603. Jerome Bonnet, Pakpoom Subsoontorn, and Drew Endy. Rewritable digital data storage in live cells via engineered control of recombination directionality. PNAS. 2012 Apr 6.

Int/Ex Transcriptor Logic Gates

  • Regulates flow of RNA polymerase across strand of DNA
  • Used in logic gates
  • Tightly controlled switch or as a

storage device

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The Problem with Current Transcriptors

  • Recombination Directionality Factors
  • Not completely unidirectional

Source: Jerome Bonnet, Pakpoom Subsoontorn, and Drew Endy. Rewritable digital data storage in live cells via engineered control

  • f recombination directionality. PNAS. 2012 Apr 6.
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SLIDE 5

The Solution: Utilizing the Fim Switch

Source: M. P. McCusker, E. C. Turner and C. J. Dorman. DNA sequence heterogeneity in Fim tyrosine-integrase recombinase-binding elements and functional motif asymmetries determine the directionality of the fim genetic switch in Escherichia coli K-12. Molecular Microbiology, 67, 171–187.

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SLIDE 6

Caveat: DNA bending proteins and other Regulators

Source: I. C. Blomfield, D. H. Kulasekara and B.

  • I. Eisenstein. Integration host factor stimulates

both FimB- and FimE-mediated site-specific DNA inversion that controls phase variation of type 1 fimbriae expression in Escherichia coli. Molecular Microbiology (1997) 23(4), 705–717. Source: 2012 Michigan iGEM Source: Schwan WR. Regulation of fim genes in uropathogenic Escherichia coli. World J Clin Infect Dis 2011; 1(1): 17-25.

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SLIDE 7

Wet Lab: Design

Drew Dunham

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Switch Design and Sequence Determination

  • Conserving the LRP and IHF binding sites
  • Deletion of the most of the native fimA promoter

○ Allows for a switch with customizable promoter function insertion

Source: D. L. Gally, J. Leathart and I. C. Blomfield. Interaction of FimB and FimE with the fim switch that controls the phase variation of type 1 fimbriae in Escherichia coli K-12. Molecular Microbiology (1996) 21(4), 725–738.

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Assaying the Transistor: Chromophore Reporter

  • Utilization of multiple chromophore

reporters

○ GFP ■ Allows for easy quantification due to highly

characterized nature

■ Requires UV excitement to visualize ○ AmilCP ■ Easily visualized by the naked eye ■ Not a fluorescent protein

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SLIDE 10
  • Utilizing repeated restriction enzyme cut

sites to identify the state of the switch

Assaying the Transistor: Digest

B A A B

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SLIDE 11

Inducing Recombinase Activity

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Wet Lab: Results

Mike Ferguson

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The Fim Transcriptor is Capable of Changing States Completely and Unidirectionally

  • Constitutively expressed

fimE and hbiF flip the engineered switch completely

  • Faint bands may be due to

too high copy plasmid number

  • r the recombinase generator

itself in the case of the ON lane

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SLIDE 14

An Inducible Fim Transcriptor System Changes States and Produces Protein Output

  • Uninduced colonies show a mixed state
  • The switch can still produce protein
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SLIDE 15

Determination of Inducer Concentrations Necessary to Flip the Fim Transcriptor Completely

  • HSL flips the switch ON, producing

amilCP

  • aTc flips the switch OFF, producing

no protein

  • The color of the bacteria is not

enough to determine how efficient the state change was.

  • 7uM aTc flips the switch completely
  • The concentration of HSL still needs

to be determined.

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SLIDE 16

An Inducible Recombinase Generator is Capable of Cycling the State of the Fim Transcriptor

  • The fim transcriptor

can cycle states

  • The grayish color in 4B

may be due to incomplete protein degradation

  • Given more time, flipping

back to the OFF state does not show any residual amilCP

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SLIDE 17

Results Discussion

  • It works!
  • Need to do the digest assay on the cultures

with higher HSL concentrations

  • High copy plasmid may result in not all of

the switch being flipped

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SLIDE 18

Future Directions

Raoul Martin

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Future Directions

  • Chromosome integration
  • Eliminate the use of

high copy plasmid.

  • Integrate the switch in

the E. coli chromosome

  • The cell will only be

able to be in an “ON” or “OFF” state. Reasoning: Eliminate the chances of expressing “ON” and “OFF” switch states simultaneously.

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Future Directions

  • In vitro assay:

○ Purify both HbiF and FimE ○ Add one of the recombinases to a solution containing the switch plasmid. ○ PCR purification ○ PCR amplification Reasoning: This will enable us to check if HbiF and FimE are the only two proteins required for the switch to function.

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SLIDE 21

Dry Lab: Modeling

Joshua Abramson

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Switch Modeling

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SLIDE 23

Models

  • Expression model
  • Inducible Hbif model
  • Switch model
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SLIDE 24

Modeling Approach

  • Mass action differential equation systems
  • Analytical vs. numerical modeling
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SLIDE 25

ERSESCO Algorithm

  • 7. Optimization
  • 4. Equilibration
  • 6. Calibration
  • 5. Stabilization
  • 3. Solution
  • 2. Reduction
  • 1. Equation
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SLIDE 26

Switch Model

  • Two irreversible catalyses
  • Pseudo-steady state enzymes
  • Enzyme cooperativity
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Switch Model

  • Equation:
  • Reduction:
  • Solution:
  • Equilibration:
  • Stabilization:
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Switch Model

  • Calibration:
  • Optimization:
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Other Models

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Human Practice

Corey Howe

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  • University of Toledo, OH
  • Ocean and Ivor Huang
  • Talked modeling with Team Toulouse

WISE

  • Collaboration with U of M Program.
  • Women In Science and Engineering.
  • Experiments
  • Strawberry DNA extraction
  • Saliva DNA extraction and necklace
  • Gel Electrophoresis
  • Presentations and Quizzes.
  • Celebrity Crime Mystery

Outside Help

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SLIDE 32
  • Educational Platformer Video Game
  • Mobile App and Computer game
  • Plasmid Paul Character
  • Broad Audience Range
  • Original Soundtrack
  • Currently in Beta Version
  • Can be played on our Wiki Page

Adventures of Plasmid Paul

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SLIDE 33

Adventures of Plasmid Paul

Ligation Level Freezer Level Zombie News Freezer Level Incubator Level Mini-Prep Level Digestion Level Ligation Level PCR Level Gel Level Boss Level

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While 32 people played the game…

  • 83% of players enjoyed the time they spent.
  • 32% of players learned what a protein is.
  • 22% of players learned what a plasmid is.
  • 31% of players learned what synthetic biology is.
  • 66% of players interest in synthetic biology was sparked.
  • Before the game, 3% of the players thought synthetic biology was more

harmful than helpful to society, while after the game none of the players thought it was more harmful.

  • 10% changed their thoughts to think that synthetic

biology is safe.

  • 83% of players learned something from the game.

Results

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SLIDE 35

Conclusion

Jonah Sementkowski

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SLIDE 36
  • Created a working fim transcriptor and demonstrated greater

than 95% efficiency on a high copy plasmid

  • Developed an effective educational video game
  • Defined a new procedure for analysis of mathematical systems
  • Made the fim transcriptor easily customizable
  • Submitted a complete, inducible, fim transcriptor

system

  • Submitted characterization data for numerous new

and improved registry parts

Accomplishments

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SLIDE 37

Inducible fimE and hbiF recombinase generator (tet and lux) fim switch inverted repeat left (IRL) natural fim switch inverted repeat right (IRR) natural

Submitted Parts

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SLIDE 38

J23100 fim switch B0034 amilCP ON

  • rientation

J23100 fim switch B0034 GFP ON

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J23100 fim switch ON orientation Natural fim switch OFF orientation Natural fim switch B0034 GFP OFF

  • rientation

Submitted Parts

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Thank you!

Questions?