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• W2768275428 endingPage "463" @default.
• W2768275428 startingPage "456" @default.
• W2768275428 abstract "In this work, we report the development of a general strategy for enhancing the efficiency of target capture in immunoassays, using a bifunctional fusion protein construct which incorporates a substrate-anchoring moiety for the high-abundance immobilization of an antigen-binding domain. This approach was informed by the development of a pseudo first-order rate constant model, and tested in a paper-based assay format using a fusion construct consisting of an rcSso7d binding module and a cellulose-binding domain. These rcSso7d-CBD fusion proteins were solubly expressed and purified from bacteria in high molar yields, and enable oriented, high-density adsorption of the rcSso7d binding species to unmodified cellulose within a 30-second incubation period. These findings were validated using two distinct, antigen-specific rcSso7d variants, which were isolated from a yeast surface display library via flow cytometry. Up to 1.6 micromoles of rcSso7d-CBD was found to adsorb per gram of cellulose, yielding a volume-averaged binder concentration of up to 760 μM within the resulting active material. At this molar abundance, the target antigen is captured from solution with nearly 100% efficiency, maximizing the attainable sensitivity for any given diagnostic system." @default.
• W2768275428 created "2017-12-04" @default.
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• W2768275428 date "2018-04-01" @default.
• W2768275428 modified "2023-10-14" @default.
• W2768275428 title "Paper-based diagnostics in the antigen-depletion regime: High-density immobilization of rcSso7d-cellulose-binding domain fusion proteins for efficient target capture" @default.
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• W2768275428 doi "https://doi.org/10.1016/j.bios.2017.11.050" @default.
• W2768275428 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5983361" @default.
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• W2768275428 hasPublicationYear "2018" @default.
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