2. Academic Validation
  3. Targeted Capture of Chinese Hamster Ovary Host Cell Proteins: Peptide Ligand Discovery

Targeted Capture of Chinese Hamster Ovary Host Cell Proteins: Peptide Ligand Discovery

  • Int J Mol Sci. 2019 Apr 8;20(7):1729. doi: 10.3390/ijms20071729.
R Ashton Lavoie 1,  Alice di Fazio 2,  R Kevin Blackburn 3,  Michael B Goshe 4,  Ruben G Carbonell 5 6 7,  Stefano Menegatti 8 9
Affiliations

Affiliations

  • 1 Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, USA. rabradl3@ncsu.edu.
  • 2 Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, USA. abdifazi@ncsu.edu.
  • 3 Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC 27695-7622, USA. Kevin_Blackburn@waters.com.
  • 4 Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, NC 27695-7622, USA. mbgoshe@ncsu.edu.
  • 5 Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, USA. ruben@ncsu.edu.
  • 6 Biomanufacturing Training and Education Center (BTEC), North Carolina State University, Raleigh, NC 27695-7905, USA. ruben@ncsu.edu.
  • 7 National Institute for Innovation in Manufacturing Biopharmaceuticals (NIIMBL), Newark, DE 19711, USA. ruben@ncsu.edu.
  • 8 Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, USA. smenega@ncsu.edu.
  • 9 Biomanufacturing Training and Education Center (BTEC), North Carolina State University, Raleigh, NC 27695-7905, USA. smenega@ncsu.edu.
PMID: 30965558 DOI: 10.3390/ijms20071729
Abstract

The growing integration of quality-by-design (QbD) concepts in biomanufacturing calls for a detailed and quantitative knowledge of the profile of impurities and their impact on the product safety and efficacy. Particularly valuable is the determination of the residual level of host cell proteins (HCPs) secreted, together with the product of interest, by the recombinant cells utilized for production. Though often referred to as a single impurity, HCPs comprise a variety of species with diverse abundance, size, function, and composition. The clearance of these impurities is a complex issue due to their cell line to cell line, product-to-product, and batch-to-batch variations. Improvements in HCP monitoring through proteomic-based methods have led to identification of a subset of "problematic" HCPs that are particularly challenging to remove, both at the product capture and product polishing steps, and compromise product stability and safety even at trace concentrations. This paper describes the development of synthetic peptide ligands capable of capturing a broad spectrum of Chinese hamster ovary (CHO) HCPs with a combination of peptide species that allow for advanced mixed-mode binding. Solid phase peptide libraries were screened for identification and characterization of Peptides that capture CHO HCPs while showing minimal binding of human IgG, utilized here as a model product. Tetrameric and hexameric ligands featuring either multipolar or hydrophobic/positive amino acid compositions were found to be the most effective. Tetrameric multipolar ligands exhibited the highest targeted binding ratio (ratio of HCP clearance over IgG loss), more than double that of commercial mixed-mode and anion exchange resins utilized by industry for IgG polishing. All peptide resins tested showed preferential binding to HCPs compared to IgG, indicating potential uses in flow-through mode or weak-partitioning-mode chromatography.

Keywords

host cell proteins; peptide ligands; protein purification; therapeutic antibodies.

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