Activated Carbon Fragment Removal in Protein Purification

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current protein purification processes, particularly for monoclonal antibodies, struggle to effectively remove protein fragments that share similar properties with the intact protein, leading to impurities in the final product.

Innovation Solution

The use of activated carbon to bind and remove protein fragments from a sample containing a target protein, increasing the purity of the target protein by selectively adsorbing fragments without affecting the intact protein.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional purification steps (clarification, affinity chromatography, ion exchange chromatography) are used, then the target protein is purified from cells, cell debris, DNA, and host cell proteins, but protein fragments that share similar properties with the intact protein remain as impurities

Engineering Contradiction:
Improvepurification effectivenessVSAvoidfragment removal efficiency
Core Design Contradiction:
ReliabilityVSManufacturing precision

Solution Approach 1:

The patent applies parameter changes by adjusting pH and ionic strength conditions to optimize the binding of protein fragments to activated carbon while maintaining intact protein in solution. By controlling solution conditions, the method achieves selective removal of fragments without affecting the target protein

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses activated carbon, a cost-effective and readily available material, to remove protein fragments. Activated carbon serves as a disposable adsorbent that can be easily removed from the solution after binding fragments, providing an economical solution to the fragment removal problem

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

2Manufacturing precision

If activated carbon is used to remove protein fragments, then fragment removal efficiency increases significantly, but there is a risk of also adsorbing the intact target protein

Engineering Contradiction:
Improvefragment removal efficiencyVSAvoidtarget protein recovery
Core Design Contradiction:
Manufacturing precisionVSReliability

Solution Approach 1:

The patent carefully controls pH and ionic strength parameters to create conditions where protein fragments bind to activated carbon while the intact target protein remains in solution. This parameter optimization ensures high fragment removal efficiency while maintaining target protein recovery

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses controlled amounts of activated carbon and limited contact times to achieve partial adsorption - specifically targeting fragments while avoiding excessive adsorption of the intact protein. This controlled partial action prevents loss of target protein

Inventive Principle:
Principle #16Partial or excessive action

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

Activated carbon significantly reduces the amount of protein fragments in the sample, enhancing the purity of the target protein by up to 90% or more, making it suitable for therapeutic proteins requiring regulatory approval.

Implementation Method 1

contacting the sample with activated carbon; wherein the activated carbon binds the fragments

Methodology Applied
Scientific EffectAdsorption: Adsorption

Data Source

PatentUS10519194B2Removal of fragments from a sample containing a target protein using activated carbon
Publication Date: 2019.12.31 MERCK PATENT GMBH
  • US10519194B2 patent drawing
  • US10519194B2 patent drawing
  • US10519194B2 patent drawing

AI summary

The present invention provides novel and improved protein purification processes which incorporate certain types of carbonaceous materials and result in effective and selective removal, of protein, fragments without adversely affecting the yield of the desired protein product.