AMOLF

Kristina Ganzinger Group

Immune cell signaling and bottom-up reconstitution of cell signaling in synthetic cells 

Kép

Our Focus

Signaling processes between various immune cells involve large-scale spatial reorganization of receptors and signalling molecules within the cell-cell junctions. These structures, now collectively referred to as immune synapses, interleave physical and mechanical processes with the cascades of chemical reactions that constitute signal transduction systems. Molecular level clustering, spatial exclusion, and long-range directed transport are all key regulatory mechanisms. Our group’s approach is based on advanced microscopy and on synthetic biology. We combine signalling pathway reconstitution with single-molecule biophysics to understand how immune cells communicate with each other and cancer cells: how do immune cells use molecular signalling pathways to transmit, process, and respond to information, both precisely and unambiguously? Currently, most projects in the lab use a hybrid in vitro-in vivo approach, interfacing in vitro cell surface models with immune cells. We use this approach to study the spatiotemporal reorganization of immune cell signalling molecules in natural signalling networks, but also for and man-designed signalling molecules in ImmunoTherapeutics against cancer.  

About Kristina Ganzinger

Members

Kristina Ganzinger
Scientific group leader
Chikim (Chi) Nguyen    
Phd student
Gerard Linares    
Postdoc
Megan Farrell    
Post-doc
Nebojsa Jukic    
Postdoc
Raquel Martinez Gonzalez    
Postdoc
Stefanos Zoidis    
PhD student
Tom Aarts    
Phd student