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Multiple Sclerosis Triggers from a Biophysical Perspective
Rona Shaharabani [1] , Roy Beck [1] , Maor Ram-On [2] , Yeshayahu Talmon [2]
[1] Tel Aviv University, Tel Aviv, Israel, 6997801.
[2] Technion-Israel Institute of Technology, Haifa, Israel, 3200003.
Like electrical wires, the nerve cells in the body are coated with an insulating layer called myelin sheaths. In multiple sclerosis (MS) disease, the immune system mistakenly identifies the myelin as invading pathogens and attacks them. Once the protective sheaths are damaged, the nerves are essentially "short circuited", leading to versatile neurodegenerative symptoms. From the biophysical perspective, the myelin sheaths are a tightly packed, multilayered lipid-protein complex. The key hurdle in modelling such biological systems originates from complex interactions between multiple components. Physical models and experiments often reduce the number of components aiming to address the fundamental mechanisms. Nevertheless, in most cases, the inherent heterogeneity is an essential ingredient in the biological context. Here, we tackled the complex biological system of myelin sheaths, taking into account the heterogeneous lipids mixture, its relevant adhesive protein, and the environmental condition. Using synchrotron small angle X-ray scattering and direct cryogenic transmission electron microscopy, we performed structural measurements on model systems mimicking cytoplasmic myelin sheath complexes. Alteration in lipids composition, as in the MS diseased state, results in structural instabilities and phase transition from healthy lamellar to diseased inverted hexagonal structures. We also find that buffer salinity and temperature affect the self-assembly structures and result in the same pathological phase transition. In this talk I wish to map the delicate and complicated force balance between the myelin sheaths constituents and their effects on the structure of the composite system. This may help us understand the onset of instability in the transition to the diseased state, postulate on de-novo drugs, and the disease’s mechanism pathways.
(1) Rona Shaharabani, Maor Ram-On, Ram Avinery, Rina Aharoni, Ruth Arnon, Yeshayahu Talmon & Roy Beck, Pathological role of inverted hexagonal phase transition in disrupted myelin membranes. JACS, 138 (37), pp 12159–1216 (2016).
(2) Rona Shaharabani, Maor Ram-On, Yeshayahu Talmon & Roy Beck, Pathological transitions in myelin membrane derived by environmental conditions: a biophysical approach to multiple sclerosis, in preparation, (2017).