Title: Cling-E. coli : Bacteria on target
1Cling-E. coli Bacteria on target
Ellenor Brown Stephanie Lo Alex Pickett Sammy
Sambu
Kevin Shee Perry Tsai Shaunak Vankudre George Xu
2The motivationTo develop a system for targeting
bacteria to a specific substrate and effecting a
cellular response
3Potential Targets and Applications
Bind Proteins
Bind Toxins
Bind Tissue
Bind DNA/RNA
Bind Viruses
Bind Surface
Bind Other Cells
4Bacterial targeting
Quorum-sensing
Fec signal transduction
5Surface Engineered Bacteria Engineered to Bind
and Signal
6Selecting/enriching for surface engineered
bacteria
- Tags
- 6xHis nickel beads
- Strep2 streptavidin beads
7His/Strep2 tagged bacteria are enriched by MACS
(after MACS selection)
235 10 206 11
8Results Cell Selection Assays are a Success!
AIDA was re-engineered to target nickel and
streptavidin with 6xHis and Strep2 tags
respectively, and selecting for
surface-engineered bacteria was accomplished
through magnetic activated cell sorting.
9Bacterial targeting
Fec signal transduction
Quorum-sensing
10luxI/luxR Quorum Sensing
Receiver
Sender
11Cell-Cell Signaling Constructs
- Receivers (luxR Reporter)
- GFP Receivers
- tetR controlled (Bba_T9002)
- Quorum controlled (Bba_R0062 Bba_C0261
Bba_E0240) - mRFP Receivers
- tetR controlled (Bba_F2620 Bba_I13507)
- Quorum controlled (Bba_R0062 Bba_C0261
Bba_I13507) - mCherry Receivers (Bba_F2620 Bba_J06702)
- Senders (bicistronic luxI Reporter)
- mRFP Sender
- tetR controlled (Bba_S03623 Bba_I13507)
- lacI controlled (Bba_S03608 Bba_I13507)
- Quorum controlled (Bba_R0062 Bba_A340620
Bba_I13507) - GFP Sender
- tetR controlled (Bba_S03623 Bba_E0240)
- lacI controlled (Bba_S03608 Bba_E0240)
- Quorum controlled (Bba_R0062 Bba_A340620
Bba_E0240) - mCherry Sender
- tetR controlled (Bba_S03623 Bba_J06702)
12Switch-like Quorum Response
13Selection with Magnetic Beads
Sender
1460-fold Selection through Magnetic Beads
Control no beads
Selection with streptavidin beads
Green (untagged) Red (tagged)
15Enriched senders activate quorum response
16Bacterial targeting
Quorum-sensing
Fec signal transduction
17Motivation Fec System
- Goal Direct cell signaling
- Method Re-engineer an existing signal
transduction pathway - Fec system
- well-characterized
- substrate specific
18Overview of Fec System
Braun et al. Gene Regulation by Transmembrane
Signaling. Biometals 2006 Apr19(2)103-13.
19Overview of Fec System
Loops 7 8
20Constructs
- From Braun lab (U. Tuebingen, Germany)
- Fec knock-out strain, AA93
- FecIRA plasmid
- Fec promoter, GFP plasmid
- pColA Duet Vector
- Allows regulated expression of Fec genes under T7
promoter
21Wild-Type GFP Expression
22Troubleshooting andNext Steps
- Problems
- Growth media
- Toxicity membrane disruption?
- Goals
- Nickel and Streptavidin Binding
- Finding new targets with signaling
- Random library
- Computational Approach
23Conclusions
- Targeting
- His and Strep2 tags on AIDA, targeting bacteria
to nickel and streptavidin was successful - Quorum sensing
- Constructed one-cell system
- Characterized two-cell system
- Combined with targeting
- Fec signal transduction
- Characterized Fec system
24Future Directions
- Bacterial targeting
- Trying out new targeting peptides (calmodulin)
- Optimizing the random library approach in
selecting for targeting peptides - Quorum sensing
- Characterizing one-cell system
- Optimizing quorum response after targeting
- Fec signal transduction
- Effect signal transduction with targeting
- Application
25Acknowledgements
Advisors George Church Debra Auguste Jagesh V.
Shah William Shih Pamela Silver Alain Viel Tamara
Brenner
Teaching Fellows Nicholas Guido Bill
Senapedis Mike Strong Harris Wang
Funding HHMI Harvard Provost Harvard Life
Sciences Division Harvard School of Engineering
and Applied Sciences
Special thanks to Volkmar Braun (University of
Tuebingen) Costas Maranas (Penn State
University)