Functional and Structural Characterization of Human V3-Specific Monoclonal Antibody 2424 with Neutralizing Activity against HIV-1 JRFL
Abstract
The V3 region of HIV-1 gp120 is important for virus-coreceptor interaction and highly immunogenic. Although most anti-V3 antibodies neutralize only the sensitive tier 1 viruses, anti-V3 antibodies effective against the more resistant viruses exist, and a better understanding of these antibodies and their epitopes would be beneficial for the development of novel vaccine immunogens against HIV. The HIV-1 isolate JRFL with its cryptic V3 is resistant to most V3-specific monoclonal antibodies (MAbs). However, the V3 MAb 2424 achieves 100% neutralization against JRFL. 2424 is encoded by IGHV3-53 and IGLV2-28 genes, a pairing rarely used by the other V3 MAbs. 2424 also has distinct binding and neutralization profiles. Studies of 2424-mediated neutralization of JRFL produced with a mannosidase inhibitor further revealed that its neutralizing activity is unaffected by the glycan composition of the virus envelope. To understand the distinct activity of 2424, we determined the crystal structure of 2424 Fab in complex with a JRFL V3 peptide and showed that the 2424 epitope is located at the tip of the V3 crown (307IHIGPGRAFYT319), dominated by interactions with HisP308, ProP313, and ArgP315. The binding mode of 2424 is similar to that of the well-characterized MAb 447-52D, although 2424 is more side chainmore »
- Authors:
-
- Veterans Affairs New York Harbor Healthcare System, New York, NY (United States); NYU School of Medicine, New York, NY (United States)
- NYU School of Medicine, NY (United States)
- Veterans Affairs New York Harbor Healthcare System, New York, NY (United States); NYU School of Medicine, New York, NY (United States); Univ. de Strasbourg (France)
- Harvard Medical School, Boston, MA (United States)
- Publication Date:
- Research Org.:
- Argonne National Lab. (ANL), Argonne, IL (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES); National Institutes of Health (NIH); National Cancer Inst.; National Inst. of General Medical Sciences
- OSTI Identifier:
- 1213730
- Grant/Contract Number:
- AC02-06CH11357; AI102740; AI100151; AI082274; Y1-CO-1020; Y1-GM-1104
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Journal of Virology
- Additional Journal Information:
- Journal Volume: 89; Journal Issue: 17; Journal ID: ISSN 0022-538X
- Publisher:
- American Society for Microbiology
- Country of Publication:
- United States
- Language:
- ENGLISH
- Subject:
- 59 BASIC BIOLOGICAL SCIENCES
Citation Formats
Kumar, Rajnish, Pan, Ruimin, Upadhyay, Chitra, Mayr, Luzia, Cohen, Sandra, Wang, Xiao-Hong, Balasubramanian, Preetha, Nádas, Arthur, Seaman, Michael S., Zolla-Pazner, Susan, Gorny, Miroslaw K., Kong, Xiang-Peng, and Hioe, Catarina E. Functional and Structural Characterization of Human V3-Specific Monoclonal Antibody 2424 with Neutralizing Activity against HIV-1 JRFL. United States: N. p., 2015.
Web. doi:10.1128/JVI.01280-15.
Kumar, Rajnish, Pan, Ruimin, Upadhyay, Chitra, Mayr, Luzia, Cohen, Sandra, Wang, Xiao-Hong, Balasubramanian, Preetha, Nádas, Arthur, Seaman, Michael S., Zolla-Pazner, Susan, Gorny, Miroslaw K., Kong, Xiang-Peng, & Hioe, Catarina E. Functional and Structural Characterization of Human V3-Specific Monoclonal Antibody 2424 with Neutralizing Activity against HIV-1 JRFL. United States. https://doi.org/10.1128/JVI.01280-15
Kumar, Rajnish, Pan, Ruimin, Upadhyay, Chitra, Mayr, Luzia, Cohen, Sandra, Wang, Xiao-Hong, Balasubramanian, Preetha, Nádas, Arthur, Seaman, Michael S., Zolla-Pazner, Susan, Gorny, Miroslaw K., Kong, Xiang-Peng, and Hioe, Catarina E. Wed .
"Functional and Structural Characterization of Human V3-Specific Monoclonal Antibody 2424 with Neutralizing Activity against HIV-1 JRFL". United States. https://doi.org/10.1128/JVI.01280-15. https://www.osti.gov/servlets/purl/1213730.
@article{osti_1213730,
title = {Functional and Structural Characterization of Human V3-Specific Monoclonal Antibody 2424 with Neutralizing Activity against HIV-1 JRFL},
author = {Kumar, Rajnish and Pan, Ruimin and Upadhyay, Chitra and Mayr, Luzia and Cohen, Sandra and Wang, Xiao-Hong and Balasubramanian, Preetha and Nádas, Arthur and Seaman, Michael S. and Zolla-Pazner, Susan and Gorny, Miroslaw K. and Kong, Xiang-Peng and Hioe, Catarina E.},
abstractNote = {The V3 region of HIV-1 gp120 is important for virus-coreceptor interaction and highly immunogenic. Although most anti-V3 antibodies neutralize only the sensitive tier 1 viruses, anti-V3 antibodies effective against the more resistant viruses exist, and a better understanding of these antibodies and their epitopes would be beneficial for the development of novel vaccine immunogens against HIV. The HIV-1 isolate JRFL with its cryptic V3 is resistant to most V3-specific monoclonal antibodies (MAbs). However, the V3 MAb 2424 achieves 100% neutralization against JRFL. 2424 is encoded by IGHV3-53 and IGLV2-28 genes, a pairing rarely used by the other V3 MAbs. 2424 also has distinct binding and neutralization profiles. Studies of 2424-mediated neutralization of JRFL produced with a mannosidase inhibitor further revealed that its neutralizing activity is unaffected by the glycan composition of the virus envelope. To understand the distinct activity of 2424, we determined the crystal structure of 2424 Fab in complex with a JRFL V3 peptide and showed that the 2424 epitope is located at the tip of the V3 crown (307IHIGPGRAFYT319), dominated by interactions with HisP308, ProP313, and ArgP315. The binding mode of 2424 is similar to that of the well-characterized MAb 447-52D, although 2424 is more side chain dependent. The 2424 epitope is focused on the very apex of V3, away from nearby glycans, facilitating antibody access. Lastly, this feature distinguishes the 2424 epitope from the other V3 crown epitopes and indicates that the tip of V3 is a potential site to target and incorporate into HIV vaccine immunogens.},
doi = {10.1128/JVI.01280-15},
journal = {Journal of Virology},
number = 17,
volume = 89,
place = {United States},
year = {Wed Jun 24 00:00:00 EDT 2015},
month = {Wed Jun 24 00:00:00 EDT 2015}
}
Web of Science
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