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Quantification of a Non-conventional Protein Secretion: The Low-Molecular-Weight FGF-2 Example
Tania Arcondéguy1, Christian Touriol1, Eric Lacazette2
1Centre de Recherches en Cancérologie de Toulouse - CRCT UMR1037 Inserm/Université Toulouse III Paul Sabatier ERL5294 CNRS, Oncopole de Toulouse 2 Avenue, Hubert Curien, CS 53717, 31037, Toulouse Cedex 1, France.
Abstract:
Quantification of secreted factors is most often measured with enzyme-linked immunosorbent assay (ELISA), Western Blot, or more recently with antibody arrays. However, some of these, like low-molecular-weight fibroblast growth factor-2 (LMW FGF-2; the 18 kDa form), exemplify a set of secreted but almost non-diffusible molecular actors. It has been proposed that phosphorylated FGF-2 is secreted via a non-vesicular mechanism and that heparan sulfate proteoglycans function as extracellular reservoir but also as actors for its secretion. Heparan sulfate is a linear sulfated polysaccharide present on proteoglycans found in the extracellular matrix or anchored in the plasma membrane (syndecan). Moreover the LMW FGF-2 secretion appears to be activated upon FGF-1 treatment. In order to estimate quantification of such factor export across the plasma membrane, technical approaches are presented (evaluation of LMW FGF-2: (1) secretion, (2) extracellular matrix reservoir, and (3) secretion modulation by surrounding factors) and the importance of such procedures in the comprehension of the biology of these growth factors is underlined.

