Exploration of HIV-1 fusion peptide-antibody VRC34.01 binding reveals fundamental neutralization sites
Antibody binding to a vulnerable site of HIV envelope glycoprotein (Env), the eight N-terminal residues of the gp41 fusion peptide, renders robust HIV neutralization. Here, we theoretically investigate HIV-1 fusion peptide binding to the neutralizing antibody N123-VRC34.01. We explore numerous fusio...
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Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2019-08, Vol.21 (34), p.18569-18576 |
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creator | Feng, Mei Bell, David R Kang, Hongsuk Shao, Qiwen Zhou, Ruhong |
description | Antibody binding to a vulnerable site of HIV envelope glycoprotein (Env), the eight N-terminal residues of the gp41 fusion peptide, renders robust HIV neutralization. Here, we theoretically investigate HIV-1 fusion peptide binding to the neutralizing antibody N123-VRC34.01. We explore numerous fusion peptide mutations using all-atom molecular dynamics simulation with explicit-solvent models. Simulation results show that the hydrophobic interaction between Ile515 in the HIV-1 fusion peptide and the antibody VRC34.01 Fab plays an important role in antibody binding. Furthermore, we verify by free energy perturbation (FEP) calculations that two point mutations of Ile515Thr or Ile515Ala can dramatically weaken the binding affinity. Our findings provide new insights into fusion peptide-VRC34.01 binding, which can ultimately be utilized to design effective HIV vaccines. |
doi_str_mv | 10.1039/c9cp02909e |
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Here, we theoretically investigate HIV-1 fusion peptide binding to the neutralizing antibody N123-VRC34.01. We explore numerous fusion peptide mutations using all-atom molecular dynamics simulation with explicit-solvent models. Simulation results show that the hydrophobic interaction between Ile515 in the HIV-1 fusion peptide and the antibody VRC34.01 Fab plays an important role in antibody binding. Furthermore, we verify by free energy perturbation (FEP) calculations that two point mutations of Ile515Thr or Ile515Ala can dramatically weaken the binding affinity. Our findings provide new insights into fusion peptide-VRC34.01 binding, which can ultimately be utilized to design effective HIV vaccines.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/c9cp02909e</identifier><identifier>PMID: 31411214</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Antibodies ; Binding ; Computer simulation ; Free energy ; Glycoproteins ; Hydrophobicity ; Inhibitor drugs ; Molecular dynamics ; Mutation ; Peptides ; Perturbation methods ; Vaccines</subject><ispartof>Physical chemistry chemical physics : PCCP, 2019-08, Vol.21 (34), p.18569-18576</ispartof><rights>Copyright Royal Society of Chemistry 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-332c703d55165c8ab794024ab79afaa93f12df1564937daeecda52a0dca0cbf43</citedby><cites>FETCH-LOGICAL-c352t-332c703d55165c8ab794024ab79afaa93f12df1564937daeecda52a0dca0cbf43</cites><orcidid>0000-0001-8624-5591 ; 0000-0001-7115-3061</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31411214$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feng, Mei</creatorcontrib><creatorcontrib>Bell, David R</creatorcontrib><creatorcontrib>Kang, Hongsuk</creatorcontrib><creatorcontrib>Shao, Qiwen</creatorcontrib><creatorcontrib>Zhou, Ruhong</creatorcontrib><title>Exploration of HIV-1 fusion peptide-antibody VRC34.01 binding reveals fundamental neutralization sites</title><title>Physical chemistry chemical physics : PCCP</title><addtitle>Phys Chem Chem Phys</addtitle><description>Antibody binding to a vulnerable site of HIV envelope glycoprotein (Env), the eight N-terminal residues of the gp41 fusion peptide, renders robust HIV neutralization. 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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Antibodies Binding Computer simulation Free energy Glycoproteins Hydrophobicity Inhibitor drugs Molecular dynamics Mutation Peptides Perturbation methods Vaccines |
title | Exploration of HIV-1 fusion peptide-antibody VRC34.01 binding reveals fundamental neutralization sites |
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