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Please use this identifier to cite or link to this item: http://hdl.handle.net/10451/6748

Título: Anti-HIV-1 antibodies 2F5 and 4E10 interact differently with lipids to bind their epitopes
Autor: Franquelim, Henri G.
Chiantia, Salvatore
Veiga, Ana Salomé
Santos, Nuno C.
Schwille, Petra
Castanho, Miguel A. R. B.
Palavras-chave: 2F5
4E10
gp41
HIV-1
Membrane proximal external region
Microscopy
Issue Date: 2011
Editora: Lippincott Williams & Wilkins
Citação: AIDS 2011, 25:419–428
Resumo: Objectives: 2F5 and 4E10 are two broadly neutralizing monoclonal antibodies (mAbs) targeting the membrane proximal external region (MPER) of HIV-1 gp41 envelope protein. This region, which contacts the viral membrane, is highly conserved and has been regarded as a promising target for vaccine development. We aimed to clarify the basis of 2F5 and 4E10 molecular interactions with epitope cores in MPER and lipid bilayers. Design: Microscopy-based approaches were used to infer and quantify the effects of both mAbs on membranes, in the presence and absence of the epitope cores. Supported lipid bilayers (SLBs), with and without phase separation, were used as membrane models. Fluorescent-labeled and nonlabeled MPER-derived peptides containing both 2F5 and 4E10 epitopes were used. Methods: mAbs 2F5 and 4E10 membrane interactions, in the presence or absence of MPER-derived peptides, were evaluated by combined atomic force and confocal microscopies. Results: Both mAbs form lipid-segregated aggregates on SLBs and do not induce other significant membrane perturbations. Furthermore, the affinity of MPER toward membranes is differently affected by both mAbs and correlates with the mAbs–epitope core lipid interactions. 2F5 is able to dock the MPER peptide on the membrane, whereas 4E10 extracts the MPER from the lipid bilayer. Conclusion: The results reveal the molecular details underneath 2F5/4E10 membraneepitope binding and a model is proposed to explain the differential mAbs neutralization efficacies, which relates to the exposure of the epitopes in the lipid bilayers and the role of the lipids in mAb–epitope binding.
Descrição: © 2011 Wolters Kluwer Health | Lippincott Williams & Wilkins
Arbitragem científica: yes
URI: http://dx.doi.org/10.1097/QAD.0b013e328342ff11
http://hdl.handle.net/10451/6748
ISSN: 0269-9370
Appears in Collections:IMM - Artigos em Revistas Internacionais

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