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Highly efficient production of anti-HER2 scFv antibody variant for targeting breast cancer cells

TitoloHighly efficient production of anti-HER2 scFv antibody variant for targeting breast cancer cells
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2011
AutoriSommaruga, S., Lombardi Alessio, Salvadè A., Mazzucchelli S., Corsi F., Galeffi Patrizia, Tortora P., and Prosperi D.
RivistaApplied Microbiology and Biotechnology
Paginazione1 - 9
Data di pubblicazione2011///
Parole chiaveBreast cancer, HER2, Pichia pastoris, Single-chain variable fragment antibody
Abstract

The human epidermal growth factor receptor 2 (HER2) is a transmembrane tyrosine kinase receptor overexpressed in 30% of human breast cancers. One of the mechanisms by which tumor cell proliferation can be inhibited consists in hampering HER2 dimerization by targeting its extracellular domain with specific antibodies. In recent clinical practice, a valuable alternative to entire IgGs resides in the use of smaller molecules, such as single-chain variable fragments (scFv), developed for selective molecular targeting. In this paper, we report on the production and purification of a soluble anti-HER2 scFv antibody secreted by Pichia pastoris. The gene encoding scFv800E6 with an additional 6× His-tag at the 3'-end was inserted into the expression vector pPICZα and transformed in P. pastoris. The highest expression level was obtained in presence of 0.5% methanol and 0.8% glycerol in the culture medium after 48 h of induction. The use of P. pastoris proved very valuable as an expression system, allowing the isolation of 10 mg/L of highly purified antibody, remarkably higher than previously reported data. The functionality of purified anti-HER2 scFv was assessed by cytofluorimetry and immunofluorescence on HER2-positive MCF7 breast cancer cells, showing good affinity and high selectivity for the target membrane receptor. These findings confirm that P. pastoris is a suitable host for high level expression of antibody fragments and highlight the potential role of scFv800E6 in diagnostic and therapeutic application. © 2011 Springer-Verlag.

Note

Export Date: 16 June 2011Source: ScopusArticle in Press

URLhttp://www.scopus.com/inward/record.url?eid=2-s2.0-79955460014&partnerID=40&md5=738184ce702bde24298c23d93ae9667a
Citation Key1883