Back to Search
Start Over
High affinity type I interleukin 1 receptor antagonists discovered by screening recombinant peptide libraries.
- 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.
- Subjects :
- Animals
Base Sequence
Binding, Competitive
Cell Line
Cells, Cultured
DNA Primers
Databases, Factual
Dinoprostone metabolism
ErbB Receptors biosynthesis
Escherichia coli
Haplorhini
Humans
Interleukin-1 pharmacology
Kinetics
Male
Mice
Molecular Sequence Data
Peptides chemical synthesis
Polymerase Chain Reaction
Radioligand Assay
Receptors, Interleukin-1 biosynthesis
Recombinant Fusion Proteins antagonists & inhibitors
Recombinant Fusion Proteins biosynthesis
Skin drug effects
Skin immunology
Skin metabolism
Spleen immunology
Interleukin-1 metabolism
Peptides chemistry
Peptides pharmacology
Receptors, Interleukin-1 antagonists & inhibitors
Subjects
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