Overall project

In our project, we aim to utilize a microbe that responds to conditions in human body as an approach to administer smart peptide-based therapies. GLP-1, a human innate neuro-peptide for energy balance, is chosen to combat for obesity and metabolic syndrome. We engineer the non-pathogenic E. coli which senses fatty acids in intestines and secretes synthetic GLP-1. Appropriate signal peptides and penetratin are used to facilitate peptide secretion and intestinal uptake. Furthermore, we design a circuit with quorum sensing and double repressors, which aims to generate quick but sustainable responses and serves as an anti-noise filter. Plasmid stabilization modules including partition system and multimer resolution system are also incorporated to circumvent the undesirable loss or segregational instability of our artificial device. With this general concept of delivery of short peptide into human body, we can also target other human diseases with alternative circuit designs.

Project Details

hormone therapy-body weight control

Background

Design

CPP File:Https://www.dropbox.com/s/1lnt1d2uo401rz6/123.mov fadR

Modeling

Results

Extension

peptide2

Background

Design

Modeling

Results

Extension

delivery circuit

Background

Design

Modeling

Results

Extension

Stability of delivery system

Briefing

As our system will function outside the labrotory and human gut lack for antibiotic selection pressure, the vector stability is the critical point that determine whether our system is applicable or not. Inspired by natural plasmid & transposable gene element, we cope up with vector instability by incorporating partition system, Multimer resolution system and toxin antitoxin system these modules into our design.

Background

plasmid instability

multimer resolution system

A description list is perfect for defining terms.

partition system

A description list is perfect for defining terms.

Post-segregation killing

A description list is perfect for defining terms.

Design

multimer resolution system:Tn1000(gamma delta) resolution system

partition system:from pseudomonas putida KT2440

Post-segregation killing:srnBC toxin-antitoxin system

reference

• 1.reference one
• 2.reference two

safety of delivery system

suicidal system:

     Level 1 of column

Many turn off strategies have been developed, most of these are the inducible suicide system that can be activated at certain condition. For instance, in our project, we plan to use temperature and small molecule as activating signals( following picture). When the course of treatment ends administration of small amount of tetracycline agonist will induce bacterial death, leaving human body also cause suicide gene activation thereby avoid recombinant strain/gene pollutiing. And splitting suicide system to provide repression in trans can prevent plasmid transfering to wild type strains.

However, these design cannot totally eliminate the risk of horizontal gene transfer(HGT), which recombinant genes can move to other organisms independent of suicide system. So besides suicide system, we come up with a new idea to deal with these kinds of HGT risks by RNA interaction!!!

Expression well designed antisense RNAs have been shown to have inhibitory effect on paired RNAs, putting appropriate antisense RNAs on untranslated region of transcripts may interfere target RNA function or translation. We can use this tool to prevent HGT. For instance, laboratory E.coli have inactivated all its hok/sok toxin-antitoxin system by mutation, but wild bacteria especially pathogenic bacteria have many active TA locus on its chromosome like E.coli O157 have many active hok/sok homologs. HGT is more likely to occur between related species, we plan to put a stem loop from hok mRNA which can interact with sok RNA 5’sequence on UTR of antibiotic resistance genes we used. IF wild E.coli steal our antibiotic resistance genes and express it, its antitoxin will be competitive inhibited and its toxin will express and kill the thief thus preventing HGT between lab & wild coli. This idea is can have wide extension. Besides targeting antitoxin (functional RNA) of type I TA. We can also design antisense sequences that target RBS then we can down regulate target protein. Type II TA and essential genes for metabolism can also be targets Even if the In the past the repression efficiencies of antisense RNA in bacteria are low, but by using the paired termini antisense RNA method and incorporate U turn/YUNR motif,

Modeling

Results

Extension