Profile
Marc Johnson, PhD researches retroviral assembly, a biological process involving multiple viral and cellular actors from diverse locations within the cell. These actors converge at defined assembly sites to create and facilitate the egress of an infectious viral particle. Dr. Johnson utilizes the model retrovirus HIV‐1 to study the basic viral components targeted to viral assembly sites, including how cellular processes are usurped to aid in this process. Dr. Johnson’s lab is studying how viruses target their cytoplasmic structural proteins to the same assembly sites as their trans‐ membrane targeting/fusion glycoproteins. Research has led to the theory that viruses utilize a common glycoprotein targeting pathway/mechanism to drive viral incorporation. A better understanding of this process could lead to novel therapeutics against viruses as well as enhanced ability to custom design viruses for use in precision medicine applications. Additionally, Dr. Johnson’s lab studies the HIV-1 accessory protein Vpu. Inhibitors of Vpu activity could be an important component of therapies aimed at eliminating reservoirs of HIV infected cells (cure). Dr. Johnson’s lab has found that Vpu targets the viral glycoprotein from Gibbon ape Leukemia Virus (GaLV Env) and prevents it from being incorporated into HIV-1 viral particles. Dr. Johnson is currently developing several small molecules with anti-Vpu activity as potential therapeutics for HIV-1 infected patients.
Academic Information
Office
471C Bond Life Sciences Center
Columbia, MO 65211
United States
Research Interests
- Virology and Molecular Therapies
- Cell Biology
- HIV/ AIDS
- Intracellular Trafficking
- Structural Biology
- Virology
Education & Training
Post-Graduate School
1999, PhD, Oregon State University
In the News
Publications
- Salamango DJ, Alam KK, Burke DH, Johnson MC. 2016. In Vivo Analysis of Infectivity, Fusogenicity, and Incorporation of a Mutagenic Viral Glycoprotein Library Reveals Determinants for Virus Incorporation. J Virol.90(14):6502-14. doi: 10.1128/JVI.00804-16. PMID: 27147747
- Salamango DJ, Johnson MC. 2015. Characterizing the Murine Leukemia Virus Envelope Glycoprotein Membrane-Spanning Domain for Its Roles in Interface Alignment and Fusogenicity. J Virol.89(24):12492-500. doi: 10.1128/JVI.01901-15. PMID: 26446598
- Salamango DJ, Evans DA, Baluyot MF, Furlong JN, Johnson MC. 2013. Recombination can lead to spurious results in retroviral transduction with dually fluorescent reporter genes. J Virol. 87(24):13900-3. doi: 10.1128/JVI.02524-13. PMID: 24067983
- Janaka SK, Gregory DA, Johnson MC. 2013. Retrovirus glycoprotein functionality requires proper alignment of the ectodomain and the membrane-proximal cytoplasmic tail. J Virol. Dec;87(23):12805-13. doi: 10.1128/JVI.01847-13. PMID: 24049172