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Remote Control of Bacterial Chemotaxis UCSF iGEM Team 2006 Patrick Visperas Matthew Eames Eli Groban Ala Trusina Christopher Voigt, Tanja Kortemme, Chao.

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Presentation on theme: "Remote Control of Bacterial Chemotaxis UCSF iGEM Team 2006 Patrick Visperas Matthew Eames Eli Groban Ala Trusina Christopher Voigt, Tanja Kortemme, Chao."— Presentation transcript:

1 Remote Control of Bacterial Chemotaxis UCSF iGEM Team 2006 Patrick Visperas Matthew Eames Eli Groban Ala Trusina Christopher Voigt, Tanja Kortemme, Chao Tang, Chris Rao

2 Remote Control of a Bacterial Machine Goal Start

3 How Bacterial Chemotaxis Works Bacteria Swim Up Gradients concentration gradient No gradient CCW Glide Tumble ? CW How Chemotaxis is Observed Goulian Motility Assay (U Penn)

4 The Regulatory Network W A P~ Y A Y No CheW No Swimming

5 Binding Partners Orthogonal binding pair Tsr-CheW (Liu et al, 1991) We mapped these mutations onto the Tar-Chew complex Tar CheW

6 Tsr mutation can be mapped to Tar Gradient Aspartate point mutation in Tar* reduces motility to approximately 40% that of wild-type

7 Part Design New orthogonal signaling pairs “Codon randomization” is used to reuse scaffolds without fear of recombination

8 Chassis Engineering Build E. coli strain lacking all sensors and CheW, but retaining the other chemotaxis proteins tar tsr tap trg aer cheW Wild-type E. coli tar tsr tap trg aer cheW UU1250 (Parkinson, U Utah) UU  cheW tar tsr tap trg aer cheW cheW*tar*

9 Tested in UU1250 FimE IRL IRR IRL OUTPUT [ara] FimE Ptrc * rfp gfp MCS GREEN RED 0 0.3 1.2 5 [arabinose] (mM) % bacteria 1. The plasmid is unstable 2. The strain contains FimE/ FimB 2 Possible Problems Device Characterization: The Fim-Switch - ara + ara INPUT T. Ham, et al (2006)

10 - arabinose Phe Asp Constructed via DNA synthesis (DNA 2.0) System Design (11 kB)

11 Phe Asp + arabinose Constructed via DNA synthesis (DNA 2.0) - arabinose Phe Asp System Design (11 kB)

12 Results Gradient Gradient Aspartate Phenylalanine

13 Conclusions Orthogonal pairs are a rapid method to built signaling pathways that can operate simultaneously Chassis developed to rapidly screen for new protein- protein interactions Limited by the switch performance in this chassis Directional control could also be achieved by non- chemical inputs (light, radiation, etc)


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