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High affinity type I interleukin 1 receptor antagonists discovered by screening recombinant peptide libraries.

Authors :
Yanofsky SD
Baldwin DN
Butler JH
Holden FR
Jacobs JW
Balasubramanian P
Chinn JP
Cwirla SE
Peters-Bhatt E
Whitehorn EA
Tate EH
Akeson A
Bowlin TL
Dower WJ
Barrett RW
Source :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 1996 Jul 09; Vol. 93 (14), pp. 7381-6.
Publication Year :
1996

Abstract

Two families of peptides that specifically bind the extracellular domain of the human type I interleukin I (IL-1) receptor were identified from recombinant peptide display libraries. Peptides from one of these families blocked binding of IL-lalpha to the type I IL-1 receptor with IC50 values of 45-140 microM. Affinity-selective screening of variants of these peptides produced ligands of much higher affinity (IC50 approximately 2 nM). These peptides block IL-1-driven responses in human and monkey cells; they do not bind the human type II IL-1 receptor or the murine type I IL-1 receptor. This is the first example (that we know of) of a high affinity peptide that binds to a cytokine receptor and acts as a cytokine antagonist.

Details

Language :
English
ISSN :
0027-8424
Volume :
93
Issue :
14
Database :
MEDLINE
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
8693002
Full Text :
https://doi.org/10.1073/pnas.93.14.7381