Host Cell Protein Profiling in Biopharmaceutical Harvests

被引:9
作者
Obrstar, Darja [1 ]
Kroener, Frieder [2 ]
Japelj, Bostjan [1 ]
Bojic, Lea [1 ]
Anderka, Oliver [2 ]
机构
[1] Novartis Pharma AG, Kolodvorska 27, SI-1234 Menges, Slovenia
[2] Novartis Pharma AG, Klybeckstr 141, CH-4057 Basel, Switzerland
关键词
DIFFERENCE GEL-ELECTROPHORESIS; PROTEOMIC ANALYSIS; RECOVERY; PRODUCTS;
D O I
10.1021/acs.analchem.8b01236
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Biopharmaceuticals contain residual host cell protein (HCP) impurities, a complex mixture of endogenous proteins from production cell lines such as Chinese hamster ovary (CHO) cells. The composition of HCP impurities at harvest hinges on multiple factors, e.g., identity of cell line, cell density and viability at harvest, or other process parameters. Two-dimensional differential gel electrophoresis (2-D DIGE) was used to compare HCP in 15 null cell culture harvest supernatants, which are representative for a wide range of manufacturing processes of therapeutic antibodies, using five different CHO cell lines. Numerical metrics were developed to quantitatively compare HCP composition, which may be used to assess the suitability of a platform HCP assay standard for a new product or to assess the impact of process changes. A very similar HCP composition was found for the 15 analyzed CHO null cell culture harvests, demonstrating that even the wide range of applied manufacturing processes did not have a strong influence on the HCP impurities.
引用
收藏
页码:11240 / 11247
页数:8
相关论文
共 23 条
  • [1] A novel experimental design for comparative two-dimensional gel analysis: Two-dimensional difference gel electrophoresis incorporating a pooled internal standard
    Alban, A
    David, SO
    Bjorkesten, L
    Andersson, C
    Sloge, E
    Lewis, S
    Currie, I
    [J]. PROTEOMICS, 2003, 3 (01) : 36 - 44
  • [2] State of the art of 2D DIGE
    Arentz, Georgia
    Weiland, Florian
    Oehler, Martin K.
    Hoffmann, Peter
    [J]. PROTEOMICS CLINICAL APPLICATIONS, 2015, 9 (3-4) : 277 - 288
  • [3] Champion KM, 2001, PROTEOMICS, V1, P1133, DOI 10.1002/1615-9861(200109)1:9<1133::AID-PROT1133>3.0.CO
  • [4] 2-S
  • [5] Responses of CHO cell lines to increased pCO2 at normal (37°C) and reduced (33°C) culture temperatures
    Darja, Obrstar
    Stanislav, Mandelc
    Sasa, Stojkovic
    Andrej, Francky
    Lea, Bojic
    Branka, Javornik
    [J]. JOURNAL OF BIOTECHNOLOGY, 2016, 219 : 98 - 109
  • [6] Host cell proteins in biotechnology-derived products: A risk assessment framework
    de Zafra, Christina L. Zuch
    Quarmby, Valerie
    Francissen, Kathleen
    Vanderlaan, Martin
    Zhu-Shimoni, Judith
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2015, 112 (11) : 2284 - 2291
  • [7] 2-D DIGE to expedite downstream process development for human monoclonal antibody purification
    Grzeskowiak, Julita K.
    Tscheliessnig, Anne
    Toh, Poh Choo
    Chusainow, Janet
    Lee, Yih Yean
    Wong, Niki
    Jungbauer, Alois
    [J]. PROTEIN EXPRESSION AND PURIFICATION, 2009, 66 (01) : 58 - 65
  • [8] Profiling of Host Cell Proteins by Two-Dimensional Difference Gel Electrophoresis (2D-DIGE): Implications for Downstream Process Development
    Jin, Mi
    Szapiel, Nicolas
    Zhang, Jennifer
    Hickey, John
    Ghose, Sanchayita
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2010, 105 (02) : 306 - 316
  • [9] Proteomic studies support the use of multi-product immunoassays to monitor host cell protein impurities
    Krawitz, DC
    Forrest, W
    Moreno, GT
    Kittleson, J
    Champion, KM
    [J]. PROTEOMICS, 2006, 6 (01) : 94 - 110
  • [10] Recovery and purification process development for monoclonal antibody production
    Liu, Hui F.
    Ma, Junfen
    Winter, Charles
    Bayer, Robert
    [J]. MABS, 2010, 2 (05) : 480 - 499