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Efficient isolation of peptide ligands for the endothelial cell protein C receptor (EPCR) using candidate receptor phage display biopanning
被引:5
|作者:
White, SJ
Simmonds, RE
Lane, DA
Baker, AH
机构:
[1] Univ Bristol, Bristol Royal Infirm, Bristol Heart Inst, Bristol BS2 8HW, Avon, England
[2] Univ London Imperial Coll Sci & Technol, Fac Med, Dept Haematol, London W12 0NN, England
[3] Univ Glasgow, Dept Med & Therapeut, Glasgow G11 6NT, Lanark, Scotland
来源:
关键词:
endothelial cell protein C receptors;
EPCR;
peptide ligands;
phage display;
D O I:
10.1016/j.peptides.2005.01.015
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Phage display biopanning has been used for a number of applications including ligand generation for targeted drug delivery, targeting gene therapy vectors and identification of protein-protein interaction sites. In this study, a random phage display library was used to isolate peptide ligands to the endothelial protein C receptor (EPCR), identifying 74 different peptide sequences and several motifs. Binding to EPCR was characterized by a solid phase binding assay, demonstrating that 95 % of isolated peptides were specific for EPCR. Several homologies with potential relevance to EPCR biology were identified, the most notable being leukolysin (MT-MMP6) and cerastocytin. (c) 2005 Elsevier Inc. All rights reserved.
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页码:1264 / 1269
页数:6
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