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

被引:98
作者
Yanofsky, SD
Baldwin, DN
Butler, JH
Holden, FR
Jacobs, JW
Balasubramanian, P
Chinn, JP
Cwirla, SE
PetersBhatt, E
Whitehorn, EA
Tate, EH
Akeson, A
Bowlin, TL
Dower, WJ
Barrett, RW
机构
[1] AFFYMAX RES INST,DEPT CHEM,PALO ALTO,CA 94304
[2] AFFYMAX RES INST,DEPT MOLEC BIOL,PALO ALTO,CA 94304
[3] HOECHST MARION ROUSSEL,DEPT IMMUNOL,CINCINNATI,OH 45215
关键词
D O I
10.1073/pnas.93.14.7381
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Two families of peptides that specifically bind the extracellular domain of the human type I interleukin 1 (IL-1) receptor were identified from recombinant peptide display libraries. Peptides from one of these families blocked binding of IL-1 alpha to the type I IL-1 receptor with IC50 values of 45-140 mu M. Affinity-selective screening of variants of these peptides produced ligands of much higher affinity (IC50 approximate to 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.
引用
收藏
页码:7381 / 7386
页数:6
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