Automated Screening Procedure for High-Throughput Generation of Antibody Fragments

In the emerging field of proteomics, there is an urgent need for catcher molecules such as antibodies for detecting the proteome or parts of the proteome in a microarray format. A suitable source for providing a large diversity of binders is obtained by combinatorial libraries, such as phage display...

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Bibliographic Details
Published inBioTechniques Vol. 33; no. S6; pp. S30 - S37
Main Authors Hallborn, Johan, Carlsson, Roland
Format Journal Article
LanguageEnglish
Published England Future Science Ltd 01.12.2002
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Summary:In the emerging field of proteomics, there is an urgent need for catcher molecules such as antibodies for detecting the proteome or parts of the proteome in a microarray format. A suitable source for providing a large diversity of binders is obtained by combinatorial libraries, such as phage display libraries of single chain antibody fragments (scFv) or Fab fragments. To find novel binders from the n-CoDeR libraries with a high throughput, we have automated the screening process with robotics. The automated system is configured to screen tens of thousands of clones per day to target antigens in various formats, including peptides and soluble proteins, as well as cell-bound targets; thus, it is well designed to meet demands from the proteomics area.
ISSN:0736-6205
1940-9818
DOI:10.2144/dec02-hallborn