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HIV-1 Envelope Conformation, Allostery, and Dynamics.
Bennett, Ashley Lauren; Henderson, Rory.
Affiliation
  • Bennett AL; Duke Human Vaccine Institute, Durham, NC 27710, USA.
  • Henderson R; Duke Human Vaccine Institute, Durham, NC 27710, USA.
Viruses ; 13(5)2021 05 07.
Article in En | MEDLINE | ID: mdl-34067073
ABSTRACT
The HIV-1 envelope glycoprotein (Env) mediates host cell fusion and is the primary target for HIV-1 vaccine design. The Env undergoes a series of functionally important conformational rearrangements upon engagement of its host cell receptor, CD4. As the sole target for broadly neutralizing antibodies, our understanding of these transitions plays a critical role in vaccine immunogen design. Here, we review available experimental data interrogating the HIV-1 Env conformation and detail computational efforts aimed at delineating the series of conformational changes connecting these rearrangements. These studies have provided a structural mapping of prefusion closed, open, and transition intermediate structures, the allosteric elements controlling rearrangements, and state-to-state transition dynamics. The combination of these investigations and innovations in molecular modeling set the stage for advanced studies examining rearrangements at greater spatial and temporal resolution.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: HIV Envelope Protein gp41 / HIV-1 / Env Gene Products, Human Immunodeficiency Virus Language: En Journal: Viruses Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: HIV Envelope Protein gp41 / HIV-1 / Env Gene Products, Human Immunodeficiency Virus Language: En Journal: Viruses Year: 2021 Document type: Article Affiliation country: