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.

Inquiries: nguyeny@sas.upenn.edu

Location: Carolyn Hoff Lynch Lecture Hall

Inquiries: nguyeny@sas.upenn.edu

Location: Carolyn Hoff Lynch Lecture Hall

Inquiries: nguyeny@sas.upenn.edu

Location: Carolyn Hoff Lynch Lecture Hall

Inquiries: nguyeny@sas.upenn.edu

Location: Carolyn Hoff Lynch Lecture Hall

Abstract: Phospholipids are the major constituents of cellular membranes and also important signaling molecules. Because these hydrophobic metabolites are not directly genetically encoded, their detection and precise manipulation with traditional genetic methods is challenging. Therefore, chemical methods for detecting the biosynthesis and intracellular transport of lipids, as well as those for modulating their levels with a high degree of spatiotemporal control, are urgently needed.

Abstract: Phase separation compartmentalizes cells via the formation of membraneless organelles, also called biomolecular condensates. Phase separation influences many fundamental biological processes, from transcription to sorting of molecules and the stress response. Phase separation is mediated by a combination of associative and segregative phase transitions, or networking and a density transition, which together result in a percolated dense phase. Condensates therefore have emergent properties, i.e., properties that small complexes do not possess.

Abstract: "Rising human exposure to pathogens couples with increased antibiotic resistance and slow antibiotic development to pose a nearly insurmountable human health challenge. My work aims to discover novel proteins critical for pathogen survival, reveal important insights into their mechanisms, and develop chemical tools to modulate them. By focusing on pathogens with limited biosynthetic capabilities, we aim to discover novel antibiotic targets that are less likely to evade inhibitors.

Abstract: "The space of possible organic compounds is incredibly large and diverse, while the space of core biochemistry is relatively small, though also diverse. This talk will explore relations between those two chemical spaces vis-a-vis prebiotic chemistry, evolution and analytical chemistry, and how exploration of those two spaces can inform both the origins of life and medicinal chemistry."

Inquiries: nguyeny@sas.upenn.edu

Location: Carolyn Hoff Lynch Lecture Hall