Abstract
Antibody-based proteomics offers distinct advantages in the analysis of complex samples for discovery and validation of biomarkers associated with disease. However, its large-scale implementation requires tools and technologies that allow development of suitable antibody or antibody fragments in a high-throughput manner. To address this we designed and constructed two human synthetic antibody fragment (scFv) libraries denoted HelL-11 and HelL-13. By the use of phage display technology, in total 466 unique scFv antibodies specific for 114 different antigens were generated. The specificities of these antibodies were analyzed in a variety of immunochemical assays and a subset was further evaluated for functionality in protein microarray applications. This high-throughput approach demonstrates the ability to rapidly generate a wealth of reagents not only for proteome research, but potentially also for diagnostics and therapeutics. In addition, this work provides a great example on how a synthetic approach can be used to optimize library designs. By having precise control of the diversity introduced into the antigen-binding sites, synthetic libraries offer increased understanding of how different diversity contributes to antibody binding reactivity and stability, thereby providing the key to future library optimization.
Original language | English |
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Pages (from-to) | 427-437 |
Number of pages | 11 |
Journal | Protein Engineering Design & Selection |
Volume | 29 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2016 Oct 1 |
Subject classification (UKÄ)
- Medical Biotechnology
Free keywords
- affinity proteomics
- phage display technology
- protein microarrays
- scFv
- synthetic antibody libraries
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Unit for Rapid Engineered Antibody Development
Ohlin, M. (Manager)
Department of ImmunotechnologyInfrastructure