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Effects of fibronectin-type V collagen recombinant fusion protein on cell adhesion and cell proliferation.

作者信息

Hatai M, Takahara K, Hashi H, Kato I, Yaoi Y

机构信息

Biology Division, National Cancer Center Research Institute, Tokyo, Japan.

出版信息

Cell Struct Funct. 1992 Oct;17(5):293-300. doi: 10.1247/csf.17.293.

DOI:10.1247/csf.17.293
PMID:1473159
Abstract

An expression vector pTF7520-Col-V-In, which encodes a fusion protein of the cell-binding domain of fibronectin (C277) and the insulin- and heparin-binding domain of the alpha 1 chain of human type V collagen, was constructed. E. coli transfected with this plasmid synthesized a 50-kDa fusion protein. This fusion protein, C277-V, was purified from the crude extract by a single step heparin HPLC. Similar amounts of insulin bound to purified C277-V and to the alpha 1 chain of type V collagen as judged by the binding of peroxidase-conjugated insulin. Cell-adhesive activity of C277-V was lower than that of the original fibronectin fragment C274, but similar numbers of cells adhered to both protein substrates when the culture dishes were coated with 1 mM of each protein. Insulin bound to the C277-V substratum stimulated the growth of mouse mammary tumor MTD cells in serum-free culture medium.

摘要

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