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HIV-1 envelope glycoprotein gp120 V2 loop deleted mutant (Env gp120 ΔV2)

Target
Env gp120 ΔV2
Molecular classification
Viral envelope glycoprotein, Receptor-binding protein, Other (mutant protein)
01

Overview

The **HIV-1 envelope glycoprotein gp120 V2 loop deleted mutant** is a laboratory-engineered version of the gp120 subunit of the HIV-1 Env (envelope) glycoprotein in which the V2 variable loop sequence has been genetically removed. The gp120 protein normally mediates HIV-1 entry into host cells by binding to CD4 and a co-receptor (CCR5 or CXCR4), with the V2 loop playing a key role in masking critical conserved epitopes, contributing to immune evasion, and stabilizing trimeric Env structure. Deletion of the V2 loop results in increased exposure and accessibility of otherwise occluded neutralization epitopes, especially at the CD4 binding site and at specific regions of gp41. This makes the ΔV2 Env mutant a valuable tool in structural biology and HIV vaccine research (as an immunogen to elicit broader antibody responses), but the mutant is generally less stable and less efficient at mediating viral entry compared to wild-type Env. It is not itself a direct therapeutic target but is an important reagent for studying HIV Env biology and vaccine immunogen design[1][2][3][5][7].

Other names
gp120 V2-deleted mutantHIV-1 Env ΔV2gp120 ΔV2 mutant
02

Mechanism of action

Drugs or antibodies targeting this molecule inhibit HIV-1 entry by blocking receptor or co-receptor binding Broadly neutralizing antibodies bind newly exposed conserved sites when the V2 loop is deleted, enhancing neutralization

03

Biological functions

Viral entry into host cellsReceptor (CD4) and co-receptor (CCR5/CXCR4) bindingShielding of neutralizing antibody epitopesModulation of immune evasion
04

Disease associations

Infection (HIV/AIDS)Immune evasionVaccine antigen design (experimental)
05

Safety considerations

Altered immunogenicity (deletion increases exposure of conserved neutralizing epitopes, which may enhance immunogenicity, but may also destabilize the protein)Loss of structural integrity and function with extensive loop deletions[1][2]Decreased viral fitness in some backgrounds[7]Not a therapeutic target per se, but an engineered antigen for research/vaccine design
06

Interacting drugs

Broadly neutralizing antibodies (e.g., PG9, PG16, 2F5, 17b, 48d)

2 more in the full profile.

07

Biomarkers

Exposure of neutralizing antibody epitopes (such as CD4 binding site and V3 loop)Not routinely used as a clinical biomarker, but used in experimental immunogen design

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