Dual-Site Target Molecule Detection for Higher Selectivity

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Solution Overview

Problem

Existing target molecule detection methods, such as ELISA and those disclosed in JP 2023-160814 A, lack sufficient selectivity for detecting target molecules due to the first and second capture substances binding to the same site, leading to reduced specificity and sensitivity.

Innovation Solution

A target molecule detection kit and method utilizing a first binding element immobilized on a solid phase with reaction specificity to a first specific binding site and a second binding element connected to a label generating a detection signal with reaction specificity to a second specific binding site, ensuring high selectivity by binding to different sites on the target molecule.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Device complexity

If the first and second capture substances bind to the same site on the target substance, then the detection process is simplified, but the selectivity for the target substance is reduced

Engineering Contradiction:
Improvedetection process complexityVSAvoidselectivity for target substance
Core Design Contradiction:
Device complexityVSMeasurement precision

Solution Approach 1:

The patent divides the binding interaction into two separate segments: the first capture substance binds to a first binding site on the target substance, while the second capture substance binds to a second binding site. This segmentation ensures that both capture substances can simultaneously bind to the target without competing for the same site, thereby maintaining high selectivity while enabling a straightforward detection process.

Inventive Principle:
Principle #1Segmentation

2Ease of manufacture

If the first capture substance is used to fix the target substance and the second capture substance is used to detect the target substance, then the detection method is established, but high selectivity cannot be ensured when both bind to the same site

Engineering Contradiction:
Improvedetection method establishmentVSAvoidselectivity for target substance
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent applies local quality by assigning different binding specificities to different parts of the detection system. The first capture substance is designed with specificity for a first binding site, while the second capture substance is designed with specificity for a second binding site. This local differentiation ensures that each component performs its function with high selectivity, preventing cross-competition and ensuring reliable target substance detection.

Inventive Principle:
Principle #3Local quality

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 method enables easier and more accurate detection of target molecules with enhanced selectivity and sensitivity, allowing for precise quantification and differentiation from non-target molecules.

Implementation Method 1

a second binding element connected to a label capable of generating a detection signal through a chemical reaction

Methodology Applied
Scientific EffectChemical reaction: Chemical Bonding

Data Source

PatentEP4667937A1Target molecule detection kit and target molecule detection method
Publication Date: 2025.12.24 DENSO CORP
  • EP4667937A1 patent drawingFigure 1~2
  • EP4667937A1 patent drawingFigure 3~4
  • EP4667937A1 patent drawingFigure 5~6

AI summary

A target molecule detection kit used to detect a target molecule (10) includes a first binding element (20) and a second binding element (40). The first binding element is immobilized on a solid phase (30). The first binding element has reaction specificity to a first specific binding site of the target molecule. The second binding element is connected to a label (50) that generates a detection signal. The second binding element having reaction specificity to a second specific binding site of the target molecule that is different from the first specific binding site.