Literature DB >> 25534831

Use of the site-specific retargeting jump-in platform cell line to support biologic drug discovery.

Robin Butler1, David Hornigold2, Ling Huang3, Catherine Huntington3, Tim London3, Janette Dillon3, Natalie J Tigue3, Alessandra Rossi2, Jacqueline Naylor2, Trevor Wilkinson3.   

Abstract

Biologics represent a fast-growing class of therapeutics in the pharmaceutical sector. Discovery of therapeutic antibodies and characterization of peptides can necessitate high expression of the target gene requiring the generation of clonal stably transfected cell lines. Traditional challenges of stable cell line transfection include gene silencing and cell-to-cell variability. Our inability to control these can present challenges in lead isolation. Recent progress in site-specific targeting of transgene to specific genomic loci has transformed the ability to generate stably transfected mammalian cell lines. In this article, we describe how the use of the Jump-In platform (Life Technologies, Carlsbad, CA) has been applied to drug discovery projects. It can easily and rapidly generate homogeneous high-expressing cell pools with a high degree of reproducibility. Their use in cell-based screening to identify specific binders, identify binding to relevant species variants, or detect functionally relevant therapeutic antibodies is central in driving drug discovery.
© 2014 Society for Laboratory Automation and Screening.

Entities:  

Keywords:  cell based assays; cell line development; drug discovery; site-specific integration

Mesh:

Year:  2014        PMID: 25534831     DOI: 10.1177/1087057114562715

Source DB:  PubMed          Journal:  J Biomol Screen        ISSN: 1087-0571


  5 in total

1.  Automated Acoustic Dispensing for the Serial Dilution of Peptide Agonists in Potency Determination Assays.

Authors:  Jacqueline Naylor; Alessandra Rossi; Christopher Brankin; David C Hornigold
Journal:  J Vis Exp       Date:  2016-11-10       Impact factor: 1.355

2.  Controlling the bioactivity of a peptide hormone in vivo by reversible self-assembly.

Authors:  Myriam M Ouberai; Ana L Gomes Dos Santos; Sonja Kinna; Shimona Madalli; David C Hornigold; David Baker; Jacqueline Naylor; Laura Sheldrake; Dominic J Corkill; John Hood; Paolo Vicini; Shahid Uddin; Steven Bishop; Paul G Varley; Mark E Welland
Journal:  Nat Commun       Date:  2017-10-18       Impact factor: 14.919

3.  A GLP-1:CCK fusion peptide harnesses the synergistic effects on metabolism of CCK-1 and GLP-1 receptor agonism in mice.

Authors:  David C Hornigold; Emma Roth; Victor Howard; Sarah Will; Stephanie Oldham; Matthew P Coghlan; Clemence Blouet; James L Trevaskis
Journal:  Appetite       Date:  2018-05-19       Impact factor: 3.868

4.  Robust anti-obesity and metabolic effects of a dual GLP-1/glucagon receptor peptide agonist in rodents and non-human primates.

Authors:  S J Henderson; A Konkar; D C Hornigold; J L Trevaskis; R Jackson; M Fritsch Fredin; R Jansson-Löfmark; J Naylor; A Rossi; M A Bednarek; N Bhagroo; H Salari; S Will; S Oldham; G Hansen; M Feigh; T Klein; J Grimsby; S Maguire; L Jermutus; C M Rondinone; M P Coghlan
Journal:  Diabetes Obes Metab       Date:  2016-08-15       Impact factor: 6.577

5.  Development and characterisation of a novel glucagon like peptide-1 receptor antibody.

Authors:  Emma K Biggs; Lihuan Liang; Jacqueline Naylor; Shimona Madalli; Rachel Collier; Matthew P Coghlan; David J Baker; David C Hornigold; Peter Ravn; Frank Reimann; Fiona M Gribble
Journal:  Diabetologia       Date:  2017-11-09       Impact factor: 10.122

  5 in total

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