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Structural Characterization of Monoclonal Antibodies and Epitope Mapping by FFAP Footprinting.
Fojtík, Lukás; Kalaninová, Zuzana; Fiala, Jan; Halada, Petr; Chmelík, Josef; Man, Petr; Kukacka, Zdenek; Novák, Petr.
Afiliación
  • Fojtík L; Institute of Microbiology of the Czech Academy of Sciences, Prague 142 20, Czech Republic.
  • Kalaninová Z; Faculty of Science, Charles University in Prague, Prague 128 00, Czech Republic.
  • Fiala J; Institute of Microbiology of the Czech Academy of Sciences, Prague 142 20, Czech Republic.
  • Halada P; Faculty of Science, Charles University in Prague, Prague 128 00, Czech Republic.
  • Chmelík J; Institute of Microbiology of the Czech Academy of Sciences, Prague 142 20, Czech Republic.
  • Man P; Institute of Microbiology of the Czech Academy of Sciences, Prague 142 20, Czech Republic.
  • Kukacka Z; Institute of Microbiology of the Czech Academy of Sciences, Prague 142 20, Czech Republic.
  • Novák P; Institute of Microbiology of the Czech Academy of Sciences, Prague 142 20, Czech Republic.
Anal Chem ; 96(19): 7386-7393, 2024 05 14.
Article en En | MEDLINE | ID: mdl-38698660
ABSTRACT
Covalent labeling in combination with mass spectrometry is a powerful approach used in structural biology to study protein structures, interactions, and dynamics. Recently, the toolbox of covalent labeling techniques has been expanded with fast fluoroalkylation of proteins (FFAP). FFAP is a novel radical labeling method that utilizes fluoroalkyl radicals generated from hypervalent Togni reagents for targeting aromatic residues. This report further demonstrates the benefits of FFAP as a new method for structural characterization of therapeutic antibodies and interaction interfaces of antigen-antibody complexes. The results obtained from human trastuzumab and its complex with human epidermal growth factor receptor 2 (HER2) correlate well with previously published structural data and demonstrate the potential of FFAP in structural biology.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Receptor ErbB-2 / Mapeo Epitopo / Trastuzumab Límite: Humans Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: República Checa

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Receptor ErbB-2 / Mapeo Epitopo / Trastuzumab Límite: Humans Idioma: En Revista: Anal Chem Año: 2024 Tipo del documento: Article País de afiliación: República Checa