Blocking monocyte transmigration in in vitro system by a human antibody scFv anti-CD99. Efficient large scale purification from periplasmic inclusion bodies in E. coli expression system

Diego Moricoli*, William Anthony Muller, Damiano Cosimo Carbonella, Maria Cristina Balducci, Sabrina Dominici, Richard Watson, Valentina Fiori, Evan Weber, Maurizio Cianfriglia, Katia Scotlandi, Mauro Magnani

*Corresponding author for this work

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

Migration of leukocytes into site of inflammation involves several steps mediated by various families of adhesion molecules. CD99 play a significant role in transendothelial migration (TEM) of leukocytes. Inhibition of TEM by specific monoclonal antibody (mAb) can provide a potent therapeutic approach to treating inflammatory conditions. However, the therapeutic utilization of whole IgG can lead to an inappropriate activation of Fc receptor-expressing cells, inducing serious adverse side effects due to cytokine release. In this regard, specific recombinant antibody in single chain variable fragments (scFvs) originated by phage library may offer a solution by affecting TEM function in a safe clinical context. However, this consideration requires large scale production of functional scFv antibodies and the absence of toxic reagents utilized for solubilization and refolding step of inclusion bodies that may discourage industrial application of these antibody fragments. In order to apply the scFv anti-CD99 named C7A in a clinical setting, we herein describe an efficient and large scale production of the antibody fragments expressed in E. coli as periplasmic insoluble protein avoiding gel filtration chromatography approach, and laborious refolding step pre- and post-purification. Using differential salt elution which is a simple, reproducible and effective procedure we are able to separate scFv in monomer format from aggregates. The purified scFv antibody C7A exhibits inhibitory activity comparable to an antagonistic conventional mAb, thus providing an excellent agent for blocking CD99 signaling. This protocol can be useful for the successful purification of other monomeric scFvs which are expressed as periplasmic inclusion bodies in bacterial systems.

Original languageEnglish (US)
Pages (from-to)35-45
Number of pages11
JournalJournal of Immunological Methods
Volume408
DOIs
StatePublished - Jun 2014

Keywords

  • Aggregates
  • Blocking monocyte transmigration
  • Periplasmic inclusion bodies
  • Purification
  • Single chain variable fragment (scFv)

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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