Chimeric Polypeptides for S. aureus Vaccine Development

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Solution Overview

Problem

Current methods for developing vaccines against Staphylococcus aureus are time-consuming, labor-intensive, and often ineffective due to limitations in culturing microorganisms and identifying protective antigens.

Innovation Solution

The development of novel recombinant chimeric polypeptides and polynucleotides derived from Staphylococcus aureus, which can be used as immunogens to induce protective immunity against S. aureus infections.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If traditional empirical approach is used for subunit vaccine development, then vaccine development can be pursued, but the process is time-consuming and labor-intensive

Engineering Contradiction:
Improvevaccine development efficiencyVSAvoidtime for antigen identification and purification
Core Design Contradiction:
ProductivityVSLoss of time

Solution Approach 1:

The patent applies preliminary action by using computational methods and bioinformatics tools to predict and identify protective antigens before actual vaccine development. The system pre-processes genomic data, predicts antigenic properties, and screens for candidate proteins in advance, thereby avoiding time-consuming empirical testing of numerous proteins and significantly accelerating the vaccine development process.

Inventive Principle:
Principle #10Preliminary action

2Productivity

If traditional empirical approach is used for subunit vaccine development, then vaccine development can be pursued, but the process is labor-intensive and expensive

Engineering Contradiction:
Improvevaccine development efficiencyVSAvoidamount of proteins required for testing
Core Design Contradiction:
ProductivityVSQuantity of substance

Solution Approach 1:

The patent applies copying by using computational models and digital representations of proteins and genomic data instead of physically handling and testing large quantities of actual proteins. The system creates virtual models of bacterial proteins, predicts their immunogenicity through computer algorithms, and screens candidates in silico, thereby eliminating the need to produce and test extensive protein libraries and significantly reducing material requirements and costs.

Inventive Principle:
Principle #26Copying

3Measurement precision

If traditional empirical approach is used, then antigen identification can be performed, but protective antigens are difficult to identify among abundant proteins

Engineering Contradiction:
Improveaccuracy of protective antigen identificationVSAvoiddifficulty in finding protective antigens in protein sea
Core Design Contradiction:
Measurement precisionVSDifficulty of detecting and measuring

Solution Approach 1:

The patent applies local quality by focusing computational analysis on specific regions and properties of proteins that are likely to be protective. The system evaluates local characteristics such as surface accessibility, conservation across strains, and specific structural motifs that are indicative of protective antigens, rather than uniformly analyzing all proteins. This targeted approach enables precise identification of protective antigens by examining their local functional properties and distinguishing them from abundant non-protective proteins.

Inventive Principle:
Principle #3Local quality

Data Source

PatentUS12209110B2Chimeric proteins for inducing immunity towards infection with <i>S. aureus</i>
Publication Date: 2025.01.28 EVAXION BIOTECH A/S
  • US12209110B2 patent drawing
  • US12209110B2 patent drawing
  • US12209110B2 patent drawing

AI summary

Disclosed is chimeric polypeptides derived from S. aureus proteins having SEQ ID NOs: 1-9 and 139-146. The chimeric polypeptides are useful as immunogens for providing protective immunity against S. aureus infection. Also disclosed are compositions, methods of treatment and prophylaxis, nucleic acids and vectors comprising the nucleic acids.