Elias Adriaenssens

Research Group “Mitochondrial Biology”

Research - Brief summary

Our lab studies how cells protect themselves against mitochondrial damage and maintain a healthy population of these essential organelles. Mitochondria are constantly exposed to damage and stress, so cells must identify and remove dysfunctional mitochondria while preserving the healthy mitochondrial network. Failure of these quality control mechanisms is linked to a wide range of human diseases, from Parkinson’s disease to life-threatening inherited mitochondrial disorders, underscoring the importance of understanding how cells maintain mitochondrial health. 

We are interested in discovering the molecular mechanisms that protect mitochondria from damage and maintain their function. Cells have evolved multiple layers of mitochondrial quality control, from preventing and repairing damage at the level of individual components to selectively removing mitochondria when damage can no longer be contained. We seek to understand how cells sense mitochondrial damage, decide when and how to intervene, and ultimately determine whether damaged mitochondria can be repaired or must be removed. 

Our lab combines biochemical reconstitution, cell biology and structural biology approaches to understand these processes from the molecular to the cellular level. We move between cells and purified systems to identify the molecular machinery that protects mitochondria and dissect the mechanisms underlying mitochondrial quality control. By rebuilding mitochondrial quality control pathways in vitro, we can study these processes in a simplified system and connect their molecular mechanisms to their function in cells. Through this combination of approaches, we seek to understand how cells preserve mitochondrial health and why these protective mechanisms fail in disease. 

Curriculum Vitae

Since 2025Postdoctoral Fellow in the lab of Tim Clausen 
Research Institute of Molecular Pathology (IMP), Vienna, Austria
2021 - 2025Postdoctoral Fellow in the lab of Sascha Martens 
Max Perutz Labs, Vienna, Austria 
2020 - 2021Postdoctoral Fellow in the lab of Vincent Timmerman 
University of Antwerp, Antwerp, Belgium
2014 - 2019PhD in the lab of Vincent Timmerman
University of Antwerp, Belgium 

Fellowships and Grants
2026ERC Starting Grant
2026Countdown Research Grant 
2022Marie Skłodowska-Curie Actions (MSCA) Postdoctoral Fellowship 
2021Instruct-ERIC Pilot Grant
2020FWO Junior Postdoctoral Fellowship
2020EPIC-XS Grant 


Selected publications

Adriaenssens E, Schaar S, Cook ASI, Stuke JFM, Sawa Makarska J, Nguyen TN, Ren X, Schuschnig M, Romanov J, Khuu G, Uoselis L, Lazarou M, Hummer G, Hurley JH, Martens S.
Reconstitution of BNIP3/NIX-mitophagy initiation reveals hierarchical flexibility of the autophagy machinery.
Nat Cell Biol. 2025 Aug;27(8):1272-1287.
Adriaenssens E*, Nguyen TN*, Sawa-Makarska J, Khuu G, Schuschnig M, Shoebridge S, Watts EM, Csalyi KD, Padman BS, Lazarou M, Martens S.
Control of mitophagy initiation and progression by the TBK1 adaptors NAP1 and SINTBAD.
Nat Struct Mol Biol. 2024 Nov;31(11):1717-1731. ​​​​​​​
Adriaenssens E, Asselbergh B, Rivera-Mejías P, Bervoets S, Vendredy L, De Winter V, Spaas K, de Rycke R, van Isterdael G, Impens F, Langer T, Timmerman V.
Small heat shock proteins operate as molecular chaperones in the mitochondrial intermembrane space.
Nat Cell Biol. 2023 Mar;25(3): 467-480.
Alderson TR*, Adriaenssens E*, Asselbergh B, Pritišanac I, Van Lent J, Gastall HY, Wälti MA, Louis JM, Timmerman V, Baldwin AJ, Benesch JLP.
A weakened interface in the P182L variant of HSP27 associated with severe Charcot-Marie-Tooth neuropathy causes aberrant binding to interacting proteins.
EMBO J. 2021 Apr 15;40(8):e103811.
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