iGEM - International Genetically Engineered Machine

iGEM project 2023

The main concept of our project is to develop a bio-manufacturable lubricant gel which binds to target proteins on pathogen surfaces, thus immobilizing them and acting as a physical barrier for infection and transmission. The binding protein, its target, and consequently the target pathogen will be highly modular through AI-based protein design using RF Diffusion.

The main scope of usage for this product will be during sexual activities, thus preventing the spread of Sexually Transmitted Infections (STIs).

In addition, we see the possibility of our design approach being beneficial in clinical settings, e.g. prevention of Urinary Tract Infections (UTIs) during catheter insertion in hospital settings.

The WHO estimates that over 1 million STIs are acquired each day, with a high prevalence of viral STIs such as HSV and HPV which are highly infective and for which we have no cures available. While there are a few methods of contraception available currently, condoms remain the only way to truly reduce the rate of STI transmission, and these are still not considered to be 100% effective.

We hope that our project will provide a valuable tool in combating STIs, and also open up more conversation about what it truly means to practice safe sex, in the importance of preventing STIs alongside unwanted pregnancies.

igem2023-lab@cri-paris.org

https://2023.igem.wiki/paris-bettencourt/ 

Team Paris Bettencourt 2023

Louis Elverston

Louis Elverston

Leader

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Yoann Le Vay

Yoann Le Vay

HR

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Avishkar Jadhav

Avishkar Jadhav

Treasurer

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Laure Mourgue d'Algue

Laure Mourgue d'Algue

HR

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Stasa Rakocevic

Stasa Rakocevic

Designer

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Milena Milovanović

Milena Milovanović

Manager

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Tony Makdissy

Tony Makdissy

In silico/ dry lab

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Ernest Mordret

Ernest Mordret

Secondary PI

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Hritika Kathuria

Hritika Kathuria

Web Designer

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	Ariel Lindner

Ariel Lindner

Primary PI

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Mostafa Elraies

Mostafa Elraies

Mathematical and physical modelling

Amir Pandi

Amir Pandi

Advisor

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Former teams

2022

A synthetic biology toolkit to interface genetic circuits with electronics

Language originating from the field of electronics is often employed in synthetic biology to describe genetic logic circuits, meanwhile, the real intersection of electronics with genetics remains largely unexplored. Our iGEM team is developing a toolkit of genetic parts with the concomitant open-source hardware to enable synthetic biologists to interface bacterial gene expression with electronics. Our toolkit incorporates a multitude of genetic parts from previous research in electro-microbiology that have been standardised to allow for a wide variety of applications. We are conversely researching new means of bioelectronic control using hyperpolarization of bacterial membranes for gene induction. Our toolkit will open doors for foundational research in gene expression and control while finding applications in manufacturing, robotics, arts and new media.

Team Roster
Primary PI : Ariel Lindner
Secondary PI : Helena Shomar, Vincent Libis
Instructors : Francisco Javier Quero
Student Leaders : Michael Sedbon, Louise Destouches

Student Members :
Accion Vincent
Polina Rapoport
Timothée Leblond
Yves Loiseau-Marchand
Dounia Zedira

Florence Heng
Taylor Rayne
Daria Fedorova
Advisors : Juliette Bellengier, Clement Galan, Alexis Casas

2021

Mini.ink: think big, go with minicells

Biosafety is central when manipulating GMOs. We aim to participate in increasing biosafety by using minicells, nanosized and chromosome-free bacterial cells formed by abnormal division of rod-shaped bacteria. We observed their behaviour and hypothesized their use as chassis for local production of desired proteins, without purification expenses. This project is centered around the production of compounds through minicells of E.coli MG1655 containing a plasmid of interest. Minicells are produced using two approaches: overexpression of the FtsZ ring and deletion of the min operon. In parallel, a bioreactor for cultivation and isolation of minicells from parental cells was designed to guarantee a final genomic DNA-free sample. Filtration and introduction of an infection-defective lambda phage into the genome of parental cells was implemented to achieve higher separation yield. We focused the project on production of indigo pigment and found a method to safely dye textile without purification or addition of chemicals.

Team Roster
Primary PI : Edwin Wintermute, Ariel Lindner
Instructors : Aya Gomaa

Student Members :
Imran Nooraddin
Zoé Pincemaille
Juliette Bellengier
Sarah Haggenmueller
Clement Galan

Camila Ballenghien
Karolina Guzauskaite
Nathalia Raquel de Souza Fernandes
Daria Fedorova
Etienne LEMIERE
Advisors : Alexis Casas

2020

SynDerma : a foundational advance toward synthetic dermatology

In SynDerma we envisioned therapeutics being administered by engineered microbes integrated into the skin microbiome. First, to understand the perturbaility of the skin microbiome by individual habits such as hygiene, social interaction and exercise, which are all affected by this current unprecedented context of COVID-19 pandemia, we developed a community science project called Quaranskin. In Quaranskin we developed an at-home sampling kit, protocol and survey, where participants swabbed four body sites for metagenomic analysis. We correlated the diversity and composition of these collected microbiome data to behaviours noted in the surveys to uncover any trends. In parallel, we chose the skin commensal microbe Staphylococcus epidermidis to be a chassis for our future vision of microbial therapeutics enabled by synthetic biology. In projects EpiFlex, EpiGlow, and EpiGrow, we built a MoClo kit, expressed fluorescent proteins as a proof of concept, and optimised growth conditions, respectively.

Team Roster
Primary PI : Edwin Wintermute, Ariel Lindner

Student Members :
Chetan Kumar Velumurugan
Valerie March
Amandine Maire
Nikako Nikola Zarevski
Xavier Olessa-Daragon

Nicolas Levrier
Anu Susan kurian
Subham Choudhury

Advisors : Radoslaw Kamil Ejsmont, Darshak Bhatt, Alexis Casas

2018

STAR CORES: Protein scaffolds for star-shaped antimicrobial peptides

Antibiotic overuse in livestock industry is one of the major drivers to the antibiotic resistance evolution; motivating calls to reduce, replace, and re-think the antibiotic usage in animals. Antimicrobial peptides (AMPs) are a promising alternative to conventional antibiotics. Recently, a class of chemically-synthesized, star-shaped AMPs has been shown to exhibit broad-spectrum antimicrobial activity while maintaining biocompatibility with mammalian cells. In this project, we combinatorially fused a set of known AMPs to structurally diverse, self-assembling protein cores to produce star-shaped complexes. Over 200 fusions were designed and expressed in a cell-free system, then screened for activity, biocompatibility, and membrane selectivity. In addition, we selected 4 AMPs for rational mutagenesis (~12000 variants), and a subset of fusions for molecular dynamic modeling, to identify features of surface charge and star geometry that impact AMP performance. Overall, we aim to create a novel class of selective, non-toxic AMPs which are biologically-produced.

Team Roster
Primary PI : Ariel Lindner
Secondary PI : Edwin Wintermute
Instructors : Haotian Guo, Ana Santos, Gayetri Ramachandran
Student Leaders : Darshak Bhatt, Nympha Elisa M. Sia

Student Members :
Naina Goel
Annissa Ameziane
Juliette Delahaye
Camille Lambert
Alexis Casas

 

Santino NANINI
Antoine LEVRIER
Maksim Bakovic

Advisors : Oleksandra Sorokina

2017

Medusa: Bringing control to the 3rd dimension

Accurate spatial-temporal response is fundamental to synthetic biology. Optogenetics has emerged as a powerful tool for genetic control and Medusa brings optogenetics to the next level. By engineering E. coli to respond to multiple light inputs, creating a logical AND gate, we aim to achieve both spatial and temporal control of gene expression. Photosensory transmembrane proteins as well as photoswitchable protein caging were investigated to further expand the existing library of optogenetic tools. For spatial control at the subcellular level, we explored the use of a novel synthetic RNA organelles to manipulate enzymatic activity. Finally, in an effort to promote synthetic biology, we sought the input of the DIY community and chose to illustrate the power of our system by 3D-printing biomaterials.

Team Roster
Primary PI : Ariel Lindner
Secondary PI : Alvaro Banderas
Instructors : Haotian Guo
Student Leaders : Alma Chapet-Batlle

Student Members :
Joseph Ryan
Pierre-Luc Satin
Victor Pabst
Yulian Dobrev
Ianis Dobrev

 

Alicia Graham
Oleksandra Sorokina
Paul Cachera
Aya Gomaa

Advisors : Sophie Gontier, Prateek Garg

2016

Frank&Stain: Enzymetic alternatives to perchloroethylene for stain removal from fabrics

Dry cleaning is the removal of stains from delicate fabrics using solvents other than water. The most widely used solvent in dry cleaning is perchloroethylene (PERC), a volatile carcinogen that is increasingly banned and restricted for environmental and safety reasons. Our team is using synthetic biology to replace PERC with a biological alternative. To do so we are screening samples from all around the world to look for stain-digesting microbes, we are characterising candidate enzymes with putative stain digesting activity, and we are searching for fabric binding domains to enhance their stain fighting power! With some microbiology, synthetic biology, metabolic engineering and a lot of creativity we will find a green technology to make dry cleaners forget all about PERC.

Team Roster
Primary PI : Ariel Lindner
Secondary PI : Edwin Wintermute
Instructors : Jason Bland

Student Members :
Alicia Pereira e Calvo-Villamañán
Allison Bricknell George
Elisa Hubert
Antoine Villa
Sebastián Sosa Carrillo
HAOUCHINE Ibrahim

 

Shruthi Narayanan
Mislav Acman
Sébastien Gaultier
Mani Sai Suryateja Jammalamadaka
Thomas Meiller-Legrand

Advisors : Nadine Bongaerts

2015

Ferment It Yourself

Food fermentation is practiced by every culture in the world, and is especially widespread throughout the Indian subcontinent. Although fermentation enriches foods with some essential vitamins and amino acids, many regions of the subcontinent still suffer from high malnutrition. We are addressing this problem by engineering S. cerevisiae and lactobacilli, commonly found in Indian fermented rice dishes, to enrich foods with vitamins A, B2, and B12, and bioavailable iron.
We also implemented a differentiation system for reducing the fitness cost of over-expression of multiple pathways, and an easy E. coli sensor for measuring vitamin concentration using a riboswitch.
Our user-centered approach incorporates a low-cost and open hardware framework, both for growing and distributing starter cultures, and for quality control. This will give local affected populations power over their own food, as opposed to other GMO nutritional enrichment strategies, by allowing them to grow their own source of vitamins.

Team Roster
Primary PI : Ariel Lindner
Instructors : Jason Bland, Edwin Wintermute

Student Members :
Ewen Corre
Sophie Gontier
Barthelemy Caron
Arthur Molcard
jean baptiste caron
Prateek Garg
Antoine Vigouroux
Shazzad Hossain Mukit
Abdul-Salem Hadjadj-Aoul

 

Ferrando Jérémy
Célia Foulon
Amaury Monmeyran
Constant Bourdeloux
EMILIE TAVAN
Cloé Pierson

Advisors : Ihab Boulas, Juan Manuel GARCIA ARCOS

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