Adnectins: engineered target-binding protein therapeutics

被引:193
作者
Lipovsek, D. [1 ]
机构
[1] Adnexus, Dept Prot Design, Waltham, MA 02453 USA
关键词
(10)Fn3; Adnectin; Engineered therapeutic proteins; mRNA display; PROfusion; MESSENGER-RNA DISPLAY; GROWTH-FACTOR RECEPTOR-2; YEAST SURFACE DISPLAY; HIGH-AFFINITY; III DOMAIN; HUMAN FIBRONECTIN; MOLECULAR RECOGNITION; CRYSTAL-STRUCTURE; RIBOSOME DISPLAY; BINARY-CODE;
D O I
10.1093/protein/gzq097
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
Adnectins(TM) are a new family of therapeutic proteins based on the 10th fibronectin type III domain, and designed to bind with high affinity and specificity to therapeutically relevant targets. Adnectins share with antibody variable domains a beta-sheet sandwich fold with diversified loops, but differ from antibodies in primary sequence and have a simpler, single-domain structure without disulfide bonds. As a consequence, Adnectins bind targets with affinity and specificity as high as those of antibodies, but are easier to manipulate genetically and compatible with bacterial expression systems. Adnectins that bind macromolecular targets with nanomolar and picomolar affinity have been selected using in vitro evolution methods, including mRNA display, phage display and yeast display. CT-322, a PEGylated, anti-angiogenic Adnectin that binds vascular endothelial growth factor (VEGF) receptor 2 and blocks its interaction with VEGF A, C and D, is being evaluated in Phase II clinical trials for efficacy in several oncology indications.
引用
收藏
页码:3 / 9
页数:7
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