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Keywords
HIV, virology, protein stability, mutation effects
Abstract
Human immunodeficiency virus type 1 (HIV-1) is a retrovirus that infects CD4+ T cells. Without treatment, infection with HIV-1 usually leads to acquired immunodeficiency syndrome (AIDS), which is characterized as severe immunosuppression (CD4+ count: < 200cells/mm3 of blood). However, some individuals do not advance to AIDS and are known as long-term non-progressors (LTNP). Interestingly, a small viral protein of HIV-1, called viral protein R (Vpr), has been associated with HIV-1 progression. The R77Q mutant has been linked to the LTNP phenotype and increased levels of apoptosis; however, the mechanisms behind it are not yet understood [1]. Previously, our group has found that Vpr was expressed at lower levels in cells infected with R77Q virus compared to the wildtype (WT) virus by western blot [1]. Image quantification of the bands showed an approximate six-fold reduction in protein levels.
BYU ScholarsArchive Citation
Mason, Linnea; Sithole, Sidney T.; and Berges, Bradford K., "In Silico Studies of HIV-1 Vpr R77Q Mutant’s Structure and Stability" (2026). Library/Life Sciences Undergraduate Poster Competition 2026. 27.
https://scholarsarchive.byu.edu/library_studentposters_2026/27
Document Type
Poster
Publication Date
2026-03-26
Language
English
College
Life Sciences
Department
Microbiology and Molecular Biology
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