Publication Date
12-7-2018
Document Type
Dissertation/Thesis
First Advisor
Hagen, Timothy J.
Degree Name
B.S. (Bachelor of Science)
Legacy Department
Department of Chemistry and Biochemistry
Abstract
Numerous studies have shown that Hepatitis C virus (HCV) and Dengue virus (DENV) are from the same family and have many characteristics in common. Despite the similarities, no adequate vaccines or antivirals have been developed for DENV yet although many are commercially available for HCV. In this research, we investigated the relationship between HCV and DENV, especially their NS3/4A and NS2B/3 proteases, to aid in the development of antiviral against DENV. To achieve this, in-depth structural analyses of the complexes were conducted; and molecular modeling stimulation software were utilized to visualize the interactions of the enzymes with different potential inhibitors including a potent inhibitor, Aprotinin. All peptoids derived bound to the active site of the enzyme complex near the catalytic triad although the interactions were not as strong as those in Aprotinin itself. Nonetheless, they demonstrate a good potential to for targeting the NS2B/3 protease. Further optimizations include increasing the rigidity of the structure through cyclization and eliminating residues that do not participate in the interaction with the enzyme.
Recommended Citation
Cheng, Thimoro, "Investigation of Dengue Virus (DENV) NS2B/3 Protease for Antiviral Development" (2018). Honors Capstones. 695.
https://huskiecommons.lib.niu.edu/studentengagement-honorscapstones/695
Extent
12 pages
Language
eng
Publisher
Northern Illinois University
Rights Statement
In Copyright
Rights Statement 2
NIU theses are protected by copyright. They may be viewed from Huskie Commons for any purpose, but reproduction or distribution in any format is prohibited without the written permission of the authors.
Media Type
Text