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Photochemical surface derivatization of a peptide containing Arg-Gly-Asp (RGD)

✍ Scribed by Sugawara, Takashi ;Matsuda, Takehisa


Book ID
102876650
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
659 KB
Volume
29
Category
Article
ISSN
0021-9304

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✦ Synopsis


Abstract

A photoreactive octapeptide (Gly–Gly–Gly–Arg–Gly–Asp–Ser–Pro), into which the cell adhesive tripeptidyl sequence Arg–Gly–Asp (RGD) was incorporated, was derivatized with 4‐azidobenzoyloxysuccinimide at its N‐terminal. Photochemical surface immobilization of the RGD peptide on poly (vinyl alcohol) (PVA) was performed by adsorption and subsequent ultraviolet (UV) irradiation and was evidenced by electron spectra for chemical analysis (ESCA) measurements. Bovine endothelial cells (ECs) adhered and spread well on the RGD peptide‐derivatized surfaces in a biologically specific manner. The use of a photomask during UV irradiation enabled preparation of a two‐dimensional tissue with micron‐order precision. Thus surface immobilization of a photoreactive, cell‐adhesive peptide easily can create a cell attachment surface at a desired portion or region of a polymer surface or device. © 1995 John Wiley & Sons, Inc.


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We have synthesized a new compound in which Arg-Gly-Asp-Ser (RGDS) was conjugated with 6-O-sulfated and 6-O-carboxymethyl-chitin (SCM-chitin), i.e. SCM-chitin-RGDS, and tested the inhibitory effect on lung and liver metastases of three different types of tumors in mice. SCM-chitin-RGDS was more effe