噬菌体展示
计算生物学
蛋白质微阵列
肽库
抗体
蛋白质组
DNA微阵列
蛋白质组学
抗原
蛋白质阵列分析
计算机科学
抗体微阵列
生物
生物信息学
遗传学
肽序列
基因
基因表达
作者
Anna Säll,Maria Walle,Christer Wingren,Susanne Müller,T. Nyman,Andrea Vala,Mats Ohlin,Carl Borrebaeck,Helena Persson
标识
DOI:10.1093/protein/gzw042
摘要
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.
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