PhD Student (M/F) in Molecular Biology for the Development of Inhibitory Aptamers and Detection of Matrix Metalloproteinases.
New
- FTC PhD student / Offer for thesis
- 36 months
- BAC+5
Offer at a glance
The Unit
Architecture et Réactivité de l'ARN
Contract Type
FTC PhD student / Offer for thesis
Working hHours
Full Time
Workplace
67084 STRASBOURG
Contract Duration
36 months
Date of Hire
01/10/2026
Remuneration
2300 € gross monthly
Apply Application Deadline : 28 July 2026 23:59
Job Description
Thesis Subject
Matrix metalloproteinases (MMPs) are key players in tissue remodeling and the regulation of certain biological mechanisms. Among these enzymes, MMP12, produced and secreted by macrophages, is particularly interesting due to its multiple roles. In addition to its canonical function as a secreted protease mediating the degradation of the extracellular matrix and certain cell surface receptors, MMP12 also exhibits several non-canonical "moonlighting" functions. Notably, the catalytic domain of the protein has been shown to regulate the expression of genes in the NF-κB pathway (involved in inflammation, among other processes) by directly binding to nuclear DNA. Furthermore, the free hemopexin-like domain of MMP12 has been demonstrated to possess antibacterial properties within lysosomes. Thus, not only the full MMP12 protein but also its individual domains exhibit varied functions depending on their state and localization.
This PhD project aims to deepen our understanding of the MMP12 system and dissect its complexities in greater detail through the development of new tools dedicated to imaging and/or targeted functional interference.
The main objective of the PhD work will be the identification of aptamers (oligonucleotides capable of specifically recognizing epitopes on proteins, analogous to antibodies) targeting the different domains of the protein (catalytic domain, hemopexin-like domain, either isolated or in combination). To achieve this, the candidate will use in vitro selection approaches (SELEX) to enrich large libraries of candidate oligonucleotides with molecules capable of specifically binding the target protein (or domain). The enriched libraries obtained will then be screened using high-throughput droplet microfluidics platforms developed by the team. This dual approach will enable the rapid and efficient isolation of two types of aptamers: i) Aptamers dedicated to imaging protein targets, achieved by coupling the aptamers to a fluorescent module developed by the team. ii) Inhibitory aptamers that, by strongly binding to the protein, will inhibit a targeted function (enzymatic activity, intracellular relocalization, DNA binding, depending on the intended function).
The combined use of these new molecular tools will enable a more in-depth and precise study of MMP12 under cellular conditions.
This doctoral project will be affiliated with the Doctoral School of Life and Health Sciences of Strasbourg (ED-414), which has validated it. Conducted in close collaboration with Laurent Devel's team (CEA), who will develop new chemical tools, this research project is funded by the French National Research Agency (ANR) and will begin in October 2026. To ensure an immediate start and efficient progress, the candidate must have in-depth knowledge of molecular biology and nucleic acid biochemistry, as well as prior experience in handling nucleic acids, particularly in in vitro selection. Additionally, the candidate should have basic knowledge of droplet microfluidics systems.
Your Work Environment
The PhD work will be carried out in the "Digital RNA Biology" team led by Michael Ryckelynck, based within the CNRS unit "Architecture et Réactivité de l'ARN" (Institute of Molecular and Cellular Biology, Strasbourg). The team has unique, internationally recognized expertise in developing and using droplet microfluidics combined with high-throughput sequencing for RNA studies and the directed evolution of fluorescent RNA aptamers for biotechnological applications. The team currently consists of three permanent researchers, one postdoctoral fellow, five PhD students, and three engineers.
The PhD student will have access to all the equipment and infrastructure necessary for the successful completion of the project. In addition to daily informal supervision and regular team laboratory meetings, weekly individual progress meetings will be organized with the thesis director. Several project follow-up meetings will also be held biannually within the consortium.
Moreover, the laboratory is located in close proximity to public transportation (including the tram) as well as university eating facilities. Additionally, no specific time constraints (such as staggered hours or other obligations) will be required for carrying out the mission.
For more information about the team and its activities, please visit the website: https://ibmc.cnrs.fr/en/laboratoire/arn-en/equipes/biologie-digitale-de-larn/
Constraints and risks
No specific constraints or risks are anticipated for this assignment.
Compensation and benefits
Compensation
2300 € gross monthly
Annual leave and RTT
44 jours
Remote Working practice and compensation
Pratique et indemnisation du TT
Transport
Prise en charge à 75% du coût et forfait mobilité durable jusqu’à 300€
About the offer
| Offer reference | UPR9002-MICRYC-014 |
|---|---|
| CN Section(s) / Research Area | Molecular and structural biology, biochemistry |
About the CNRS
The CNRS is a major player in fundamental research on a global scale. The CNRS is the only French organization active in all scientific fields. Its unique position as a multi-specialist allows it to bring together different disciplines to address the most important challenges of the contemporary world, in connection with the actors of change.
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