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Institute of Genetics and Molecular and Cellular Biology in France invites applications for a PhD position to study the structural and mechanistic basis of TIP60 Complex function in chromatin regulation and genome integrity. The project integrates cryo-EM, biochemistry, cell biology, and computational drug discovery.
The successful candidate will join an international team and access state-of-the-art facilities and a three-year contract with potential fourth-year extension, starting 1 Dec 2026.
Institute of Genetics and Molecular and Cellular Biology
Organisation/Company Institute of Genetics and Molecular and Cellular Biology Department Integrated Structural biology Research Field Chemistry » Biochemistry Biological sciences » Biology Medical sciences » Cancer research Researcher Profile First Stage Researcher (R1) Positions PhD Positions Application Deadline 15 Oct 2026 - 09:30 (Europe/Luxembourg) Country France Type of Contract Temporary Job Status Full-time Hours Per Week 38 Offer Starting Date 1 Dec 2026 Is the job funded through the EU Research Framework Programme? Not funded by a EU programme Is the Job related to staff position within a Research Infrastructure? No
PhD position:Structural and Mechanistic Basis of TIP60 Complex Function in Chromatin Regulation and Genome Integrity
Background
TheTIP60/EP400 complex (TIP60-C)is a highly conserved 20-subunit chromatin remodeling complex that plays fundamental roles in gene transcription and the maintenance of genome integrity. Through its lysine acetyltransferase (KAT) activity, TIP60-C acetylates histones H4 and H2A to promote chromatin relaxation, while its EP400 ATPase subunit catalyzes the exchange of canonical H2A for the histone variant H2A.Z, thereby regulating chromatin dynamics during transcription and DNA damage repair.
Beyond chromatin regulation, TIP60-C acts as a central signaling hub that coordinates diverse cellular processes, including DNA repair, immune responses, cell cycle progression, apoptosis, autophagy, metabolism, and development. These functions are mediated through the acetylation of both histone and non-histone substrates, which modulates protein activity, stability, and molecular interactions. Dysregulation of TIP60-C is implicated in numerous human diseases, including cancer, neurodegenerative disorders, and viral infections, making it a compelling therapeutic target.
Our laboratory recently solved the high-resolution cryo-EM structure of the endogenous human TIP60 complex ( https://www.nature.com/articles/s41586-024-08011-w ), providing an unprecedented view of its molecular architecture. This PhD position builds directly on that breakthrough.
Project Aims
Approach
The project integrates structural biology, biochemistry, cell biology, and computational drug discovery. The successful candidate will employ an interdisciplinary approach, combining single-particle cryo-electron microscopy, structure-based virtual screening, AI-driven de novo peptide and mini-protein design, biochemical characterization, and cellular functional assays.
Candidate Profile
What We Offer