From 2007.igem.org

Revision as of 21:02, 25 October 2007

Harvard University 2007 iGEM Team
	Students Ellenor Brown Stephanie Lo Alexander Pickett Sammy Sambu Kevin Shee Perry Tsai Shaunak Vankudre George Xu Education Advisor Tamara Brenner	Teaching Fellows Nicholas Guido Bill Senapedis Mike Strong Harris Wang Faculty Advisors Debra Auguste George Church Jagesh Shah William Shih Pamela Silver Alain Viel

The Harvard University 2007 iGEM Team

This year Harvard's team consisted of eight undergraduate students, with backgrounds in molecular and cellular biology, biochemistry, engineering, and computer science. With the help of six faculty advisers and four teaching fellows, plus one education advisor, they devised and executed a single project with three subsections.

Cling-E. Coli

1. Bacterial Targeting
2. Quorum Sensing
3. Fec Signal Transduction

As of the end of the summer, we successfuly demonstrated enriched targeting with known tagged sender and receiver cells. Separately, we characterized the quorum system with multiple types of promoters and reporters. We are on our way toward a combined targeting-quorum system in the near future. In addition, targeting with random libraries to various substrates should also be achieved.

Eventually, our project may have applicability in medical imaging and localized drug synthesis and release. Theoretically, if our project is successful, we demonstrate that bacteria (or other microorganisms) can be targeted specifically to a certain tumor cell. At a certain density, quorum sensing may allow for the bacteria to emit a signal that can be detected by medical imaging devices. If the reporter gene encoded for drugs or vitamins, synthesis can also be evoked through enriched targeting. Furthermore, binding through a modified Fec system may allow for binding alone to transduce a signal and elicit a response in the cells.

Bacterial Targeting

Project Overview

• The motivation for this part of the project was to engineer bacteria to adhere to targets with a high degree of specificity.
• Initial targeting was done by displaying histidine and strep2 tags on the E. coli surface via fusion with LppOmpA and AIDA-1 vehicles, and screens were performed with binding to their known nickel and streptavidin targets, respectively.
• After characterization and high enrichment with these known substrates, random libraries were inserted into LppOmpA and AIDA-1 constructs for screening peptides with affinity for novel targets. As we proceed with this experiment, we hope to characterize sequences that lend specificity to calmodulin and EGF.
• We also tried to utilize the same enrichment strategy with cells that were cotransformed with both AIDA-1-fused tags and quorum-sensing genes (see below).

Methods

Results

Conclusions and future plans

References

Quorum Sensing

Project Overview

• The motivation for this part of the project was to effect downstream activity after E. coli bind to a particular substrate, using the luxI/luxR quorum-sensing system from Vibrio fischeri, which would turn on after the bacteria localize to the target.
• Lux quorum-sensing works like a system of sender and receiver. LuxI codes for a protein that catalyzes the synthesis of 3-oxo-hexanyl homoserine lactone, or OHHL, which can diffuse freely through the surface of E. coli into the environment and into other E. coli. LuxR encodes for a protein which does not diffuse across the membrane and, when bound to OHHL, upregulates the luxpR promoter. So luxI-producing bacteria (senders) produce OHHL that diffuses into luxR-producing bacteria (receivers) where OHHL and luxR turn on luxpR promoter. This only occurs at a certain concentration of OHHL, thus a certain concentration of cells (quorum) is required.
• Initial characterizations of the luxI/luxR system and quorum activity were made using GFP and RFP reporters. Two approaches were taken to quorum sensing. (1) A luxI/luxR production system in one cell would be simpler, but it's possible that the cells might self-induce. (2) luxI and luxR production in separate cells would ensure no self-induction, but it requires monitoring two populations of cells.

Methods

• To characterize quorum activity, constitutive RFP senders were mixed with constitutive receivers. Fluorescence and OD (cell density) readings were taken every 15 minutes. [http://openwetware.org/wiki/IGEM:Harvard/2007/Laboratory_Notebooks/Quorum_Sensing/Plate_Reader_Protocol The protocol] was adjusted as necessary according to what the exact desired experiment was.
• To characterize binding activity, RFP-senders with AIDA tags were mixed with constitutive GFP non-tagged cells. As a control, a portion of the mixed cells was plated pre-selection. Direct magnetic beads (TALON nickel, Qiagen streptactin) were used to enrich for the tagged-senders. Several washes were done in low concentration imidazole. After incubations with beads and washes, the mixture was plated and grown overnight, and cell counts were done to determine extent of enrichment. (A more detailed protocol [http://openwetware.org/wiki/Shlo/directmagneticprotocol available]).
• More detailed methods are available on our [http://openwetware.org/wiki/IGEM:Harvard/2007/Laboratory_Notebooks/Quorum_Sensing wiki].

Results

• We were able to demonstrate that the sender-receiver system in one cell was not self-inducing but acted with quorum activity.
• Quorum activity was also detected with the separate sender and receiver cells.
• In collaboration with the [http://openwetware.org/wiki/IGEM:Harvard/2007/Bacterial_Targeting bacterial targeting] subteam, we have evidence that red sender cells tagged with strep2 on the surface (cotransformed with constitutive RFP/luxI plasmid and AIDA-strep2 plasmid) are enriched by selection with streptavidin-coated beads, while green non-tagged cells are not.
• Quorum activity was demonstrated as well through a plate-drop experiment.
• [http://openwetware.org/wiki/Shlo/flmicroprotstickiness Microscopy] was also used to detect and image tagged bacteria accumulating around beads, while non-tagged bacteria did not aggregate.

Enrichment by selection with magnetic beads

Fluorescence data indicates quorum activity

Microscopy images show tagged, red-sender cells accumulate around the beads, whereas the background green cells did not

Quorum activity was demonstrated via magnetically enriched sender cells that were plated on a receiver plate.

Conclusions and future plans

• Continue characterization of single cell constructs (approach (1) under Project Overview).
• Characterize cell and bead density require to reach quorum levels. We have been attempting to do this through Nickel-coated 96 well plates.

References

• Voigt CA. Genetic parts to program bacteria. Curr Opin Biotechnol 2006 Oct; 17(5) 548-57. doi:10.1016/j.copbio.2006.09.001 pmid:16978856.
• Anderson JC, Clarke EJ, Arkin AP, and Voigt CA. Environmentally controlled invasion of cancer cells by engineered bacteria. J Mol Biol 2006 Jan 27; 355(4) 619-27. doi:10.1016/j.jmb.2005.10.076 pmid:16330045
• Basu S, Mehreja R, Thiberge S, Chen MT, and Weiss R. Spatiotemporal control of gene expression with pulse-generating networks. Proc Natl Acad Sci U S A. 2004 Apr 27;101(17):6355-60.
• Sayut DJ, Niu Y, Sun L. Construction and engineering of positive feedback loops. ACS Chem Biol. 2006 Dec 20;1(11):681-2.

Fec Signal Transduction

Project Overview

• The motivation for this part of the project was to create a system such that a cellular response occurs when E. coli binds to a target ligand.
  

• We began by searching for known E.Coli signalling systems. The Fec system was chosen because it is the only known and well characterized signalling system with an outermembrane receptor. Most others responded to substrates that diffuse into the periplasm and bind to inner membrane proteins. This would be a very limiting mechanism for targetting.
  

• Fec System Overview:
  • The Fec system receptor is the outer membrane protein FecA. Its wild-type ligand is ferric citrate.
  • When binding occurs in iron-limiting conditions, a signal is sent to the inner membrane protein FecR.
  • FecR activates sigma factor FecI.
  • FecI is then used to induce gene expression.
    

• Structural papers detail the conformational changes that FecA undergoes when binding to ferric citrate.
  • The alpha helix in loop 7 unravels, and the loop moves by up to 11 angstroms
  • Loop 8 moves up to 15 angstroms.
• The motion of these two loops closes over the ferric citrate.
  

• These large changes suggest the importance of loops 7 and 8 to binding. From this, we proposed three options to modify the binding of FecA and hopefully maintain signalling:
  
  • Inserting a binding sequence into loop 7 (for simplicity and time, we arbitrarily chose to use either 7 or 8, and ended up using loop 7) of FecA such that it would bind to a new target at least, and produce a signal at most. To start, we chose 6xHis and Strep as binding sequences for nickel and streptavidin, respectively.
  • A computational approach which would produce nucleotide sequences for binding our new target. A directed mutagenesis of FecA would follow.
  • Use of random libraries to find binding sequences for given targets.

Methods

• Our first approach was to insert the binding sequences into FecA
  
• The main constructs used were shipped from researcher Volkmar Braun who conducted research on the Fec system at the University of Tuebingen in Germany. The constructs obtained were:
  
  • 1) AA93 E.Coli strain which does not express the Fec system
  • 2) A GFP plasmid with a Fec promotor and,
  • 3) pLCIRA, a plasmid containing the Fec system genes.
    
• This constructs were necessary because in order to test the binding of our re-engineered FecA, we would need to find a system or strain of E.Coli such that the natural Fec genes would be knocked out and only our re-engineering FecA would be expressed.
• Because pLCIRA is not well characterized and the expression of the Fec system is under its own promoter and upregulates itself upon binding, we thought it valuable to be able to control levels of FecA expression. So, we attempted to use a T7 pColA duet vector. However, AA93 is not a T7 cell, so we used lysogenization to make AA93 DE3 cells.
  
• We then inserted FecI&R (pcr'ed from the pLCIRA) into the first cloning site of the pColA plasmid and FecA (also pcr'ed from pLCIRA) into the second.

For more details, see the Harvard iGEM page...

Results

Conclusions and future plans

References

Click the picture, or click [http://openwetware.org/wiki/IGEM:Harvard here] for the more detailed Harvard iGEM 2007 wiki.