DESIGN AND SYNTHESIS OF A MIMETIC FROM AN ANTIBODY COMPLEMENTARITY-DETERMINING REGION

被引:152
作者
SARAGOVI, HU
FITZPATRICK, D
RAKTABUTR, A
NAKANISHI, H
KAHN, M
GREENE, MI
机构
[1] UNIV PENN, SCH MED, DEPT PATHOL & LAB MED, PHILADELPHIA, PA 19104 USA
[2] UNIV ILLINOIS, DEPT CHEM, CHICAGO, IL 60680 USA
关键词
D O I
10.1126/science.1876837
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
A technique for producing non-peptide compounds (mimetics) of designed specificities was developed that permitted the synthesis of a conformationally restricted molecule that mimicked the binding and functional properties of monoclonal antibody (MAb) 87.92.6, which recognizes the reovirus type 3 cellular receptor. Binding of either MAb 87.92.6, peptide analogs, or 87.1-mimetic to the cellular receptor inhibited cellular proliferation. The mimetic was a synthetic beta-loop structure that mimics the second complementarity-determining region of the MAb. These studies may lead to strategies for the synthetic design of antibody complementarity regions, ligands, and other pharmacologically active agents that are water soluble, resistant to proteolysis, and nonimmunogenic.
引用
收藏
页码:792 / 795
页数:4
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