A V3 loop-dependent gp120 element disrupted by CD4 binding stabilizes the human immunodeficiency virus envelope glycoprotein trimer

Shi Hua Xiang, Andrés Finzi, Beatriz Pacheco, Kevin Alexander, Wen Yuan, Carlo Rizzuto, Chih Chin Huang, Peter D. Kwong, Joseph Sodroski

Research output: Contribution to journalArticle

56 Citations (Scopus)

Abstract

Human immunodeficiency virus (HIV-1) entry into cells is mediated by a trimeric complex consisting of noncovalently associated gp120 (exterior) and gp41 (transmembrane) envelope glycoproteins. The binding of gp120 to receptors on the target cell alters the gp120-gp41 relationship and activates the membrane-fusing capacity of gp41. Interaction of gp120 with the primary receptor, CD4, results in the exposure of the gp120 third variable (V3) loop, which contributes to binding the CCR5 or CXCR4 chemokine receptors. We show here that insertions in the V3 stem or polar substitutions in a conserved hydrophobic patch near the V3 tip result in decreased gp120-gp41 association (in the unliganded state) and decreased chemokine receptor binding (in the CD4-bound state). Subunit association and syncytium-forming ability of the envelope glycoproteins from primary HIV-1 isolates were disrupted more by V3 changes than those of laboratory-adapted HIV-1 envelope glycoproteins. Changes in the gp120 β2, β19, β20, and β21 strands, which evidence suggests are proximal to the V3 loop in unliganded gp120, also resulted in decreased gp120-gp41 association. Thus, a gp120 element composed of the V3 loop and adjacent beta strands contributes to quaternary interactions that stabilize the unliganded trimer. CD4 binding dismantles this element, altering the gp120-gp41 relationship and rendering the hydrophobic patch in the V3 tip available for chemokine receptor binding.

Original languageEnglish (US)
Pages (from-to)3147-3161
Number of pages15
JournalJournal of virology
Volume84
Issue number7
DOIs
StatePublished - Apr 1 2010

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Human immunodeficiency virus
Human immunodeficiency virus 1
HIV-1
glycoproteins
Chemokine Receptors
Glycoproteins
HIV
receptors
rendering
giant cells
CXCR4 Receptors
CD4 Antigens
Giant Cells
cells
stems
Membranes
chemokine receptors

ASJC Scopus subject areas

  • Microbiology
  • Immunology
  • Insect Science
  • Virology

Cite this

A V3 loop-dependent gp120 element disrupted by CD4 binding stabilizes the human immunodeficiency virus envelope glycoprotein trimer. / Xiang, Shi Hua; Finzi, Andrés; Pacheco, Beatriz; Alexander, Kevin; Yuan, Wen; Rizzuto, Carlo; Huang, Chih Chin; Kwong, Peter D.; Sodroski, Joseph.

In: Journal of virology, Vol. 84, No. 7, 01.04.2010, p. 3147-3161.

Research output: Contribution to journalArticle

Xiang, SH, Finzi, A, Pacheco, B, Alexander, K, Yuan, W, Rizzuto, C, Huang, CC, Kwong, PD & Sodroski, J 2010, 'A V3 loop-dependent gp120 element disrupted by CD4 binding stabilizes the human immunodeficiency virus envelope glycoprotein trimer', Journal of virology, vol. 84, no. 7, pp. 3147-3161. https://doi.org/10.1128/JVI.02587-09
Xiang, Shi Hua ; Finzi, Andrés ; Pacheco, Beatriz ; Alexander, Kevin ; Yuan, Wen ; Rizzuto, Carlo ; Huang, Chih Chin ; Kwong, Peter D. ; Sodroski, Joseph. / A V3 loop-dependent gp120 element disrupted by CD4 binding stabilizes the human immunodeficiency virus envelope glycoprotein trimer. In: Journal of virology. 2010 ; Vol. 84, No. 7. pp. 3147-3161.
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