Discovery of Novel Candidate Therapeutics and Diagnostics Based on Engineered Human Antibody Domains

Author(s): Weizao Chen, Rui Gong, Tianlei Ying, Ponraj Prabakaran, Zhongyu Zhu, Yang Feng, Dimiter S. Dimitrov

Journal Name: Current Drug Discovery Technologies

Volume 11 , Issue 1 , 2014

Become EABM
Become Reviewer
Call for Editor


The smallest independently folded antibody fragments, the domains, are emerging as promising scaffolds for candidate therapeutics and diagnostics that bind specifically targets of interest. The discovery of such binders is based on several technologies including structure-based design and generation of libraries of mutants displayed on phage or yeast, next-generation sequencing for diversity analysis, panning and screening of the libraries, affinity maturation of selected binders, and their expression, purification, and characterization for specific binding, function, and aggregation propensity. In this review, we describe these technologies as applied for the generation of engineered antibody domains (eAds), especially those derived from the human immunoglobulin heavy chain variable region (VH) and the second domain of IgG1 heavy chain constant region (CH2) as potential candidate therapeutics and diagnostics, and discuss examples of eAds against HIV-1 and cancer-related proteins.

Keywords: Antibody domains, human, library, phage display, scaffold, stability, therapeutics, yeast display.

promotion: free to download

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2014
Published on: 24 January, 2014
Page: [28 - 40]
Pages: 13
DOI: 10.2174/15701638113109990032

Article Metrics

PDF: 139