Replacing Antibodies: Engineering New Binding Proteins

被引:65
作者
Banta, Scott [1 ]
Dooley, Kevin [1 ]
Shur, Oren [1 ]
机构
[1] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
来源
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, VOL 15 | 2013年 / 15卷
关键词
protein scaffolds; antibody alternatives; molecular imaging; bispecific proteins; biosensors; DESIGNING REPEAT PROTEINS; LEUCINE-RICH REPEAT; DIRECTED EVOLUTION; PHAGE DISPLAY; BISPECIFIC ANTIBODIES; GROWTH-FACTOR; IN-VITRO; COMBINATORIAL LIBRARIES; COMPUTATIONAL DESIGN; PICOMOLAR AFFINITY;
D O I
10.1146/annurev-bioeng-071812-152412
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Nature's reliance on proteins to carry out nearly all biological processes has led to the evolution of biomolecules that exhibit a seemingly endless range of functions. Much research has been devoted toward advancing this process in the laboratory in order to create new proteins with improved or unique capabilities. The protein-engineering field has rapidly evolved from pioneering studies in engineering protein stability and activity to an application-driven powerhouse on the forefront of emerging technologies in biomedical engineering and biotechnology. A classic protein-engineering technique in the medical field has focused on manipulating antibodies and antibody fragments for various applications. New classes of alternative scaffolds have recently challenged this paradigm, and these structures have been successfully engineered for applications including targeted cancer therapy, regulated drug delivery, in vivo imaging, and a host of others. This review aims to capture recent advances in the engineering of nonimmunoglobulin scaffolds as well as some of the applications for these molecular recognition elements in the biomedical field.
引用
收藏
页码:93 / 113
页数:21
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