Event

Abstract: The surface of a cell experiences frequent stretching and compression. The resulting membrane tension is converted to intracellular electrochemical signals via mechanosensitive proteins such as Piezo channels. Currently, our understanding of the subcellular sorting and activation of mechanosensitive proteins is still in its infancy. Moreover, mapping the spatiotemporal heterogeneity of cell membrane tension remains technically challenging. Further into the cell, membraneless organelles represent a new class of subcellular structures whose mechanical responses are determined by their interfacial tension and viscoelasticity: two material properties that play pivotal biological and pathological roles.  A major challenge lies in the quantification of these condensate material properties, especially in living cells.

 In this talk, I will first discuss our efforts towards quantifying the spatial dynamics of cell membrane tension. Next, I will present our recent progress in unraveling the intricate interplay between cell membrane properties and the subcellular behavior of mechanosensitive membrane proteins. Finally, I will describe our contribution to quantifying the material properties of biomolecular condensates involved in various neuronal functions. By decoding the mechanical signaling pathways from the cell surface to intracellular organelles, we aim to shed light on various mechanobiological and aging-related diseases.

Inquiries: nguyeny@sas.upenn.edu

Location: Carolyn Hoff Lynch Lecture Hall