Neurotransmission relies on the tight spatial and temporal regulation of the synaptic vesicle (SV) cycle. The average nerve terminal contains large amounts of presynaptic proteins, above 100 mg/ml according to quantitative analyses, and SVs, mitochondria and other organelles occupy nearly half of the volume of the nerve terminal. We are fascinated by how cytosol remains soluble to allow metabolic processes to occur concomitantly in space and time. The goal of Milovanovic Lab is to understand: How is the spatial organization of organelles and macromolecules regulated in the crowded environment of the cytosol at the nerve terminal?
We hypothesize that the presence of intrinsically disordered regions (IDRs)–low amino acid complexity sequences that do not fold into any stable secondary or tertiary structure—plays an essential role in balancing the solubility with the spatial patterning. Many proteins involved in the synaptic vesicle recycling contain long IDRs. Recently, it was shown that synapsin 1, a highly abundant synaptic protein, forms a distinct liquid phase in an aqueous environment (Fig. 1) (Milovanovic et al., 2018). Synapsin condensates are reaction centers able to sequester lipid vesicles. This mechanism helped to explain how hundreds of SVs are kept into distinct clusters while maintaining their high mobility (Milovanovic and De Camilli, 2017).
Significance. Given the central roles of proteins with IDRs in the pathology of many neurodegenerative diseases, our work will open new diagnostic and therapeutic strategies to combat these diseases. For example, a-synuclein is involved in a family of diseases that include Parkinson's and Dementia with Lewy Bodies and contains an IDR. Tau, another neuronal protein that contains an IDR, is associated with Alzheimer's disease. Neuronal RNA-binding proteins such as hnRNPA1, FUS, TDP43 are all linked to Amyotrophic Lateral Sclerosis and Frontotemporal Dementia and contain IDRs. Classically, the hallmark of the abovementioned neurodegenerative diseases is misfolding and aggregation of these proteins/their IDRs. Strikingly, the recent analysis of human postmortem brain tissues of Parkinson's patients shows that aggregates are, in fact, a crowded medley of vesicular structures. Hence, it is of crucial importance to understand the underlying mechanisms that keep these central organellar components soluble and functional in the crowded environment of the nerve terminal.
We stand for the education through research. Therefore, we gladly host students and trainees.
Thus far, lab alumni include:
Antonela Condric (Free University of Berlin, DE, 2022)
Lona Lion (University of Maastricht, NL, 2021)
Gwendolin Schneider (Free University of Berlin, DE, 2021)
Chinyere Logan (Free University of Berlin, DE, 2020-2021)
Linda Kokwaro (Charité University Medical Center, DE, 2021)
Franziska Trnka (Free University of Berlin, DE, 2021-2022)
Guiseppe Morabito (PhD at the University of Milano Bicocca, IT; 2020-2021)
Erasmus and internship students:
Shyline Bajaba (Jacobs University Bremen, DE, 2021)
Sila Kara (Middle East Technical University, TK, 2022)
Jean-Baptiste Moog (University of Paris Saclay, FR, 2022)
Ema Novakova (IMS FH Krema, AT, 2021-2022)
Additionally, we regularly host rotation students from the Medical Neuroscience Program at Charité and the Einstein Center for Neurosciences in Berlin.