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Engineered high-affinity nanobodies recognizing staphylococcal Protein A and suitable for native isolation of protein complexes.
Fridy, Peter C; Thompson, Mary K; Ketaren, Natalia E; Rout, Michael P.
Afiliación
  • Fridy PC; Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, NY 10065, USA.
  • Thompson MK; Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, NY 10065, USA.
  • Ketaren NE; Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, NY 10065, USA.
  • Rout MP; Laboratory of Cellular and Structural Biology, The Rockefeller University, New York, NY 10065, USA. Electronic address: rout@rockefeller.edu.
Anal Biochem ; 477: 92-4, 2015 May 15.
Article en En | MEDLINE | ID: mdl-25707320
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteína Estafilocócica A / Ingeniería de Proteínas / Anticuerpos de Dominio Único Tipo de estudio: Prognostic_studies Idioma: En Revista: Anal Biochem Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteína Estafilocócica A / Ingeniería de Proteínas / Anticuerpos de Dominio Único Tipo de estudio: Prognostic_studies Idioma: En Revista: Anal Biochem Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos