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HIV-1 Entry and Membrane Fusion Inhibitors.
Xiao, Tianshu; Cai, Yongfei; Chen, Bing.
Afiliación
  • Xiao T; Division of Molecular Medicine, Boston Children's Hospital, Boston, MA 02115, USA.
  • Cai Y; Department of Pediatrics, Harvard Medical School, Blackfan Street, Boston, MA 02115, USA.
  • Chen B; Division of Molecular Medicine, Boston Children's Hospital, Boston, MA 02115, USA.
Viruses ; 13(5)2021 04 23.
Article en En | MEDLINE | ID: mdl-33922579
HIV-1 (human immunodeficiency virus type 1) infection begins with the attachment of the virion to a host cell by its envelope glycoprotein (Env), which subsequently induces fusion of viral and cell membranes to allow viral entry. Upon binding to primary receptor CD4 and coreceptor (e.g., chemokine receptor CCR5 or CXCR4), Env undergoes large conformational changes and unleashes its fusogenic potential to drive the membrane fusion. The structural biology of HIV-1 Env and its complexes with the cellular receptors not only has advanced our knowledge of the molecular mechanism of how HIV-1 enters the host cells but also provided a structural basis for the rational design of fusion inhibitors as potential antiviral therapeutics. In this review, we summarize our latest understanding of the HIV-1 membrane fusion process and discuss related therapeutic strategies to block viral entry.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: VIH-1 / Inhibidores de Fusión de VIH / Internalización del Virus / Fusión de Membrana Límite: Humans Idioma: En Revista: Viruses Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: VIH-1 / Inhibidores de Fusión de VIH / Internalización del Virus / Fusión de Membrana Límite: Humans Idioma: En Revista: Viruses Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza