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 |
|---|---|
| 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 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Subject classification (UKÄ)
- Medical Biotechnology
Free keywords
- affinity proteomics
- phage display technology
- protein microarrays
- scFv
- synthetic antibody libraries
Fingerprint
Dive into the research topics of 'Generation and analyses of human synthetic antibody libraries and their application for protein microarrays'. Together they form a unique fingerprint.Infrastructure
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Unit for Rapid Engineered Antibody Development
Ohlin, M. (Manager)
Department of ImmunotechnologyInfrastructure
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