Jf. Clemence et al., PHOTOIMMOBILIZATION OF A BIOACTIVE LAMININ FRAGMENT AND PATTERN-GUIDED SELECTIVE NEURONAL CELL ATTACHMENT, Bioconjugate chemistry, 6(4), 1995, pp. 411-417
To attain light-dependent functionalization of biocompatible materials
, a photolabel-derivatized, bioactive laminin fragment has been synthe
sized, chemically characterized, and photoimmobilized. Covalent high-r
esolution patterning of the laminin fragment CDPGYIGSR to hydroxylated
fluorinated ethylene propylene (FEP-OH), poly(vinyl alcohol), and gly
cophase glass has been achieved. The synthetic peptide CDPGYIGSR was t
hermochemically coupled to either methyl)diazirin-3-yl]phenyl]-4-malei
midobutyramide or 4-maleimidobenzophenone. Photolabel-derivatized pept
ides were radiolabeled, and 20 and 300 mu m-sized patterns were visual
ized by autoradiography. The biospecific interaction of photoimmobiliz
ed laminin fragments with cells was investigated by analyzing the sele
ctive attachment of NG 108-15 neuroblastoma x glioma cells which bear
CDPGYIGSR-specific cell surface receptors. On photopatterned FEP-OH me
mbranes NG 108-15 cells differentiated in serum-supplemented media wit
hin 1 day. Specific attachment to the immobilized oligopeptide CDPGYIG
SR was assessed in serum-free media with competitive binding studies,
showing an 82% decrease in cell adherence after the cell receptors wer
e blocked with soluble CDPGYIGSR.