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Nevin Lambert

Regents' Professor

Nevin Lambert

Regents' Professor

Professor

Academic Appointment(s)

Medical College of Georgia
Department of Pharmacology and Toxicology

Administration
Department of The »Æ¹Ï¶ÌÊÓÆµ School

Other Duties

Vice Chair, Pharmacology and Toxicology

  • NELAMBERT@augusta.edu
  • (706) 721-6336
  • CB 3522

Education

  • Ph.D., Neuroscience Kent State University, 1991

  • BS, Science Teacher Education/General Science Teacher Education Youngstown State University, 1990

Courses Taught Most Recent Academic Year

  • MEDI 6120

    Foundations of Medicine
  • BIOM 8022

    Molecular Cell Biology
  • MEDI 6130

    Musculoskeletal/Skin
  • PHRM 8042

    Pharmacology & Therapeutics I
  • PHRM 9020

    Seminar in Pharmacology
  • CURS 4990

    Undergrad Research III
  • MEDI 6220

    Cardiopulmonary/Heme
  • MEDI 6240

    GI/GU/Endocrine
  • PHRM 8043

    Pharmacology & Therapeutics II
  • PHRM 5003

    Pharmacology Tutorial

Teaching Interests

In addition to training future scientists at the bench I am involved in teaching pharmacological principles to medical and graduate students in the classroom, and case-based learning to medical students in small groups.

Scholarship

Selected Recent Publications

  • Amylin receptor subunit interactions are modulated by agonists and determine signaling., 2025
    Journal Article, Academic Journal
  • An integrated mechanism of G q regulation of PLCβ enzymes, 2025
    Journal Article, Academic Journal
  • Visualization of endogenous G proteins on endosomes and other organelles, 2024
    Journal Article, Academic Journal
  • GLP-1R signaling neighborhoods associate with the susceptibility to adverse drug reactions of incretin mimetics., 2023
    Journal Article, Academic Journal
  • In-Cell Arrestin-Receptor Interaction Assays., 2023
    Journal Article, Academic Journal

Research Interests

My lab’s long-term objective is to understand how G protein-coupled receptors (GPCRs), heterotrimeric G proteins and other signaling proteins interact, and how these proteins are organized in specialized cells to produce physiological responses. Much of what we do requires the development of optical tools for imaging and spectroscopy in living cells, often taking advantage of rapid advances in structural biology, protein engineering and chemical biology. As specific examples, we engineered a resonance energy transfer (FRET and BRET) sensor to detect G protein activation (free Gbg subunits) in living cells, chemical and physical methods to immobilize and trap GPCRs in artificial microdomains on the cell surface, and a BRET method to monitor the subcellular trafficking of membrane proteins in real time. We have used these tools to gain insights into the process of receptor-G protein coupling and preassembly, G protein heterotrimer dissociation, the regulation of signaling kinetics by RGS proteins, and the quaternary structure of GPCRs. These methods have also been successfully adopted by many other labs.

College Service

  • 2023 - 2023

  • 2023 - 2023

  • 2023 - 2023

  • 2022 - 2023

  • 2010 - 2023