The mixture of proteins secreted by neonatal rat aorta smooth muscle cells
cultured in the presence of beta-aminopropionitrile was readily oxidized an
d polymerized upon incubation with purified or crude preparations of lysyl
oxidase, Western blot analysis indicated that these substrates included 30-
60kDa protein bands reactive with anti-elastin, presumed to be fragments de
rived from tropoelastin, Thus, truncated, elastin-like as well as other pro
teins accumulate in the media of these cultures which, in toto, can serve a
s a conveniently prepared, highly efficient substrate for the routine assay
of lysyl oxidase activity.