Structure-based Design of Broadly Neutralizing HCV Antibody and Vaccine
Authors
Pierce, Brian G.Boucher, Elisabeth N.
Smith, Heidi L.
Thomas, William D. Jr.
Weng, Zhiping
Wang, Yang
Document Type
Poster AbstractPublication Date
2014-05-20Keywords
BioinformaticsImmunoprophylaxis and Therapy
Therapeutics
Translational Medical Research
Virus Diseases
Metadata
Show full item recordAbstract
Hepatitis C virus (HCV) chronically infects nearly 200 million people worldwide. Antibodies have the potential to prevent establishment of chronic HCV infection in individuals exposed to the virus. Several broadly neutralizing monoclonal antibodies capable of binding HCV surface glycoproteins have been identified, including HCV1 identified by MassBiologics at UMMS, which targets a highly conserved linear epitope. We utilized the recently solved structure of the HCV1-bound epitope to identify regions of the antibody that could be modified to potentially improve binding to a mutation (N415K) which facilitates escape from neutralization. Based on systematic in silico mutagenesis of HCV1 residues in the Rosetta protein modeling program, a number of single or double antibody mutants were selected for in vitro evaluation. The mutated antibodies were synthesized and their ability to neutralize HCV pseudoviruses expressing either wild-type epitope sequence or the N415K variant was evaluated. Antibodies with mutations on the heavy chain, R65Q and V50L, demonstrated improved neutralizing activity against the N415K escape mutant without impacting their ability to neutralize wild type virus. We also sought to design a novel HCV vaccine that could focus the response to a small conserved neutralizing epitope of the virus defined by HCV1. The HCV1 epitope structure was used to search a large dataset of known protein structures from the Protein Data Bank, resulting in designs of scaffolds that were predicted to stably accommodate the epitope. These epitope-presenting scaffold proteins have been made and will be screened in animal studies to determine their potential as vaccine candidates for HCV prevention.DOI
10.13028/0ac1-0z20Permanent Link to this Item
http://hdl.handle.net/20.500.14038/27916Notes
Abstract of poster presented at the 2014 UMass Center for Clinical and Translational Science Research Retreat, held on May 20, 2014 at the University of Massachusetts Medical School, Worcester, Mass.
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Copyright the Author(s)Distribution License
http://creativecommons.org/licenses/by-nc-sa/3.0/ae974a485f413a2113503eed53cd6c53
10.13028/0ac1-0z20