Molecular Biology and Genetics
 

Biotechnology Industry

Electronic Journal of Biotechnology ISSN: 0717-3458 Vol. 13 No. 1, Issue of January 15, 2010
© 2010 by Pontificia Universidad Católica de Valparaíso -- Chile Received October 17, 2008 / Accepted August 4, 2009
DOI: 10.2225/vol13-issue1-fulltext-8
RESEARCH ARTICLE

Development of potency assays for a plasmid containing vascular endothelial growth factor 2

Li-chun Huang*
Corautus Genetics Inc.
500 Forbes Blvd.
South San Francisco, CA94555
San José. California, USA
E-mail: Lhuang2006@gmail.com

Emily Chin
Corautus Genetics Inc.
500 Forbes Blvd.
South San Francisco, CA94555
San José. California, USA 

Yawen L. Chiang
Corautus Genetics Inc.
500 Forbes Blvd.
South San Francisco, CA94555
San José. California, USA

*Corresponding author

Keywords: cell proliferation, plasmid DNA, potency assays, receptor binding, VEGF-2.

Abbreviations:

BrdU: 5-bromo-2’deoxyuridine
BSA: bovine serum albumin           
CHO: Chinese hamster ovary
HLMVEC: human lymph microvascular endothelial cells
PBS: phosphate buffered saline
RSD: relative standard deviation
VEGF: vascular endothelial growth factor
VEGFR: vascular endothelial growth factor receptor

Abstract   Full Text

We have developed analytical methods to measure the biological functions of pVGI.1(VEGF2), a naked plasmid DNA product containing vascular endothelial growth factor 2 used in clinical trials for coronary artery diseases (CAD) and peripheral artery diseases (PAD). After being injected into muscles, vascular endothelial growth factor 2 (VEGF-2), presumably expressed in muscle tissues, binds to the endothelial cell receptors VEGFR2 or VEGFR3, triggering the downstream responses including cell proliferation and vascularization. As it is important to make sure clinical material is biological active, we developed a quantitative assay first to measure the receptor binding activity of the pVGI.1(VEGF2) gene product expressed by the transfected host cells, and then a qualitative assay to confirm the cell proliferation promoting activity of the expressed protein. In both assays the signals were plotted directly against input DNA concentrations used to transfect the host cells. We confirmed specificity for both assays. In addition, we demonstrated acceptable levels of spike recovery (86.7-116%), precision (largest relative standard deviation (RSD)=19.3%), linearity and range (60-140% relative potency, 15 - 35 µg/mL) for the quantitative assay. We intend to use the potency assays for routine lot release and stability studies.

Supported by UNESCO / MIRCEN network