c-Met Targeting Peptide Composition for Solubility and Affinity

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Solution Overview

Problem

Existing peptides targeting c-Met suffer from poor water solubility and limited affinity, hindering their clinical application in cancer therapy and diagnosis.

Innovation Solution

Development of peptides with improved water solubility and affinity to c-Met, formulated as specific sequences and derivatives, which can be conjugated with drugs for targeted delivery to cancer cells.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If existing peptides targeting c-Met are used, then they can bind to c-Met protein, but they exhibit poor water solubility and limited affinity

Engineering Contradiction:
Improvebinding affinity to c-MetVSAvoidwater solubility
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The patent modifies the peptide structure by changing amino acid sequences and introducing specific chemical modifications (such as N-terminal acetylation, C-terminal amide, and side-chain modifications) to improve both water solubility and binding affinity simultaneously. This resolves the contradiction by optimizing molecular parameters rather than accepting the trade-off between solubility and affinity.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates composite peptide structures by combining hydrophilic and hydrophobic amino acid residues in specific arrangements, and by conjugating peptides with drugs or imaging agents. This composite approach allows the peptide to maintain both good water solubility and high binding affinity to c-Met.

Inventive Principle:
Principle #40Composite materials

2Ease of manufacture

If existing peptides targeting c-Met are used, then they can be synthesized, but they require improved affinity and solubility for clinical application

Engineering Contradiction:
Improvesynthesis capabilityVSAvoidclinical therapeutic efficacy
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent optimizes peptide parameters including molecular weight, charge distribution, and hydrophilicity-hydrophobicity balance to achieve both ease of synthesis and high clinical efficacy. The modified sequences maintain simplicity for synthesis while dramatically improving binding affinity and solubility for therapeutic use.

Inventive Principle:
Principle #35Parameter changes

3Object-affected harmful factors

If targeted drugs are used to treat cancer, then they can reduce damage to normal tissues, but existing c-Met targeting peptides have limited effectiveness due to poor solubility and affinity

Engineering Contradiction:
Improvedamage to normal tissuesVSAvoidtherapeutic effect
Core Design Contradiction:
Object-affected harmful factorsVSReliability

Solution Approach 1:

By optimizing the peptide's physical-chemical parameters (solubility, stability, binding affinity), the patent ensures that the targeted drug can effectively reach and bind to c-Met on cancer cells, thereby achieving both reduced damage to normal tissues and high therapeutic efficacy.

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentEP4725955A1Peptide targeting c-met, pharmaceutical composition comprising said peptide and use thereof
Publication Date: 2026.04.15 NANJING ANJI BIOLOGICAL TECH CO LTD
  • EP4725955A1 patent drawingFigure 1~2A
  • EP4725955A1 patent drawingFigure 2A
  • EP4725955A1 patent drawingFigure 2B

AI summary

A peptide targeting c-Met, derivatives thereof, a pharmaceutical composition and drug-peptide conjugate comprising the peptide or the derivatives thereof, and the use of same in the detection, prevention or treatment of diseases (e.g., cancers). In addition, the peptide or the derivatives thereof can increase the water solubility of a drug.