Recombinant gp36 Antigen Design for Sensitive HIV-2 Antibody Detection

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Solution Overview

Problem

The hydrophobic nature of the HIV gp36 protein makes it difficult to prepare products with good detection performance for HIV-2 antibody detection.

Innovation Solution

A recombinant antigen based on a gp36 protein sequence (SEQ ID NO: 1) is used, which can include specific segments of the gp36 protein and may have cysteine mutations, fused with a fusion partner, and conjugated with a tracer marker or solid-phase carrier, within a reagent/kit for HIV detection.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If the gp36 protein is used directly for HIV-2 antibody detection, then the detection target is covered, but the hydrophobic nature of the protein makes it difficult to prepare products with good detection performance

Engineering Contradiction:
Improvedetection performanceVSAvoidproduct preparation difficulty
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The gp36 protein is divided into multiple epitope segments (first epitope, second epitope, third epitope) that are then combined in different configurations to create multiple recombinant antigens. This segmentation allows the hydrophobic protein to be broken into manageable pieces that can be effectively used in detection while maintaining the necessary immunogenicity.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Multiple epitope segments from the gp36 protein are combined to form composite recombinant antigens with different structures and properties. These composite antigens (with varying epitope combinations) provide diverse detection capabilities that overcome the limitations of using the complete hydrophobic gp36 protein directly.

Inventive Principle:
Principle #40Composite materials

2Measurement precision

If multiple recombinant antigens with different epitope combinations are prepared, then detection coverage and performance are improved, but the complexity of antigen preparation increases

Engineering Contradiction:
Improvedetection sensitivity and specificityVSAvoidantigen preparation complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The gp36 protein is divided into multiple epitope segments (first epitope, second epitope, third epitope) that can be independently combined. This segmentation creates a modular system where different epitope combinations can be systematically prepared to achieve comprehensive detection coverage while maintaining organized preparation procedures.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The multiple recombinant antigens with different epitope combinations serve multiple detection purposes simultaneously. Each antigen configuration targets different aspects of HIV-2 antibody detection, providing universal coverage across various detection scenarios and improving overall detection reliability without requiring entirely separate preparation protocols.

Inventive Principle:
Principle #6Universality (Multi-functionality)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The recombinant antigen achieves high sensitivity and specificity in detecting HIV-2 antibodies, with improved thermal stability through cysteine mutations, and can be used in immunoassays like ELISA and colloidal gold immunochromatography.

Implementation Method 1

The recombinant antigen achieves high sensitivity and specificity in detecting HIV-2 antibodies

Methodology Applied
Scientific EffectAntigen-antibody binding:

Data Source

PatentEP4714965A1Recombinant antigen for detecting HIV antibody
Publication Date: 2026.03.25 FAPON BIOTECH INC
  • EP4714965A1 patent drawingFigure 1
  • EP4714965A1 patent drawing
  • EP4714965A1 patent drawing

AI summary

Provided is an HIV recombinant antigen for detecting an HIV antibody, which belongs to the technical field of immunodiagnosis. The present application specifically relates to an HIV recombinant antigen, a nucleic acid molecule, an expression vector, a host cell, a reagent, a kit, and uses thereof. In the present invention, the recombinant HIV antigen protein is used in a label end, which can significantly improve the marker activity of the recombinant HIV antigen, reduce non-specific immune binding activity, and enhance sensitivity.