| Literature DB >> 26715302 |
Dezhi Li1,2, Jie Liu2, Li Zhang2, Tianshu Xu2,3, Junheng Chen2,3, Liping Wang4, Qi Zhao5,6.
Abstract
The Human immunodeficiency virus type 1 (HIV-1) gp41 membrane proximal external region (MPER) is targeted by broadly neutralizing antibodies (e.g. 2F5, 4E10, Z13e and m66.6), which makes this region a promising target for vaccine design. One strategy to elicit neutralizing antibodies against the MPER epitope is to design peptide immunogens mimicking neutralization structures. To probe 2F5-like neutralizing antibodies, two yeast-displayed antibody libraries from peripheral blood mononuclear cells from a HIV-1 patient were screened against the 2F5 epitope peptide SP62. Two 2F5-like antibodies were identified that specifically recognized SP62. However, these antibodies only weakly neutralized HIV-1 primary isolates. The epitopes recognized by these two 2F5-like antibodies include not only the 2F5 epitope (amino acids (aa) 662-667 in the MPER) but also several other residues (aa 652-655) locating at the N-terminus in SP62. Experimental results suggest that residues of SP62 adjacent to the 2F5 epitope influence the response of broadly neutralizing 2F5-like antibodies in vaccination. Our findings may aid the design of vaccine immunogens and development of therapeutics against HIV-1 infection.Entities:
Keywords: 2F5; HIV-1; membrane proximal external region (MPER); neutralizing antibody; yeast display
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Year: 2015 PMID: 26715302 PMCID: PMC8200909 DOI: 10.1007/s12250-015-3664-6
Source DB: PubMed Journal: Virol Sin ISSN: 1995-820X Impact factor: 4.327