Release of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins

ABSTRACT Primary human immunodeficiency virus (HIV-1) envelope glycoprotein (Env) trimers [(gp120/gp41)3] typically exist in a metastable closed conformation (state 1). Binding the CD4 receptor triggers Env to undergo extensive conformational changes to mediate virus entry. We identified specific gp...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Alon Herschhorn, Xiaochu Ma, Christopher Gu, John D. Ventura, Luis Castillo-Menendez, Bruno Melillo, Daniel S. Terry, Amos B. Smith, Scott C. Blanchard, James B. Munro, Walther Mothes, Andrés Finzi, Joseph Sodroski
Formato: article
Lenguaje:EN
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://doaj.org/article/554073aa2fb04b81baef67f9a2afc910
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:554073aa2fb04b81baef67f9a2afc910
record_format dspace
spelling oai:doaj.org-article:554073aa2fb04b81baef67f9a2afc9102021-11-15T15:50:14ZRelease of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins10.1128/mBio.01598-162150-7511https://doaj.org/article/554073aa2fb04b81baef67f9a2afc9102016-11-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01598-16https://doaj.org/toc/2150-7511ABSTRACT Primary human immunodeficiency virus (HIV-1) envelope glycoprotein (Env) trimers [(gp120/gp41)3] typically exist in a metastable closed conformation (state 1). Binding the CD4 receptor triggers Env to undergo extensive conformational changes to mediate virus entry. We identified specific gp120 residues that restrain Env in state 1. Alteration of these restraining residues destabilized state 1, allowing Env to populate a functional conformation (state 2) intermediate between state 1 and the full CD4-bound state (state 3). Increased state 2 occupancy was associated with lower energy barriers between the states. State 2 was an obligate intermediate for all transitions between state 1 and state 3. State 2-enriched Envs required lower CD4 concentrations to trigger virus entry and more efficiently infected cells expressing low levels of CD4. These Envs were resistant to several broadly neutralizing antibodies and small-molecule inhibitors. Thus, state 2 is an Env conformation on the virus entry pathway; sampling state 2 increases the adaptability of HIV-1 to different host cell receptor levels and immune environments. Our results provide new insights into the conformational regulation of HIV-1 entry. IMPORTANCE The envelope glycoproteins (Env) of HIV-1 mediate virus entry and are the sole targets of neutralizing antibodies. Understanding the way that Env promotes HIV-1 entry can expedite drug and vaccine development. By destabilizing Env, we found that it assumes an intermediate state that is functional and obligate for transitions to entry-competent conformations. Increased sampling of this state enhances the ability of HIV-1 to infect cells that express low levels of the CD4 receptor and allows the virus to evade neutralizing antibodies and small-molecule inhibitors. These findings provide new mechanistic insights into the function and inhibition of HIV-1 Env and will contribute to ongoing therapeutic and prevention efforts to combat HIV-1.Alon HerschhornXiaochu MaChristopher GuJohn D. VenturaLuis Castillo-MenendezBruno MelilloDaniel S. TerryAmos B. SmithScott C. BlanchardJames B. MunroWalther MothesAndrés FinziJoseph SodroskiAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 7, Iss 5 (2016)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Alon Herschhorn
Xiaochu Ma
Christopher Gu
John D. Ventura
Luis Castillo-Menendez
Bruno Melillo
Daniel S. Terry
Amos B. Smith
Scott C. Blanchard
James B. Munro
Walther Mothes
Andrés Finzi
Joseph Sodroski
Release of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins
description ABSTRACT Primary human immunodeficiency virus (HIV-1) envelope glycoprotein (Env) trimers [(gp120/gp41)3] typically exist in a metastable closed conformation (state 1). Binding the CD4 receptor triggers Env to undergo extensive conformational changes to mediate virus entry. We identified specific gp120 residues that restrain Env in state 1. Alteration of these restraining residues destabilized state 1, allowing Env to populate a functional conformation (state 2) intermediate between state 1 and the full CD4-bound state (state 3). Increased state 2 occupancy was associated with lower energy barriers between the states. State 2 was an obligate intermediate for all transitions between state 1 and state 3. State 2-enriched Envs required lower CD4 concentrations to trigger virus entry and more efficiently infected cells expressing low levels of CD4. These Envs were resistant to several broadly neutralizing antibodies and small-molecule inhibitors. Thus, state 2 is an Env conformation on the virus entry pathway; sampling state 2 increases the adaptability of HIV-1 to different host cell receptor levels and immune environments. Our results provide new insights into the conformational regulation of HIV-1 entry. IMPORTANCE The envelope glycoproteins (Env) of HIV-1 mediate virus entry and are the sole targets of neutralizing antibodies. Understanding the way that Env promotes HIV-1 entry can expedite drug and vaccine development. By destabilizing Env, we found that it assumes an intermediate state that is functional and obligate for transitions to entry-competent conformations. Increased sampling of this state enhances the ability of HIV-1 to infect cells that express low levels of the CD4 receptor and allows the virus to evade neutralizing antibodies and small-molecule inhibitors. These findings provide new mechanistic insights into the function and inhibition of HIV-1 Env and will contribute to ongoing therapeutic and prevention efforts to combat HIV-1.
format article
author Alon Herschhorn
Xiaochu Ma
Christopher Gu
John D. Ventura
Luis Castillo-Menendez
Bruno Melillo
Daniel S. Terry
Amos B. Smith
Scott C. Blanchard
James B. Munro
Walther Mothes
Andrés Finzi
Joseph Sodroski
author_facet Alon Herschhorn
Xiaochu Ma
Christopher Gu
John D. Ventura
Luis Castillo-Menendez
Bruno Melillo
Daniel S. Terry
Amos B. Smith
Scott C. Blanchard
James B. Munro
Walther Mothes
Andrés Finzi
Joseph Sodroski
author_sort Alon Herschhorn
title Release of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins
title_short Release of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins
title_full Release of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins
title_fullStr Release of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins
title_full_unstemmed Release of gp120 Restraints Leads to an Entry-Competent Intermediate State of the HIV-1 Envelope Glycoproteins
title_sort release of gp120 restraints leads to an entry-competent intermediate state of the hiv-1 envelope glycoproteins
publisher American Society for Microbiology
publishDate 2016
url https://doaj.org/article/554073aa2fb04b81baef67f9a2afc910
work_keys_str_mv AT alonherschhorn releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT xiaochuma releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT christophergu releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT johndventura releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT luiscastillomenendez releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT brunomelillo releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT danielsterry releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT amosbsmith releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT scottcblanchard releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT jamesbmunro releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT walthermothes releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT andresfinzi releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
AT josephsodroski releaseofgp120restraintsleadstoanentrycompetentintermediatestateofthehiv1envelopeglycoproteins
_version_ 1718427457987543040