Abstract

BackgroundThe HIV-1 Env glycoprotein mediates virus entry by catalyzing direct fusion between the virion membrane and the target cell plasma membrane. Env is composed of two subunits: gp120, which binds to CD4 and the coreceptor, and gp41, which is triggered upon coreceptor binding to promote the membrane fusion reaction. Env on the surface of infected cells is a trimer consisting of three gp120/gp41 homo-dimeric protomers. An emerging question concerns cooperative interactions between the protomers in the trimer, and possible implications for Env function.ResultsWe extended studies on cooperative subunit interactions within the HIV-1 Env trimer, using analysis of functional complementation between coexpressed inactive variants harboring different functional deficiencies. In assays of Env-mediated cell fusion, complementation was observed between variants with a wide range of defects in both the gp120 and gp41 subunits. The former included gp120 subunits mutated in the CD4 binding site or incapable of coreceptor interaction due either to mismatched specificity or V3 loop mutation. Defective gp41 variants included point mutations at different residues within the fusion peptide or heptad repeat regions, as well as constructs with modifications or deletions of the membrane proximal tryptophan-rich region or the transmembrane domain. Complementation required the defective variants to be coexpressed in the same cell. The observed complementation activities were highly dependent on the assay system. The most robust activities were obtained with a vaccinia virus-based expression and reporter gene activation assay for cell fusion. In an alternative system involving Env expression from integrated provirus, complementation was detected in cell fusion assays, but not in virus particle entry assays.ConclusionOur results indicate that Env function does not require every subunit in the trimer to be competent for all essential activities. Through cross-talk between subunits, the functional determinants on one defective protomer can cooperatively interact to trigger the functional determinants on an adjacent protomer(s) harboring a different defect, leading to fusion. Cooperative subunit interaction is a general feature of the Env trimer, based on complementation activities observed for a highly diverse range of functional defects.

Highlights

  • The human immunodeficiency virus (HIV)-1 envelope glycoprotein (Env) glycoprotein mediates virus entry by catalyzing direct fusion between the virion membrane and the target cell plasma membrane

  • We show that subunit complementation is a general capacity of the human immunodeficiency virus type 1 (HIV-1) Env trimer, though its efficiency and detectability are dependent on the particular defective variants examined and the assay systems employed

  • We examined complementation between variants in gp120 that were inactive due to inability to interact with CD4 (CD4 CD4 binding site (BS) mutation) or coreceptor, as well as variants in gp41 with mutations at different points within the fusion peptide (FP) and HR1 regions, as well as modifications of the membrane proximal tryptophan-rich region (TRR) and the transmembrane (TM) domain (Fig. 1)

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Summary

Introduction

The HIV-1 Env glycoprotein mediates virus entry by catalyzing direct fusion between the virion membrane and the target cell plasma membrane. Env-mediated fusion involves a strict division of labor between the two subunits: gp120 is responsible for sequential binding to specific target cell receptors, first to CD4 and to the coreceptor (a specific chemokine receptor, typically CCR5 or CXCR4); receptor binding triggers gp to promote membrane fusion. These steps involve a tightly orchestrated series of conformational changes in both Env subunits that drive the fusion process. The heptad repeat (HR) segments near the external C-terminal region (HR2) fold to insert in anti-parallel fashion into the grooves formed by the cluster of the three N-terminal heptad repeat (HR1) segments; the resulting formation of a 6-

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