Abstract:
:As antibody-based diagnosis and therapy grow at an increased pace, there is a need for methods which rapidly and accurately determine antibody-antigen interactions. Here, we report a method for the multiplex determination of antibody epitopes using bacterial cell-surface display. A protein-fragment library with 10(7) cell clones, covering 60 clinically-relevant protein targets, was created and characterized with massively parallel sequencing. Using this multi-target fragment library we determined simultaneously epitopes of commercial monoclonal and polyclonal antibodies targeting PSMA, EGFR, and VEGF. Off-target binding was observed for one of the antibodies, which demonstrates the methods ability to reveal cross-reactivity. We exemplify the detection of structural epitopes by mapping the therapeutic antibody Avastin. Based on our findings we suggest this method to be suitable for mapping linear and structural epitopes of monoclonal and polyclonal antibodies in a multiplex fashion and could find applicability in serum profiling as well as other protein-protein interaction studies.
journal_name
Sci Repjournal_title
Scientific reportsauthors
Hudson EP,Uhlen M,Rockberg Jdoi
10.1038/srep00706subject
Has Abstractpub_date
2012-01-01 00:00:00pages
706issn
2045-2322journal_volume
2pub_type
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journal_title:Scientific reports
pub_type: 杂志文章
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pub_type: 杂志文章
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pub_type: 杂志文章
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