Date of Award
Fall 12-18-2012
Degree Type
Thesis
Degree Name
Bachelor of Science (BS)
Department
Biology
First Advisor
Dr. Irene Weber
Abstract
Human Immunodeficiency Virus (HIV) has become a global pandemic with at least 25 million deaths and no cure. One of the most important targets to inhibit this virus is HIV-1 protease (PR), which is required to cleave the viral proteins needed for maturation of the virus after it invades and replicates in the host cell. There are nine protease inhibitors that are used in AIDS treatment. The virus loses susceptibility to these inhibitors by drug resistance due to mutations. The goal of the project is to examine the highly drug resistant HIV PR P51 in its complex with inhibitors. In this experiment we expressed and purified HIV PR P51 protein. We performed protein crystallization with inhibitors Tipranavir, Amprenavir, Darunavir, and Saquinavir to obtain the structure of the protease and the inhibitors in their complexes. Future analysis of the crystal structures will help with the development of successful therapeutic inhibitors.
DOI
https://doi.org/10.57709/3555693
Recommended Citation
Greene, Shaquita T. and Zhang, Ying, "HIV-1 PR P51 Mutant Complex Formation with Inhibitors." Thesis, Georgia State University, 2012.
doi: https://doi.org/10.57709/3555693