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Construction of a divalent cell adhesive lysozyme by introducing the Arg‐Gly‐Asp sequence at two sites
Author(s) -
Yamada Takao,
Shimada Yoshimi,
Uyeda Atsuko,
Sugiyama Shigeru,
Kikuchi Masakazu
Publication year - 1995
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/0014-5793(95)01123-v
Subject(s) - lysozyme , divalent , sequence (biology) , chemistry , peptide sequence , adhesive , biochemistry , stereochemistry , organic chemistry , gene , layer (electronics)
To increase the cell adhesion activity of 74RGD4, an RGDS‐inserted mutant between Val 74 and Asn 75 of human lysozyme, one more site for the RGD introduction was investigated in the lysozyme molecule. We found that 47RGD4 with RGDS in place of AGDR (residues 47 to 50) in a β‐turn region possesses the same level of adhesion activity as that of 74RGD4. The acceptance of the RGD introduction in the β‐turn region of human lysozyme is in good agreement with recent studies on the functional conformation of RGD. We constructed (47,74)RGD4, a mutant containing RGD at two sites, by combining the N‐terminal domain of 47RGD4 and the C‐terminal domain of 74RGD4. The (47,74)RGD4 lysozyme, with two functional RGD sequences, exhibits even higher cell adhesion activity than that of 74RGD4 or 47RGD4.