| Literature DB >> 25707320 |
Peter C Fridy1, Mary K Thompson1, Natalia E Ketaren1, Michael P Rout2.
Abstract
In addition to its high affinity for antibody Fc domains, staphylococcal Protein A has been shown to bind certain Fab domains. We investigated this in order to develop a small, recombinant Protein A-binding alternative to immunoglobulin G (IgG) from nanobodies, single-domain antibodies derived from a camelid variant IgG's variable region. We engineered a nanobody with affinity solely for Protein A as well as a dimerized version of higher affinity for typical multidomain Protein A constructs. Because this recombinant nanobody can be immobilized using a cleavable crosslinker, it has proven to be suitable for the isolation and mild elution of protein complexes in native conditions.Entities:
Keywords: Affinity isolation; Immunoprecipitation; Nanobody; Native elution; Protein A (PrA)
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Year: 2015 PMID: 25707320 PMCID: PMC4404190 DOI: 10.1016/j.ab.2015.02.013
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365