Lauren Slosky

Assistant Professor University of Minnesota

Lauren Slosky is an Assistant Professor in the Department of Pharmacology and a member of the Medical Discovery Team on Addiction, a multidisciplinary initiative within the University of Minnesota’s Medical School to advance research and treatment in the field of drug addiction. Dr. Slosky’s research is focused on understanding how neuropeptide G protein-coupled receptors regulate reward, pain, and motivated behavior – and how these receptors can be targeted for therapeutic benefit. She is currently working to identify novel strategies for the treatment of stimulant and opioid addictions, with a focus on the development of allosteric and functionally selective small molecules. Dr. Slosky was awarded a B.S. with honors in Molecular and Cellular Biology and Psychology from The University of Arizona in 2011. She received a Ph.D. in Medical Pharmacology from The University of Arizona in 2015, under the mentorship of Dr. Todd W. Vanderah. Dr. Slosky completed a postdoctoral fellowship in the laboratory of Dr. Marc G. Caron at Duke University and joined the Department of Pharmacology as an Assistant Professor in 2021.

Seminars

Wednesday 29th April 2026
Targeting the Intracellular GPCR Core: A New Paradigm for Rationally Designing Biased Neuropeptide Ligands
2:45 pm
  • Identifying a conserved intracellular allosteric pocket on GPCRs, to design small molecules that directly modulate G-protein engagement, enabling unusually strong and clean pathway-selective signaling bias
  • Selectively restricting or promoting access of specific transducers at the GPCR core, to allow rational tuning of signaling outputs, achieving desired therapeutic pathways while minimizing on-target side effects
  • Leveraging a pocket that is conserved yet structurally variable across the GPCR superfamily, to provide a scalable framework for tailoring receptor-specific biased ligands and discovering new activities guided by ternary-complex insight
Wednesday 29th April 2026
Panel Discussion: Assessing the Pharmacological Impact of Biased Signaling, Endosomal Pathways & Oligomerization to Demystify GPCR Complexity
12:15 pm
  • What are the innovative methodologies to study biased, endosomal, and oligomeric GPCR signaling?
  • How can we establish best practices for interpreting complex signaling data and distinguishing true pharmacological effects?
  • How to translate mechanistic insights into improved GPCRs-targeted drug discovery and development
Lauren Slosky