Multivalent Display of Single-Domain Antibodies
Antigen-binding fragments, such as single-domain antibodies (sdAbs), can now be readily isolated by in vitro technologies. Antibody fragment libraries derived from immune or nonimmune sources are presented in a molecular display format, typically phage display, and binders to individual antigens are selected from the libraries by a so-called panning process. Nonimmune libraries can serve as sources of binders to a wide range of targets but yield antigen-binding fragments that generally have much lower affinities than those obtained from immune sources. Here we describe a strategy for constructing pentameric sdAbs termed pentabodies. Pentamerization introduces avidity which can greatly enhance the binding of low affinity sdAbs to antigens presented on surfaces.
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Multivalent Protein Probes for the Identification and Characterization of Cognate Cellular Ligands f
Cell–cell interactions mediated by cell surface receptor–lig...
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Multiplexed Flow Cytometry: High-Throughput Screening of Single-Chain Antibodies
The development of high-throughput screening (HTS) technolog...