| Literature DB >> 27933702 |
Jinpeng Wang1, Jingwen Yu1, Qin Yang1, John McDermott1, Alexander Scott1, Matthew Vukovich1, Remy Lagrois1, Qiang Gong1, William Greenleaf2, Michael Eisenstein3, B Scott Ferguson1, H Tom Soh3.
Abstract
Aptamers are a promising class of affinity reagents because they are chemically synthesized, thus making them highly reproducible and distributable as sequence information rather than a physical entity. Although many high-quality aptamers have been previously reported, it is difficult to routinely generate aptamers that possess both high affinity and specificity. One of the reasons is that conventional aptamer selection can only be performed either for affinity (positive selection) or for specificity (negative selection), but not both simultaneously. In this work, we harness the capacity of fluorescence activated cell sorting (FACS) for multicolor sorting to simultaneously screen for affinity and specificity at a throughput of 107 aptamers per hour. As a proof of principle, we generated DNA aptamers that exhibit picomolar to low nanomolar affinity in human serum for three diverse proteins, and show that these aptamers are capable of outperforming high-quality monoclonal antibodies in a standard ELISA detection assay.Entities:
Keywords: affinity reagents; aptamers; flow cytometry; high-throughput screening; molecular recognition
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Year: 2016 PMID: 27933702 PMCID: PMC5225111 DOI: 10.1002/anie.201608880
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336