Chimeric Peptides Inhibit JNK Signaling for Cystitis Treatment

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Solution Overview

Problem

Current JNK signaling pathway inhibitors are limited in their application to only a few diseases, and there is a need for new JNK inhibitor peptides that can target a broader range of diseases related to JNK signaling, including cystitis.

Innovation Solution

Development of chimeric peptides comprising a trafficking sequence and a JNK inhibitor sequence, specifically designed to inhibit JNK signaling pathway, which can be administered intravesically for treating cystitis and other inflammatory or non-inflammatory diseases related to JNK signaling.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If existing JNK signaling pathway inhibitors are used, then JNK activity is inhibited, but the application is limited to only a few diseases

Engineering Contradiction:
Improvedisease application rangeVSAvoidinhibition effectiveness
Core Design Contradiction:
Adaptability or versatilityVSReliability

Solution Approach 1:

The patent develops chimeric peptides that can inhibit JNK signaling pathway across multiple disease types including cystitis, neurological disorders, and inflammatory conditions. The peptides are designed with universal applicability to various JNK-related pathologies while maintaining reliable inhibition through optimized peptide sequences and structures

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

2Adaptability or versatility

If new JNK inhibitor peptides are developed for broader disease treatment, then disease coverage is expanded, but the number of known effective inhibitors increases

Engineering Contradiction:
Improvedisease coverageVSAvoidinhibitor variety
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent segments the JNK inhibitor development into specific chimeric peptide designs with defined sequences and structures. Each peptide is engineered as a discrete molecular entity with specific amino acid compositions, allowing systematic exploration of different inhibitor types while maintaining manageable complexity through structured design approaches

Inventive Principle:
Principle #1Segmentation

3Ease of operation

If chimeric peptides with trafficking sequences are designed, then cell permeability is improved, but peptide structure complexity increases

Engineering Contradiction:
Improvecell permeabilityVSAvoidpeptide structure
Core Design Contradiction:
Ease of operationVSDevice complexity

Solution Approach 1:

The patent merges the JNK inhibitor sequence with a trafficking sequence to create a single chimeric peptide molecule. This combination allows the peptide to simultaneously inhibit JNK signaling and penetrate cell membranes, achieving both therapeutic function and cellular delivery in one integrated structure

Inventive Principle:
Principle #5Merging (Combining)

4Reliability

If intravesical administration is used for cystitis treatment, then local efficacy is improved, but systemic availability is reduced

Engineering Contradiction:
Improvelocal treatment efficacyVSAvoidsystemic distribution
Core Design Contradiction:
ReliabilityVSQuantity of substance

Solution Approach 1:

The patent applies intravesical administration to deliver the chimeric peptide directly to the bladder tissue where cystitis occurs. This local delivery approach concentrates the therapeutic agent at the site of infection, maximizing local efficacy while minimizing systemic exposure and potential side effects

Inventive Principle:
Principle #3Local quality

Data Source

PatentEP3160489B9Cell-permeable peptide inhibitors of the JNK signal transduction pathway for the treatment of cystitis
Publication Date: 2023.10.04 XIGEN INFLAMMATION LTD
  • EP3160489B9 patent drawingFigure 1A~1C
  • EP3160489B9 patent drawingFigure 2
  • EP3160489B9 patent drawingFigure 3a~3d

AI summary

The present invention refers to the use of protein kinase inhibitors and more specifically to the use of inhibitors of the protein kinase c-Jun amino terminal kinase, JNK inhibitor sequences, chimeric peptides, or of nucleic acids encoding same as well as pharmaceutical compositions containing same, for the treatment of various diseases or disorders strongly related to JNK signaling.